University College London - Equipment Account

Lead Research Organisation: University College London
Department Name: Office of Vice Provost Research

Abstract

Catalysis is a core area of contemporary science posing major fundamental and conceptual challenges, while being at the heart of the chemical industry - an immensely successful and important part of the overall UK economy (generating in excess of £50 billion per annum). UK catalytic science currently has a strong presence, but there is intense competition in both academic and industrial sectors, and a need for UK industrial activity to shift towards new innovative areas posing major challenges for the future. In light of these challenges the Centre for Catalytic Science endeavours to become a leading institution, both nationally and internationally, in the field and acts to coordinate, promote and advance the UK catalysis research portfolio. The Centre is located on the RAL campus which will allow us both to work closely with the central facilities, to whose development the project will also contribute, and to interact with and contribute to the broader scientific community. The major developments in the in situ characterisation of catalytic materials that have taken place in the recent years have been of immense importance in addressing the complex scientific problems posed by catalytic science The Centre will therefore in pursuing a wide ranging programme of research in catalytic science, develop state-of-the art in situ facilities that will be used for experiments to be conducted at the Diamond, Synchrotron Radiation, ISIS Neutron Scattering and Central Laser Facilities. Such experiments will allow us to probe the structure and evolution of catalysts at the molecular level during their operation; but their effectiveness will require the on-line studies to be integrated with off line experimentation in the Complex, within which we will establish a broad range of experimental facilities.

The research areas that have been outlined as major themes within the Centre for Catalytic Science are sustainable catalyst technologies for organic transformations, catalysis for alternative fuels, and catalysis in the protection of the environment. The Centre for Catalytic Science will set-up collaborative research programmes to tackle these major themes and exploit the unrivalled collective expertise the consortium has in catalyst design, testing and characterisation. Moreover, the Centre will be able to make substantial advances by working closely with scientists from ISIS and Diamond to effectively utilise the world-leading facilities present on the RAL campus.

Planned Impact

The proposed research is aimed at gaining new knowledge of how catalysts function at the molecular level. As such, it will be of major benefit to the UK and international groups in catalytic science and in cognate fields in materials and bioscience. The relevance and impact on industrial research will also be substantial , and by maintaining the strength of UK catalytic science it will make a broader underpinning contribution to the UK economy. By contributing to facility development the project will also benefit a wide user community. The work will be disseminated by standard academic routes - publication in journals of the highest quality (in which the applicants have an excellent track record) and at conferences. Additionally we will make appropriate use of the media and web to publicise the new science. The applicants have strong and wide networks of collaboration, assisting effective dissemination, which will be further enhanced by the proposed visitors programme and through an annual workshop on catalytic science at the Centre. More generally, we aim to make the Centre a major hub for catalytic science on the world stage.

The equipment detailed in this proposal will see significant benefits in the near term, with all items in effective operation by the start of the forthcoming academic year. These items will significantly aid the discovery of novel catalyst materials, which will have industrially relevant applications in the fields of sustainable organic transformations, energy generation, and environmental protection.

Societal impact will follow from advances enabled by the research in sustainable manufacturing leading to greener and cleaner processes and products with reduced environmental impact. Contributions will also be made to the provision of sustainable energy and reductions in energy demands of manufacturing sectors. Additional societal impact will follow from the role of the fundamental research undertaken by the Centre in assisting the development of advanced routes to new pharmaceutical products.

The UK economy will benefit from the role of the Centre in assisting innovation in catalysis manufacture. The large and successful chemical sector, including over 3200 companies and a dynamic SME component, faces intense international competition. The collaborations and interactions both within the Centre and between the Centre and Industry will promote economic impact, which will extend beyond the chemical sector to industries that rely on advances in materials and processes, including automotive, aerospace and electronics sectors.

Knowledge exchange will be vigorously promoted by the Centre through greater integration between the participating research groups and their extensive networks of collaborations and with scientists and facilities on the Harwell/RAL campus. This exchange will lead to scientific advances not only in the development of state-of-the-art equipment but also in sustainable chemical processes. The people benefits and impact will be substantial by the provision of trained research workers whose skills will be necessary for R&D programmes required for market innovation to occur.The management and dissemination plans are designed to maximise impact. The Management Board at the Centre will monitor and advise on impact and the annual dissemination conference will be aimed at the key beneficiaries. The collaborating team have wide ranging experience in the dissemination of their science and the promotion of its impact.

Publications

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Aponte JC (2019) Analyses of Aliphatic Aldehydes and Ketones in Carbonaceous Chondrites. in ACS earth & space chemistry

 
Description We have developed new research facilities at UCL in the area of nanotechnology and robotics as well as new experiments commissioned at Diamond Light Source for users across the UK Catalysis Hub, the first of this kind in the UK.

Under the piece of equipment Video Liquid Transmission Electron Microscopy, we have;

• Established a UK facility for liquid phase TEM imaging to provide much needed capacity building across a range of applications involving soft matter, biomaterials, biological physics, synthetic biology, and nanomaterials design;
• Pioneered new imaging techniques exploiting the unique liquid nature of the samples to establish Brownian 3D tomography techniques;
• Established high content correlative microscopy with automated chemical and physical analysis.
• Established the Liquid TEM facilities at UCL as a leading and pioneer facility for protein 3D reconstruction from Liquid TEM imaging in the emerging field of Liquid TEM imaging.
• Implemented novel deep learning-based computational methods for processing Liquid TEM data.

Under the piece of equipment MilliKelvin Experiments Utilising Vector Magnetic Field, we have found that electrons, which are responsible for electricity, can, in solids, under certain circumstances behave as if their electrical charge was reduced from the normal value and took particular fractions of this normal value. In the past this was only achieved by the use of an intense magnetic field but we have discovered a new situation where different physics caused it to appear in the absence of a magnetic field.

Under the piece of equipment Carl Zeiss Orion "Nanofab" Neon Focussed Ion-Beam, we have found that Neon FIB can be used to fabricate superconducting nanowires for applications in quantum technologies. The nanowires can be incorporated into superconducting microwave resonators (for qubit state readout, for example) without compromising the quality factor.

Under the piece of equipment "A 700 MHz broadband cryoprobe and NMR spectrometer at UCL Chemistry", it could be highlighted;

Many research groups from UCL, as well as other UK academic and industrial organisations, have made use of the multinuclear 700 MHz NMR facility at UCL/Chemistry since its installation in July 2017. The most significant achievement of the award is that our researchers from UCL and outside are provided with easy and immediate access to the multinuclear 700 MHz NMR facility with a broadband cryoprobe. Access to such a spectrometer with diverse capabilities facilitates and enhances the structural research by our users. Successful applications include multinuclear 1H, 11B, 13C, 15N, 19F, 29Si, 31P and 119Sn NMR measurements. As a recent example, we have shown that an unambiguous structure assignment of regioisomers of "clickable" pyridazinediones, used as reversible covalent cysteine modifiers, could be made via the 15N NMR assignments followed by 1H and 13C NMR analysis (DOI: 10.1039/d3sc04976k). The need for 15N NMR was dictated by the specific structure of molecules involved. This type of NMR measurements were possible only due to the high sensitivity provided by the 700 MHz facility with a multinuclear cryoprobe.

In the area of medicinal chemistry, the new chemicals described by Prof David Selwood (UCL) block one of the cancer-hiding mechanisms and reveal the tumour to the immune system. This establishes a new way to treat tumours. The key finding is that the immune response of regulatory T-cells can be affected by a small molecule antagonist of the neuropilin-1 protein. The discovery of this antagonist (EG01377) was published in Journal of Medicinal Chemistry (DOI 10.1021/acs.jmedchem.8b00210). Further work in this area has established a role for pain transmission for the VEGF-neuropilin-1 signalling axis. In a collaboration with University of Florida, Prof Selwood has shown that blockade of neuropilin-1 with a novel antagonist EG01449, characterised by 700 MHz NMR, blocks pain. Researchers from Alzheimer's Research UK UCL Drug Discovery Institute have reported a new efficient chiral synthesis of enantiopure arimoclomol, which has progressed to human clinical studies for evaluation as a potential treatment for SOD1 (superoxide dismutase 1 gene) positive familial amyotrophic lateral sclerosis (ALS). One other major finding led to the development of compound ARUK3001185 which is being evaluated in animal models of Alzheimer's Disease with an eye to future clinical trials. From the use of the facility by industrial companies, verification of the identity of herbicide and insecticide compounds on the 700 MHz NMR was carried out on a confidential basis. Nearly 1000 NMR spectra for Abcam Plc (Cambridge) between November 2017 and November 2022 for the characterisation of chemicals prepared by them. The 19F NMR capability of the facility was used by researchers from Key Organics.

Below we list some of the research subject areas and findings, which were received in response to our request to contribute to this report:

Prof Matthew Powner (Department of Chemistry, UCL, co-applicant in the EPSRC application for the multinuclear 700 MHz NMR facility):

1. We have discovered a chemoselective peptide ligation in water (see Canavelli et al. Nature, 2019). By exploiting amino nitriles we have discovered a highly robust mechanism to access thioacids, thioester and their facile and selective coupling to a-aminonitriles in water. Two essential features enable peptide ligation in water: the reactivity and pKaH of a-aminonitriles make them compatible with ligation at neutral pH and N-acylation stabilizes the peptide product and activates the peptide precursor to (biomimetic) N-to-C peptide ligation. The unique reactivity of a-aminonitriles provides a direct link between canonical peptide structures of biology and prebiotic synthesis. All amino acids and their derivatives were coupled in good-to-excellent yields. We observed unprecedented protecting-group-free ligation for all 20 proteinogenic side-chain residues-including His, Asp, Lys, Cys, Ser, Thr and Tyr, which are all essential to enzyme catalysis but notoriously difficult to ligate under previously reported prebiotic conditions. Interestingly, although we observed poor selectivity for a-coupling of amino acid lysine (1.2:1 a/e) and amino acid amide lysinamide (2.7:1 a/e), lysine nitrile ligated with exceptional a-selectivity (>80:1 a/e). The intermolecular coupling of aminonitriles is also observed to outcompete lysine thioacid lactamization across a broad pH range to give Ac-a-Lys-Gly-CN. The chemoselective coupling of lysine residues at both the C and N termini of peptides underscores that aminonitrile ligation is not only prebiotically plausible, but that it is also predisposed to yield a-peptides.

2. We have developed the first prebiotic synthesis of proteinogenic amino acid cysteine, via a novel nitrile-mediated biomimetic reaction pathway (see Foden et al. Science, 2020). Aminonitriles are generally readily produced by Strecker reactions, but the origin of cysteine-the thiol-bearing amino acid-was not understood. The aminothiol moiety of cysteine is chemically incompatible with nitriles at physiological pH, and it is widely believed that cysteine was a biological invention and a late addition to the genetic code. The importance of cysteine (and its derivatives, such as co-enzyme A) is directly at odds with the prevailing hypothesis which assumes its absence at the origin of life. Cysteine is the primary organic source of sulfide in biology. It is also an important residue within enzyme active sites, with key functions in catalysis and electron transfer, as well as being essential in iron-sulfur proteins and forming inter- and intrapeptide crosslinks. It, therefore, seems almost inconceivable that cysteinyl thiols were not present during the development of nascent biology, and yet this is not the prevailing view. We have now shown that cysteine is a product of simple prebiotic chemistry. This chemistry had remained undiscovered, because the origins of life researchers have focused on amino acid synthesis and ligation, rather than aminonitrile chemistry. Our discovery supports the hypothesis that cysteine was simply a secondary product of serine chemistry at the origins of life (as it is today in biology - as a part of 'the serine family' of amino acids).

3. We have discovered a novel protecting group free, activating agent-free catalytic peptide ligation strategy that operates in neutral water (see Foden et al. published in Science, 2020). Thiol-catalysed peptide ligations are remarkably specific and selective to proteinogenic peptide synthesis. For example, the reaction of Ac-Gly-CN and Ac-ß-Ala-CN (1:1; 200 mM) with Gly (200 mM) and Ac-Cys-OH (30 mol%) results in exclusive a-amidonitrile coupling to furnish Ac-GlyN-Gly-OH (65%) with no detectable beta-coupling of Ac-ß-Ala-CN. We also observed only a-ligation upon challenging our catalytic ligation with N-acetylglutamine dinitrile. Finally, we only observed coupling of proteinogenic Ala in competition with a,a-disubstituted (non-proteinogenic amino acid) Aib. The observed selectivity may have been a key element in the emergence of proteinogenic a-peptides in extant biology. Thiol-catalysed coupling of a-amidonitriles with a-amino acids is highly general; all proteinogenic a-amino acids coupled with Ac-Gly-CN to give peptidyl amidines in good yields at pH 7. However, we observed that dipeptides derived from Ser, Thr and Asn underwent pronounced amidine hydrolysis (at pH 7) to the corresponding peptides. In the reactions of Ser and Thr, we observed oxazoline intermediates, suggesting that intramolecular catalysis by the amino acid side chain was responsible for rapid amidine hydrolysis. Having observed that the peptidyl amidine derived from Asn hydrolysed, we envisaged that amino amides (and therefore peptides) would behave similarly. We next demonstrated amides intramolecularly catalysed amidine hydrolysis by coupling the proteinogenic amino amides, resulting in selective dipeptide synthesis, irrespective of their side chain. Therefore, thiol-catalysis can be used to streamline (prebiotic) peptide fragment ligations, side-stepping the stoichiometric formation of thioacids and instead directly couple peptide-nitrile fragments. To test this novel catalytic-fragment ligation we coupled glycyl peptide nitriles with various peptides and observed excellent yields of peptides. It is remarkable that a single amino acid residue, cysteine, provides robust catalysis for peptide ligation in water and their inherent catalytic activity makes simple cysteinyl peptides an excellent starting point from which to evolve more complex enzymes and protometabolic reactions in an abiotic environment. Our data support a scenario in which nitriles served as an early energy currency on the primordial Earth, perhaps acting as a forerunner to ATP and thioesters that drive reactions in extant biology.

4. We have demonstrated diamidophosphate can be harnessed to achieve Strecker amino acid synthesis. The high yield of N-phosphoro-aminonitriles and their selective transformations provides new insights into prebiotic amino acid synthesis and activation.

5. We have developed a new method to achieve a divergent synthesis of purine and pyrimidine nucleotide for a common precursor (Roberts et al Nat. Commun 2018). The generational simplicity of accessing arabino-nucleosides suggests that ANA may have played a key role in primordial nucleic acids prior to or during the emergence of RNA. We collaborated with Dimitar Sasselov (Harvard Astronomy) and Rafal Szabla (Edinburgh Chemistry) to understand the mechanism of our novel purine photo-reduction and uncovered the chemical mechanism that favours the reduction of canonical nucleosides A and G, but the photochemical destruction of non-canonical inosine (I). Photochemical selection is observed in both ribo- and arabino-stereochemistries and provides a chemical selection for the canonical nucleosides over non-canonical inosine.

6. We have developed methods for the photochemical selection of nucleotide stereochemistry, which lead to a novel synthesis of Watson-Crick base pairing TNA nucleoside that are punitive evolutionary precursors to RNA. (See Colville and Powner, Angewandte Chemie 2021).

7. We have developed a new prebiotic strategy to access nucleotide 5'-phosphates in water. The new strategy opens new pathways to explore nucleotide syntheses and activations, which are closely aligned with the biochemical strategies exploited by extant life. We have now developed this work further to realise acetylation-controlled nucleotide photoanomerisation.

8. We have demonstrated that N-phospho-aminonitriles can not only be highly efficiently synthesised in neutral water but the neutral phosphorostrecker reaction provides excellent selectivity for a proteinogenic amino acid over non-natural a,a-disubstituted amino nitrile (see Ashe et al in Nature - Communications Chemistry, 2019).

9. We have developed new chiral aldehydes for analysis and as standards to use for investigating the chemical composition of meteorite samples in collaboration with scientists at the Solar System Exploration Division, NASA Goddard Space Flight Center, USA (see Aponte et al in ACS Earth Space and Chemistry, 2019). Access to UCL high-field NMR has been fundamental to all our advances.

Prof David Selwood (Wolfson Institute for Biomedical Research, UCL):

1. Cancers hide (cloak) themselves from immune system attack by several means. The new chemicals described by us block one of these cloaking mechanisms and reveal the tumour to the immune system. This establishes a new way to treat tumours. The key finding is that the immune response of regulatory T-cells can be affected by a small molecule antagonist of the neuropilin-1 protein. The discovery of this antagonist (EG01377) is described in our paper titled "Small Molecule Neuropilin-1 Antagonists Combine Antiangiogenic and Antitumor Activity with Immune Modulation through Reduction of Transforming Growth Factor Beta (TGFß) Production in Regulatory T-Cells". Further work in this area has established a role for pain transmission for the VEGF- neuropilin-1 signalling axis. With our collaborator Rajesh Khanna (University of Florida) we have shown that blockade of neuropilin-1 with a novel antagonist EG01449, designed by us and characterised by 700 MHz NMR, blocks pain (manuscript in preparation for Journal of Medicinal Chemistry).

2. Inhibitors of lentiviral innate defence mechanisms in human stems cells were discovered. Transiently blocking these defences greatly enhances the efficiency of gene transfer into stem cells. This work will have a major impact on gene therapy for rare bloodborne diseases. The 700MHz NMR offers precise and high-definition assessment of the structures of the complex natural products such as depsipeptides which are used for these new therapies. Two publications are in preparation and the IP on the molecules is protected by a patent filed by UCL business PCT: WO2023247937A1.

3. PROTACs (proteolysis targeting chimeras) with potential as new antiviral therapies were discovered. These molecules are organic chemistry constructs with bivalent protein binding activity allowing selective chemical knockdown of host intracellular proteins. Part of this work was published in eLife in 2020. New PROTACs based on the depsi-peptide framework have now been designed and show unprecedented selectivity for a particular cyclophilin isoform. This work appears in an ACS abstract 3739968 and was presented at the ACS fall meeting 2022 "Macrocyclic PROTACs as selective cyclophilin degraders and potent HIV inhibitors" Date: August 22, 2022. This work is in review at Nature Communications.

Dr Hien Nguyen (City University): We have developed a range of novel low-cost, portable and selective fibre optic chemical sensors for the detection of drugs and heavy metals. The use of the NMR facility at UCL is essential in the organic synthesis stage where various novel fluorescent receptors have been developed and used as the sensing materials for the sensors. Two papers have been published in 2019/20, titled "Novel coumarin-based pH-sensitive fluorescent probes for the highly alkaline pH region" and "A Turn-On Fluorescence-Based Fibre Optic Sensor for the Detection of Mercury". Dr Vijay Chudasama (Department of Chemistry, UCL): The use of the UCL 700MHz NMR facility was paramount in helping us elucidate the structure of two different tautomers of a medicinally important heterocycle - indazole. This was the key finding during the development of synthesis for both indazole tautomers through the use of a single branch point intermediate. We were able to develop the efficient formation of 1H- and 2H- indazoles from a single branch point intermediate. The UCL 700MHz NMR facility was also used to characterise the structure of all the analogues formed through this method.

Drs Hannah Woodward, Ben Atkinson, David Steadman, Paul Fish, Matt Cheeseman and Robert Lesniak (Alzheimer's Research UK UCL Drug Discovery Institute): We regularly use the 700 MHz and other NMR instruments at UCL Chemistry to obtain high-resolution NMR spectra. This allows us to fully characterise all of the small molecules we synthesise in our research projects, which are aimed at finding modulators of targets implicated in the progression of Alzheimer's or other neurodegenerative diseases. As an example, a new efficient chiral synthesis of enantiopure arimoclomol was reported recently. This arimoclomol has progressed to human clinical studies for evaluation as a potential treatment for SOD1 (superoxide dismutase 1 gene) positive familial amyotrophic lateral sclerosis (ALS). Off-target pharmacology was evaluated against a representative set of drug targets and showed modest binding to a few kinases. Pharmacokinetic data were generated in vivo in mice and showed a low brain : plasma ratio. The reported pharmacology and pharmacokinetic studies will be helpful in gaining a better understanding of the pharmacokinetic-pharmacodynamic relationship of arimoclomol in disease models. Overall, our research projects are aimed at finding small molecule modulators of targets implicated in the progression of Alzheimer's or other neurodegenerative diseases. We have submitted a patent application which has compounds that were characterised on the 700 as well as a research paper which was published MedChemComm in 2023. Tool compounds for use in neurodegenerative research and compounds for use as inhibitors of key targets for the treatment of neurodegenerative diseases were discovered recently. For our publications and patents, the collaborations were fundamental to the success of the research. Most of the publications resulted from a collaboration between the Oxford and Cambridge ARUK drug discovery institutes and the Wellcome Centre for Human Genetics at the University of Oxford. Additionally, the quality of the emerging molecules from the UCL Drug Discovery Institute (DDI), including those discussed above, is having a great impact on the reputation of the DDI in the scientific community and attracting potential collaborators to approach us as a partner of choice. We plan to progress our research through the drug discovery process and are exploring third-party licensing opportunities. One of the major key findings was from the Notum research project, enabling the development of compound ARUK3001185 which is being evaluated in animal models of Alzheimer's Disease with an eye to future clinical trials. This project used the NMR facilities for the characterisation of small molecules.

Dr Salvador Tomas (Department of Biological Sciences, Birkbeck College): By allowing the careful characterization of the relevant molecular tools and the analysis of self-assembly, data gathered using the UCL NMR facility has enabled us to (i) develop a mathematical model of cooperative assembly in supramolecular polymers; (ii) carry out the detailed study of chemical reactivity in lipid vesicles, and (iii) develop a mathematical model of membrane adhesion. The UCL NMR facility helped us to characterise the cooperativity in self-assembly described in our publication.

Prof Erik Arstad, Dr Thibault Gendon and Dr Michael Porter (Institute of Nuclear Medicine, UCL and Department of Chemistry, UCL): The 700 MHz NMR facility together with other NMRs at UCL Chemistry is used in our research daily as part of our research on aromatic radiofluorination. In addition to routine analysis, the NMR spectrometers were used to elucidate reaction mechanisms and predict the outcome of the radiofluorination reactions. In particular, the 700 MHz NMR was used to confirm the structure of complex molecules, which otherwise is difficult to analyse with the other instruments. We have shown that the efficiency of aromatic radiofluorination using dibenzothiophene sulfonium salts is correlated with the 19F NMR chemical shift of the non-radioactive fluorinated reference. Recently, we have reported a novel intramolecular ring-closing reaction of biaryl thioethers that gives access to highly functionalized dibenzothiophene sulfonium salts under mild conditions. The resulting precursors react regioselectively with fluoroarenes in predictable radiochemical yields. The strategy expands the available radiochemical space and provides superior labelling efficiency for clinically relevant Positron Emission Tomography (PET) tracers.

Dr Michael Porter (Department of Chemistry, UCL): We have developed a novel organic transformation. The 700 MHz NMR has been valuable in identifying and quantifying the products from (i) a novel electrochemical trifluoromethylation and (ii) a novel oxidative cyclisation of homopropargylic sulfonamides.

Prof Claire Carmalt and Dr Caroline Knapp (Department of Chemistry, UCL): Our NMR studies, including variable-temperature measurements, have focused on gallium alkoxides (please see our recently published paper titled "Structural and Dynamic Properties of Gallium Alkoxides", DOI: 10.1021/acs.inorgchem.9b01496). These are useful as precursors to gallium oxide, which in turn is used in the formation of amorphous oxide semiconductors employed in thin-film photovoltaic devices, as well as in the development of processes towards sustainable high-quality transparent conducting oxide (TCO) films and gas sensing materials. The NMR spectra of chloro gallium bis(alkoxides) were found to vary with the nature of the ligand and the temperature and allowed to establish the dynamics of the molecules studied.

Prof Helen Hailes (Department of Chemistry, UCL):

1. For the publication "Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass", the facility was invaluable in characterizing the products generated from biomass-derived starting materials. Selective dehydration of pentose sugars was achieved under basic or acidic conditions, and the equipment allowed NMR reaction monitoring and the ability to distinguish between the isomeric products formed. Fragments for medicinal chemistry applications containing primary alcohol, ketone, carboxylic acid or amine functional groups were generated, suitable for incorporation into fragment/lead libraries. Funding EPSRC (EP/K503745/1) and building upon outputs from EP/K014897.

2. For the publication 'A Biomimetic Phosphate Catalyzed Pictet-Spengler Reaction for the Synthesis of 1,1'-Disubstituted and Spiro-Tetrahydroisoquinoline Alkaloids', the facility was invaluable for reaction monitoring as the products are readily oxidized, hygroscopic and difficult to purify. In this work, a range of novel 1,1'-disubstituted and spiro-tetrahydroisoquinoline alkaloids were readily prepared in one step and good yields, via this atom-efficient, sustainable synthetic route. Funding BBRSC (BB/N01877X/1).

3. For the publication 'Ene-reductases from a drain metagenome for the selective bioreduction of bicyclic enones', the facility was essential to determine the stereochemistry of ene-reductase enzyme products. In this work, a sequence-based functional metagenomics strategy was used to identify novel ene-reductase enzymes from a drain metagenome. Several new ene-reductases were discovered and effectively applied in the stereoselective bioreduction of bicyclic Wieland-Miescher and Hajos-Parish ketones. Notably, this is the first time such bulky substrates have been successfully transformed with wild-type ene-reductases and the enzymes also showed remarkable organic solvent robustness which is ideal for industrial applications. Funding BBRSC BB/N01877X/1 & BB/L007444/1.

4. For the publication 'Acceptance and Kinetic Resolution of Alpha-Methyl-Substituted Aldehydes by Norcoclaurine Synthases', we have reported the unusual acceptance of alpha-substituted aldehydes, by wild-type Thalictrum flavum Norcoclaurine Synthases to give tetrahydroisoquinoline products. Moreover, the kinetic resolution of several alpha-substituted aldehydes to give tetrahydroisoquinolines with two defined chiral centres in a single step with high conversions was achieved. Active site mutants of Thalictrum flavum Norcoclaurine Synthases were then used which demonstrated the potential to enhance the stereoselectivities in the reaction and improve yields. Funding BBRSC (BB/N01877X/1).

5. For the publication 'Identification and catalytic properties of new epoxide hydrolases from the genomic data of soil bacteria', the facility was invaluable in characterizing the products generated by the epoxide hydrolases identified. New epoxide hydrolases for use in synthesis were discovered and their stereoselectivities were studied. Funding Wellcome Trust . Collaboration: J. Ward, Biochem Eng UCL.

6. For the publication 'Carprofen elicits pleiotropic mechanisms of bactericidal action with the potential to reverse antimicrobial drug resistance in tuberculosis', the facility was invaluable for product characterisation. In this work, Carprofen was found to be a bactericidal drug that inhibited mycobacterial drug efflux mechanisms. It also restricted mycobacterial biofilm growth. Transcriptome profiling revealed that carprofen likely acts by targeting respiration through the disruption of membrane potential. The pleiotropic nature of carprofen's anti-TB action may explain why spontaneous drug-resistant mutants could not be isolated in practice and this immunomodulatory drug and its chemical analogues have the potential to reverse TB antimicrobial drug resistance, offering a swift path to clinical trials of novel TB drug combinations. In summary. new anti-mycobacterial drugs were discovered and studied. Funding the Wellcome Trust (grant code: 108877/Z/15/Z), the BSAC (grant code: bsac-2019-0030) and PreDiCT-TB consortium (http://www.predict-tb.eu) funded by the Innovative Medicines Initiative Joint Undertaking (http://www.imi.europa.eu; grant agreement number: 115337), resources of which were composed of financial contribution from the European Union's Seventh Framework Programme (grant code: FP7/2007-2013) and EFPIA companies' in-kind contribution. Collaboration: S. Bhakta, Birkbeck College, London.

7. For the publication 'Single step syntheses of (1S)-aryl-tetrahydroisoquinolines by norcoclaurine synthases', the facility was essential for product characterisation. In this work, benzaldehydes were explored as substrates and found to be accepted by both wild-type and mutant constructs of norcoclaurine synthase (NCS). In particular, the variant M97V gave a range of (1S)-aryl-THIQs in high yields (48-99%) and e.e.s (79-95%). A co-crystallised structure of the M97V variant with an active site reaction intermediate analogue was also obtained with the ligand in a pre-cyclisation conformation, consistent with (1S)-THIQs formation. Selected THIQs were then used with catechol O-methyltransferases with exceptional regioselectivity. This work demonstrated valuable biocatalytic approaches to a range of (1S)-THIQs. Funding BBRSC; BB/N01877X/1 for D.M.-S. and BB/R021643/1 and 17-ERACoBioTech for F.S. and Wellcome Trust (096626/Z/11/Z) for B.R.L. Collaboration: J. Ward in Biochem Eng UCL, Nick Keep in Birkbeck, Jenny Andexer at the University of Freiburg and Michael Richter at the Fraunhofer Institute.

8. For the publication 'Norcoclaurine Synthase Mediated Stereoselective Synthesis of 1,1'-Disubstituted, Spiro- and Bis-Tetrahydroisoquinoline Alkaloids', we discovered that wild-type NCS and selected variants can be used with aliphatic, cyclic, a-substituted cyclic, heterocyclic, and bicyclic ketones to access challenging non-natural tetrahydroisoquinoline alkaloids (THIAs). We found that fused bicyclic ketones as well as diketones could also be accepted by some of the NCS variants, and in silico modelling was used to provide insights into the rationale for this. Funding BBRSC (BB/N01877X/1) a UCL Dean's Prize and UCL-China Scholarship Council Joint Research Scholarship to J. Z., and a Birkbeck Anniversary PhD scholarship to R.R as part of the London Interdisciplinary Doctoral Program. Collaboration: Dr N. Keep Birkbeck College, J. Ward Biochem Eng, UCL.

9. For the publication 'Mechanoenzymatic reactions with whole cell transaminases: shaken, not stirred', we described the use of mechanoenzymatic approaches with transaminase enzymes. To date, very few mechanoenzymatic reactions have been described. For the first time, transaminases, widely used for the amination of aldehydes and ketones, were employed under mechanoenzymatic conditions to produce amines using significantly less aqueous medium than conventional biocatalytic reactions. The direct use of whole cells was also possible and shorter reaction times could be used to provide amines efficiently with high yields and stereoselectivities.

10. For the publication 'Enzymatic synthesis of benzylisoquinoline alkaloids using a parallel cascade strategy and tyrosinase variants', we described the use of a tyrosinase, tyrosine decarboxylase, transaminase, and norcoclaurine synthase in a parallel cascade design, in order to generate halogenated benzylisoquinoline alkaloids in high enantiomeric excess. Notably, mutagenesis studies were applied to generate tyrosinase mutants, which enhanced the acceptance of halogenated tyrosines for use in the biocatalytic cascades developed.

11. For the publication 'The Discovery of Imine Reductases and their Utilisation for the Synthesis of Tetrahydroisoquinolines', 29 novel imine reductases (IREDs) were revealed through genome mining. Imine reductase activities were screened and some IREDs showed good activities. IREDs with Asn and Glu at the key 187 residue showed a preference for NADH. IREDs were also screened against a series of dihydroisoquinolines to synthesise tetrahydroisoquinolines (THIQs), bioactive alkaloids with a wide range of therapeutic properties. Selected IREDs showed high stereoselectivity, as well as high THIQ yields (>90%) when coupled to a glucose-6-phosphate dehydrogenase for NADPH cofactor recycling.

12. For the publication 'The use of tyrosinases in a chemoenzymatic cascade as a peptide ligation strategy', a new N-terminal tyrosine-containing peptide ligation method with aldehydes, utilising a Pictet-Spengler reaction was explored. In a key step, tyrosinase enzymes were used to convert L-tyrosine to L-3,4-dihydroxyphenyl alanine (L-DOPA) residues, generating suitable functionality for the Pictet-Spengler coupling. This new chemoenzymatic coupling strategy can be used for fluorescent tagging and peptide ligation purposes.

13. Publication 'C-1 Substituted isoquinolines potentiate the antimycobacterial activity of rifampicin and ethambutol' DOI 10.3389/frabi.2023.1095013: Mycobacterium tuberculosis remains one of the leading infectious causes of death worldwide. The development of novel antimycobacterial compounds is essential to reinforce the existing antitubercular drug discovery pipeline. Previous work established that several C-1 substituted tetrahydroisoquinolines have antimycobacterial activity and three chemical series based on these structures were synthesised and assayed for their antimycobacterial potency, mammalian cell toxicity, inhibition of whole-cell efflux and synergism with isoniazid, rifampicin, and ethambutol. Potent whole-cell efflux inhibitors and synergistic compounds were identified, suggesting potential development as adjuncts to existing anti-tuberculosis chemotherapy.

14. Publication 'Mechanoenzymatic reactions for the hydrolysis of PET' DOI 10.1039/d3ra01708g: Recent advances in the enzymatic degradation of poly(ethylene terphthalate) (PET) have led to a number of PET hydrolytic enzymes and mutants being developed. We have reported the first use of whole cell PETase enzymes to breakdown a variety of PET materials (including post-consumer samples) using mechanoenzymatic ball milling. Increased yields of PET degradation by whole cell PETase enzymes of up to 27-fold were achieved by utilising ball milling cycles of reactive aging, when compared with typical solution-based reactions. This methodology also gave a 2600-fold decrease in the solvent required when compared with other leading degradation reactions in the field and a 30-fold decrease in comparison to reported industrial scale PET hydrolysis reactions.

15. Publication 'Multi-enzyme catalysed processes using purified and whole-cell biocatalysts towards a 1,3,4-substituted tetrahydroisoquinoline', DOI 10.1039/d3ra01210g: Two multi-enzyme catalysed processes were carried out to access a 1,3,4-substituted tetrahydroisoquinoline (THIQ), using either purified enzymes or lyophilised whole-cell catalysts. A key focus was the first step, in which the reduction of 3-hydroxybenzoic acid into 3-hydroxybenzaldehyde using a carboxylate reductase (CAR) enzyme. Two different recycling approaches, either using purified enzymes or lyophilised whole-cells were established and both of them showed high conversions of the acid into the benzaldehyde (>80%). Subsequent steps were performed in a sequential mode to avoid cross-reactivities and the formation of several side products, leading to the formation of the target THIQ product with high HPLC yields (>90%, ic > 90%). Overall, this led to the formation of a product with three chiral centres via an atom-efficient approach to stereoisomerically pure THIQ.

16. Publication 'The use of tyrosinases in a chemoenzymatic cascade as a peptide ligation strategy', DOI 10.1039/d2cb00237j: A new N-terminal tyrosine-containing peptide ligation method with aldehydes, utilising a Pictet-Spengler reaction was achieved. In a key step, tyrosinase enzymes were used to convert L-tyrosine to L-3,4-dihydroxyphenyl alanine residues, generating suitable functionality for a Pictet-Spengler coupling to aldehyde moitites. This new chemoenzymatic coupling strategy can be used for fluorescent-tagging and peptide ligation purposes.

Prof Tom Sheppard and Dr Helen Allan (Department of Chemistry, UCL):

1. The study of boron-mediated reactions in organic synthesis and reactions of organoboron compounds is greatly facilitated by the use of 11B NMR. However, the identification and characterization of reaction intermediates in often complex systems is far from trivial, as 11B NMR does not provide any detailed structural information. We have shown that greater insight into the structures present in such systems can be obtained by using DFT chemical shift calculations to support or exclude proposed reaction intermediates. We have reported a rapid and accessible approach to the calculation of 11B NMR shifts that is applicable to a wide range of organoboron compounds.

2. We have shown how dihalohydration reactions of propargylic alcohols can be used to access a wide variety of useful halogenated building blocks. A novel procedure for dibromohydration of alkynes has been developed, and a selection of dichloro and dibromo diols and cyclic ethers were synthesized. The dihalohydration of homo-propargylic alcohols provides a useful route to 3-halofurans, which were shown to readily undergo cycloaddition reactions under mild conditions. A novel ring expansion of propargylic alcohols containing a cyclopropylalkyne is shown to provide access to halogenated alkenyl-cyclobutanes.

3. In 2021, we have begun a new EPSRC-funded project on the mechanistic study of boron-catalysed amidation reactions (EP/T030488/1) in collaboration with Professor Andy Whiting (Durham University), Professor Henry Rzepa (Imperial College London), Dr Jordi Burés (University of Manchester) and scientists from GSK, AstraZeneca & Syngenta. This project will make extensive use of the 700 MHz NMR for elucidating the structures of novel catalysts and potential reaction intermediates. Previous work in this area (outlined above in (1)) also led to funding for a 3-year collaborative PDRA with AstraZeneca

4. We have carried out a detailed study of directing group effects in Pd-catalysed C-H activation reactions of aliphatic amines in collaboration with AstraZeneca. This work made extensive use of the 700 MHz NMR for structure determination of often-complex products (publication 10.1002/adsc.202000726). This work led to further funding for a 3-year PDRA collaboration with AstraZeneca.

5. Collaboration with Prof Matt Powner on prebiotic amidation (see Foden et al. Science, 2020, see above).

6. The use of DFT/NMR analysis to confirm the stereochemistry of two deuterated diastereoisomers has allowed us to confirm the proposed reaction mechanism of the ene reductase reduction of fluoroalkenes. This has aided understanding, supporting modelling studies of the active site, and will add impact to our publication. Confirmation that both hydride addition and protonation are stereoselective will also enable us to pursue the research further with more functionalised compounds to produce contiguous stereocentres.

Prof Alethea Tabor (Department of Chemistry, UCL):

1. We have used the 700 MHz NMR machine to continue her studies on the folding and biological activity of the tarantula toxin ProTx-II. This is an inhibitory cystine knot (ICK) peptide that shows highly selective and potent binding to the Nav1.7 ion channel and hence is an important lead for the treatment of chronic pain. In recent work her group have developed methods for preparing analogues of ProTx-II that can be derivatised with biotin or fluorophores, or with photoactivatable groups, to probe the binding of ProTx-II to Nav1.7, and they have used 700 MHz NMR to demonstrate whether the resulting peptides are correctly folded.

2. The 700 MHz NMR machine was also used to develop new techniques to characterise the surface functionalisation of semiconducting polymer nanoparticles (SNP). These SNP are being developed as novel contrast agents for photoacoustic and near-infrared imaging of tumours, which will allow for precision image-guided surgery of cancer patients. We are pioneering the use of surface-modified SNP that have n-ethylene glycol coatings (to prolong circulation in vivo) and peptide epitopes targeted to cell surface receptors, such as EGFR, that are overexpressed on certain cancer cells. Mass spectrometry and TEM techniques cannot give accurate quantitation of whether the surface functionalisation is complete: however, using the 700 MHz NMR we have been able to follow the progress of the reactions and optimise the surface functionalisation. The results have been published (DOI 10.1016/j.bmc.2023.117412).

Dr Gareth Williams and Karolina Dziemidowicz, PhD Candidate (School of Pharmacy, UCL): The 700MHz NMR facility, including its 19F NMR capability, was used in our project titled "Perfluorophenyl azide functionalisation of biodegradable polymers". This project focuses on the surface modification of electrospun polycaprolactone fibres to enable therapeutic protein delivery.

Dr Mukhlesur Rahman (School of Health, Sports and Bioscience, University of East London; Currently in Liverpool John Moores University): Have discovered terpenes with potential antibacterial activity against a series of clinical isolates of multi-drug resistant and methicillin-resistant staphylococcus aureus. The structures of compounds were established using the analysis of one-dimensional and two-dimensional NMR data and mass spectra.

Prof Ipsita Roy and Dr Pooja Bassnet (Department of Life Science, University of Westminster): We have used the 700MHz NMR facility for the research project involving the production of a family of biodegradable polymers such as polyhydroxyalkanoates (PHAs). PHAs are produced by a range of bacterial species using fermentation technology. We use NMR to identify the structure of the PHAs produced. The monomeric composition of PHAs is affected by the type of carbon substrate and the media composition. PHAs are used for a range of medical applications such as medical device development (coronary artery stents, nerve conduits, wound healing patches), tissue engineering scaffolds in Regenerative Medicine and controlled drug delivery.

Fane F. K. Mensah, PhD Candidate, and Prof Geraldine Cambridge (Division of Medicine, Centre of Rheumatology Research, UCL): CD24 expression on pro-B cells plays a role in B cell selection and development in the bone marrow. We previously detected higher CD24 expression and frequency within IgD+ naïve and memory B cells in patients with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) compared with age-matched healthy controls (HC). We have reported the results of our investigations of the relationship between CD24 expression and B cell maturation. The relationship between CD24 expression to cycles of proliferation and metabolism in purified B cells from HC was investigated using the 700MHz NMR facility at UCL Chemistry. Currently, there is a manuscript under preparation in which we describe changes in an additional 26 metabolites using the spectral data obtained on the 700MHz NMR facility at UCL Chemistry. In both studies, we used the 700 MHz NMR to study the metabolic processes that occur during B cell maturation upon in vitro stimulation by measuring the relative levels of different metabolites present in the culture medium. For the first time, we have been able to follow changes in metabolite concentrations as well as changes in B cell phenotypes throughout in vitro B cell culture. This has not been done before and the developed assay can be used to test interventions during culture to follow changes in metabolite consumption and secretion, specific for B cells.

Prof Junwang Tang and Dr Christopher Windle (Department of Chemical Engineering, UCL): We have discovered a new catalyst for the selective oxidation of methane. Two papers have been published: "Covalent grafting of molecular catalysts on C3NxHy as robust, efficient and well-defined photocatalysts for solar fuel synthesis" and "Rational Design of High-Concentration Ti3+ in Porous Carbon-Rich TiOx Nanosheets for Highly-Efficiency Photocatalytic Ammonia Synthesis".

Dr Stefan Guldin (Department of Chemical Engineering, UCL): For the publication "Fractionation of block copolymers for pore size control and reduced dispersity in mesoporous inorganic thin films", our findings are relevant to mesoporous inorganic thin films, which are promising materials for a variety of applications, including sensing, catalysis, protective coatings, energy generation and storage. In many cases, precise control over a bicontinuous porous network on the 10 nm length scale is crucial for their operation. A particularly promising route for structure formation utilizes block copolymer (BCP) micelles in solution. We have shown how chromatographic fractionation of BCPs provides a powerful method to control the pore size and dispersity of the resulting mesoporous thin films. The 700 MHz NMR facility at UCL Chemistry was used for structural studies in this work. Prof Ivan Parkin and Cláudio Lourenco, PhD Candidate (Department of Chemistry, UCL): The aim of our project is to investigate active components of peroxide- and ROS-based antimicrobial systems which promote cleaning and antimicrobial effects (ROS = Reactive Oxygen Species). NMR studies are crucial for the determination of the stoichiometry of chemical reactions under different atmospheric conditions and concentrations. We also aim to develop new analytical methods for investigating how different reactant chemicals interact with components of biofilms and biofouling. Improved, novel chemistries would have a widespread application in a range of disinfectant applications. On a different project, we have already used the 700MHz facility to determine the authenticity of different glue samples.
Prof Ivan Parkin and Georgia Fleet, PhD Candidate (Department of Chemistry, UCL): A new method is being developed for analysing biofilm residues in collaboration with the Eastman Dental Hospital and GSK that uses the 700MHz NMR instrument.

Prof Chris Blackman (Department of Chemistry, UCL): A novel nickel dialkylaminoalkoxide precursor has been developed for chemical vapour deposition (CVD) of nickel oxide. A manuscript based on this work has been published (DOI: 10.1039/D1RA03263A).

Prof Gopinathan Sankar and Junwen Gu, PhD Candidate (Department of Chemistry, UCL): We investigate the mesoporous structure formation from commercial zeolite while maintaining the microporous character within the same crystal. Here the effect of pH (between 9 and 11) induced by the use of mild organic ammonium hydroxides and cetyltrimethylammonium bromide (CTAB) on the formation of mesostructures is of particular interest. The investigation also involves the determination of the effect of the Si/Al ratio of the starting zeolite Y on the mesostructure formation within the same pH range. The work also will investigate the creation of macroporous silicalite material resulting in macropores within silicalite crystals.

Dr Gemma Louise-Davis (Department of Chemistry, UCL). The 700 MHz NMR has been used in the following projects:

1. Preparation of metallasilsesquioxanes as novel precursors for MRI contrast agents. This project involves the development of new precursors for high-signal MRI contrast agents. Utilising traditional inorganic synthetic chemistry techniques, complexes composed of Gd-chelates can be prepared as used in the development of nanostructured contrast agents with significantly higher signal than traditional molecular agents, whilst reducing the risk of metal leakage and dangers associated with this.

2. Development of hybrid organic-inorganic composites for diagnostic MRI contrast agents. Medical imaging agents capable of changing their signal profile in situ in the body could be exploited for non-invasive disease diagnostics, of value to clinical medicine. In this project, thermoresponsive polymer species are being developed which can respond to specific environmental markers. In combination with well-established high signal nanocomposite MRI contrast agents, these can hence provide a new route to contrast agents whose signal can be turned 'on' or 'off' in the presence of disease.

3. Targeted imaging agents using glycan chemistry. Bowel cancer is a highly prevalent disease that is often diagnosed at late stages due to lack of symptoms in the earlier, more treatable stages. As such, a route to early diagnosis of this disease is key to increasing survival rates. Current screening through colonoscopies uses diagnostic technician skills to observe and identify cancerous polyps, which are often difficult to distinguish from healthy polyps present in the bowel. This project aims to use sugar chemistry to develop a tool to assist with colonoscopic evaluations of polyps. Targeting of sugars released by cancerous polyps will be exploited to 'tag' these polyps with a high signal imaging agent which will aid easy diagnosis during colonoscopic examinations.

Dr Simoni Da Ros and Dr Katherine Curran (Bartlett School Env, Energy & Resources, Faculty of the Built Environment, UCL): In the project dealing with historic plastics of cultural heritage significance, it has been discovered that hydrolysis plays an important role in the degradation of cellulose acetate and cellulose nitrate materials, as observed by the reduction in the degree of substitution of reference materials which have been aged thermally. It has also been verified that plasticiser loss and cellulose acetate deacetylation are not independent processes and may impact each other. Such discoveries were only feasible due to the high sensitivity of the 700MHz instrument, which allowed to develop accurate methods for the determination of plasticiser content and degree of substitution. In summary, the analysis involving the UCL 700MHz NMR facility has supported the hypothesis that deacetylation plays an important role in the degradation processes of cellulose acetate historic plastics. Experiments have been carried out to determine the relationship between environmental variables such as storage temperature and relative humidity and the rate of deacetylation. Experiments have also been conducted to study the kinetics of plasticiser loss in different environments and data acquired using the NMR facility have supported the hypothesis that the loss of diethyl phthalate from cellulose acetate may be diffusion controlled. Within the Institute of Sustainable Heritage, the 700MHz instrument has supported two MRes, three 3 PhD and the ERC Starting Grant Complex projects, involving Isabella del Gaudio, Rose King, Mark Kearney, Simoni Da Ros and Argyro Gili. These projects involve collaborations with external UCL partners, such as Tate, Arkema, Getty Conservation Institute, Dow Chemicals Ltd, Museum of London and Lacerta Technology. Further details on the ERC Starting Grant COMPLEX project can be found here: https://www.ucl.ac.uk/bartlett/heritage/research/p rojects/current-projects/complex.

Dr Joel Turner and Prof Gavin Jell (Royal Free Hospital, UCL) used solution 29Si NMR measurements for studies of bone cell interactions with silicate species released from bioactive glasses.

Dr Bob Schroeder and Lewis Cowen, PhD Candidate (Department of Chemistry, UCL):

1. Mechanism of Fluoride Doping of BDOPV Organic Semiconductor. Polymeric and molecular semiconductors based on benzodifurandione-based oligo(p-phenylene vinylene (BDOPV) have been shown to have high electron mobilities. Fluoride anions can be used as n-dopants, i.e. a means of introducing negative charge carriers onto BDOPV molecular semiconductors. The mechanisms by which these charges are introduced and the structure of the doped semiconductor are poorly understood. We use NMR experiments in conjunction with other spectroscopic techniques to probe the structural changes in BDOPV organic semiconductors induced by the introduction of n-doping fluoride anions. Both 1H and 19F NMR titrations of a fluoride anion source with an organic semiconductor have given insight into the mechanism of doping in two different solvents. It was discovered that fluoride anions act as a base to deprotonate water in non-protic solvents and the resultant hydroxyl anions form a complex with the semiconductor. 700 MHz NMR was used to identify strongly hydrogen-bonded phenol-type protons in the 1H NMR. When carried out in the protic solvent chloroform, fluoride anions deprotonate the solvent and doping is quenched.

2. Quaternary Ammonium Moieties as n-Dopants for Organic Semiconductors. The 700 MHz NMR was used as part of a full spectroscopic characterisation of self-doping organic semiconductors. A combination of 1H, 13C and 2D NMR studies has allowed us to begin a structural characterisation of the doped species which has never been attempted before. We have now developed an understanding of what intramolecular reactions may be taking place. The structural data from the 700 MHz NMR combined with device performance data is helping us understand the optimum conditions for and the activation energy of doping.

Dr Jon Wilden (Department of Chemistry, UCL): The work in the Wilden group is focused on two main themes (i) new radical methodology including the development and mechanistic aspects of transition metal-free reactions, and (ii) the development of novel peptidomimetics and biologically active molecules. The 700 MHz NMR was used for structure determinations and characterisations in the following research projects:

1) Kate Peck: Enamine Sulfonamide-Alkyne Cycloaddition Reactions.
2) Mark Radigois: Fundamental Studies on Electron Transfer Reactions (EPSRC PDRA EP/M02220X/1).
3) Theodore Hayes: A Novel Enediyne Synthesis from Alkynyl Sulfonamides via Non- Classical Carbenoids.
4) Yi Luo: Towards Understanding the Synthesis and Reactivity of Alkynyl Sulfonamides.
5) Ana-Miruna Androniciu: Synthesis of alpha-aminosulfonamide peptidomimetics. Recently, the 700MHz NMR was also used in the project titled "Electrochemical Reduction of Aerial O2 for Clean, Green, Allylic and Propargylic C-H Activation Reactions".

Prof Jim Anderson (Department of Chemistry, UCL):

1. For the publication "Investigation of the -hydride shift nitro-Mannich reaction. Lewis acid Gd(OTf)3 catalysed conditions were shown to be more general and the reaction was found to be very sensitive to the stability of the intermediate iminium ion. The 700MHz NMR was used for the structural characterisation of reaction products.

2. For the publication "A Divergent Synthetic Route to the Vallesamidine and Schizozygine Alkaloids: Total Synthesis of (+)-Vallesamidine and (+)-14,15-Dehydrostrempeliopine", total synthesis of some complex natural products has been developed. The 700MHz NMR facility was instrumental in deciphering complex stereochemistry in small quantities of advanced intermediates when we were working out our synthetic route.

3. For the publication "Asymmetric synthesis of piperidines using the nitro-Mannich reaction", a diastereoselective nitro-Mannich reaction was employed to control the stereochemistry of functionalized piperidines containing 3 contiguous stereocentres in the 2-,3- and 4- positions. The high resolution provided by the 700MHz NMR allowed full characterisation of various piperidines.

Prof Jamie Baker (Department of Chemistry, UCL): Albumin-drug conjugates and cysteine-to-lysine transfer antibody fragments were studied. Amongst other things, we have used the 700MHz NMR facility to probe the rates associated with new bioconjugation reactions. We have used these findings to develop reagents for the construction of next-generation protein conjugates, which allow the selective delivery of drugs or detectable moieties for diagnostics to target cells. The 700 MHz NMR was also used in one-pot thiol-amine bioconjugation to maleimides: simultaneous stabilisation and dual functionalisation. In the relevant publication (A. Wall, A. G. Wills, N. Forte, C. Bahou, L. Bonin, K. Nicholls, M. T. Ma, V. Chudasama*, J. R. Baker*, Chem. Sci., 2020, 11, 11455-11460), we have presented the first example of an alternative approach to maleimide-conjugate stabilisation, which also infers dual functionalisation in a one-pot fashion. We have applied this conjugation strategy to peptides and proteins to generate stabilised trifunctional conjugates. Research projects, which have made use of the 700MHz NMR, include: Mikesh Patel, PhD project: The development of nitrile reagents for antibody conjugation Charlie Bishop, PhD project: Investigating new mechanisms for cysteine-to-lysine transfer Yanbo Zhao, PhD project: Expanding the scope of Next Generation Maleimides for Antibody Conjugation Muhammed Haque, PhD project: Investigations into antibody conjugation by cysteine-to-lysine transfer Alina Chrzastek, PhD project: Dual reactivity disulfide bridging reagents for antibody bioconjugation Archie Wall, PhD project: Novel Approaches to Site-Selective Protein Modification Using Next-Generation Maleimides Luigia Salerno, PhD project: Active methylene compounds for homogeneous cysteine bioconjugation Nafsika Forte, PDRA on EPSRC grant: Site-selective antibody modification by cysteine-to-lysine transfer (CLT) Roshni Malde: PhD project: Development and Photophysical Investigations of Maleimide Chromophores for Applications in Photoactive Bioconjugates

Dr Cally Haynes (Department of Chemistry, UCL): The Haynes group has been using the 700MHz machine to acquire characterising data for challenging samples of molecules designed to exhibit switchable or controllable solubility. These samples included organic and metal-organic amphiphilic molecules with a tendency to undergo further self-assembly/ aggregation in solution. It was also used to obtain a full spectral characterisation of newly synthesised metal-organic amphiphiles. The title of the relevant project is 'Anion controlled assembly of metal-organic amphiphiles'. The expected long-term findings of this project will be of interest to diverse chemical research fields including supramolecular chemistry, inorganic materials, soft materials, drug delivery and catalysis.

Dr Stefan Howorka (Department of Chemistry, UCL): Insight into the structure and function of photosensitive chemical probes has been achieved via collaborations within UCL Chemistry (Tracey Clarke, Jon Wilden, Guiseppe Battaglia), within UCL (Stephan Beck, UCL Cancer), Cambridge (Hugo Bronstein, Shankar Balasubramanian). We have uncovered the relationship between BODIPY structure and spectroscopic properties to design fluorophores for bioimaging. We have also gained insight into the solvent-dependent photophysics of a red-shifted, biocompatible coumarin photocage. In addition, we have developed a photo-responsive small-molecule approach for the opto-epigenetic modulation of DNA methylation.

Dr Alistair Miller (Darr House): The analysis carried out on the 700MHz NMR allowed to develop collaboration with University of Exeter, leading to a PhD project titled "Authentication of compounds for screening for insecticidal activity." Dr Will Travis (Gurit UK Ltd, Newport): The NMR spectra recorded on the 700MHz instrument helped develop materials for the composites industry with applications in predominately wind turbine and marine industries. The work is still under development and is likely to reach the market soon. The work has not resulted in academic publications and while patents are under draft they will not include the NMR data.

Dr Abil Aliev (Department of Chemistry, UCL, principal investigator in the EPSRC application for the multinuclear 700 MHz NMR facility):

1. The structure of a new compound, Cp(IPr)Ru(H)2SiH(Ph)Cl (IPr = 1,3-bis(2,6-diisopropylphenyl)-imidazole-2-ylidene ) has been established using 1H, 13C and 29Si NMR chemical shifts and J couplings, as well as the X-ray structural analysis and DFT calculations. (in collaboration with Dr J. Saßmannshausen, The Francis Crick Institute).

2. We have used 300 MHz and 700 MHz NMR instruments to measure 119Sn chemical shift anisotropy (CSA) and have shown that a static powder pattern must be analysed in order to improve the accuracy of the CSA asymmetry measurements. (in collaboration with Dr A. Bartok, Rutherford Appleton Laboratory, and Prof J Yates, Department of Materials, University of Oxford).

3. Through detailed NMR measurements and their analysis, we have compared noncovalent interaction of sulfur and oxygen. It was found that compared to oxygen, the sulfur atom can interact with the almost equal facility over the entire range of pi systems studied. The results are important for understanding noncovalent interactions present in proteins (in collaboration with Prof Motherwell, Department of Chemistry, UCL, and Prof Coles. School of Chemistry, University of Southampton). An invited review was also published in 2019 in Chemistry - A European Journal of Chemistry.

4. Over the recent years we have explored the possibilities provided by 15N NMR for 3D structure elucidations of various organic compounds of biological importance. As shown on readily functionalised "clickable" pyridazinediones, used as reversible covalent cysteine modifiers, an unambiguous structure assignment of regioisomers could be made only via the initial 15N NMR assignments followed by 1H and 13C NMR analysis (DOI: 10.1039/d3sc04976k) due to the specific symmetry of the molecules involved. Currently, we are exploring solution and solid-state 15N NMR spectra for structural analysis of vitamins. This type of NMR measurements were possible only due to the high sensitivity provided by the 700 MHz facility.

In addition to those listed above, the 700 MHz NMR instrument has been used by:

Prof Andrea Sella (Department of Chemistry, UCL, in collaboration with researchers from Department of Physics, UCL)
Prof Charles Marson (Department of Chemistry, UCL)
Prof Giuseppe Battaglia (Department of Chemistry, UCL)
Dr Hugo Bronstein (Department of Chemistry, UCL)
Dr Kreso Bucar (Department of Chemistry, UCL)
Prof Xiao Guo (Department of Chemistry, UCL)
Dr Derek MacMillan (Department of Chemistry, UCL)
Dr Robert Palgrave (Department of Chemistry, UCL)
Prof William Motherwell (Department of Chemistry, UCL)
Dr Tung Chun Lee (Institute for Materials Discovery, UCL)
Prof Jonathan Knowles (Eastman Dental Institute, UCL)
Prof Kishor Gulabivala (Eastman Dental Institute, UCL)
Dr Elaine Allan (Eastman Dental Institute, UCL)
Dr Justin Warne (Division of Infection & Immunity, UCL)
Dr Kerstin Sander (Centre for Radiopharmaceutical Chemistry, UCL)
Dr Rose King (Institute of Sustainable Heritage, UCL)
Dr Stephen Hilton (School of Pharmacy, UCL)
Dr Matthew Todd (School of Pharmacy, UCL)
Dr Philip Lowden (Birkbeck College)
PDRA Dr Islam Saidul (Department of Chemistry, UCL)
PDRA Dr Daniel Whitaker (Department of Chemistry, UCL)
PDRA Dr Christian Fernández-García (Department of Chemistry, UCL)
PDRA Dr Laure Benhamou (Department of Chemistry, UCL)
PDRA Dr Thibault Gendron (Department of Chemistry, UCL)
PDRA Dr Dana Chan (Department of Chemistry, UCL)
PDRA Dr Fabien Thoreau (Department of Chemistry, UCL)
PDRA Dr Fatih Sirindil (Department of Chemistry, UCL)
PDRA Dr Yangwei Deng (Department of Chemistry, UCL)
PDRA Dr Robert James Smith (Wolfson Institute, UCL)
PDRA Dr Ben Graham (Wolfson Institute, UCL)
PDRA Dr Suresh Moorthy (Institute for Materials Discovery, UCL)
PDRA Dr Fahima Idiris (School of Pharmacy, UCL)
PDRA Dr Ben Woods (Birkbeck College)
PhD Candidate Cristina Perez Rivero (University of Westminster)
PhD Candidate Yakub Naheem (Royal Free Hospital, UCL)
PhD Candidates Ankan Biswas and Sara Malferrari (Royal Free Hospital, UCL)
PhD Candidate Zalike Keskin Erdogan (Eastman Dental Institute, UCL)
PhD Candidate Mohammad Aljaber (Eastman Dental Institute, UCL)
PhD Candidate Benjamin Bowles (School of Pharmacy, UCL)
Dr Rachel Platel (Lancaster University)
Dr Andrew Atkinson (Kings College)
Prof Eduardo Humeres (Federal University of Santa Catarina, Brazil)
Dr. Fabiola Sciscione (Royal Free Hospital, UCL)
Prof Craig Butts and PhD Candidate Catherine McIntyre (Bristol University)
PhD Candidate Nazanin Owji (Eastman Dental Institute, UCL)
PhD Candidate Sarene Saw (Eastman Dental Institute, UCL)
Drs Louise-Anne Pilcher and John Wong (Abcam) Dr Will Travis (Gurit UK)
Drs Daniel Dumas and Mrs Lorna Bankole (Key Organics Ltd)
PhD Candidate Prachi Dubey (University of Westminster)
PhD Candidate Lorena Lizarraga (University of Westminster)
PhD Candidate Chivu Alexandru (Royal Free Hospital, UCL)
PhD Candidate Huang He (Chemical Engineering, UCL)
PhD Candidate Holly Siddique (School of Health, Sports and Bioscience, University of East London)
Dr Obeng Melody (Royal Free Hospital, UCL) Dr James Sipthorp (Alzheimer's Research UK UCL Drug Discovery Institute)
Dr Elliott Bayle (Alzheimer's Research UK UCL Drug Discovery Institute)

and many others.

Covid Impact: COVID-19 has significantly reduced the laboratory output of the research groups in 2020/21 reducing the average time each researcher can access the lab and NMR instruments, by approximately 50% due to social distancing constraints in UCL laboratories and the weekly cohort system introduced in June 2020. Following the first lockdown in Mar-May 2020, a new access system to the NMR instruments, including preliminary online booking, was implemented in Jun 2020, where selected users (90 in Mar 2021) from each research group placed samples in sample changers of our NMRs, including the 700MHz instrument, and their group members, including new NMR users, remotely access the spectrometer PCs to submit and queue NMR experiments. Remarkably, having remote access to the NMR instruments has resulted in a significant increase in the number of spectra run by our researchers over the recent months despite the weekly cohort system. In particular, for the period of 1 Nov 2020 - 31 Jan 2021, the number of spectra run on the 700MHz instrument increased by 32% compared to the same period a year ago.

Key findings for the last 2 years period (2022-2024) of equipment items funded through this award with a funding end date >5 years are;

• MilliKelvin Experiments Utilising Vector Magnetic Field

The equipment allows the cooling of semiconductor nanostructures down to temperatures of about 15 milliKelvin at which level the transport of electrons is dominated by quantum effects. It has performed an important role in experiments which are part of the Programme Grant "EP/R029075/1, Non-Ergodic Quantum Manipulation". In order to successfully establish an isolated quantum state which may be susceptible to Many Body Localization it is necessary to remove the electron-phonon coupling and eliminate as far as possible any dependence of electron temperature on the phonon bath.

The decoupling has been investigated in disordered Graphene and the inorganic semiconductor Indium Antimonide with considerable success. It was found that the loss of contact between phonons and electrons gave rise to a Negative Differential Resistance which, in the constant current regime, was due to current filament formation. This mechanism was due to electron heating by the field and consequent excitation out of localized states with a resulting sharp rise in conductance.

Additionally it was found that in this regime current was due to electron-electron enhanced hopping in which an exponential dependence on reciprocal temperature was accompanied by a pre-exponential quantized resistivity. This form of hopping is the only situation in which a quantized resistivity has been observed and indicates that the coupling between individual electrons is stronger than that between electrons and phonons. This experimentation is continuing as the observations may indicate that we are close to the onset of Many Body Localization.

• TEM upgrade to STEM-EDS capability, Rapid scanning FT-IR with combined XAFS/DRIFTS accessory and gas handling system, Autoclave reactors, Multi-tubular reactor, GC-MS

The XAFS/ DRIFTS reactor has proved to be an essential too for catalysis systems contributing to improved analysis of operando and in situ reactions allowing Catalytic reactions to be monitored under realistic conditions. The DRIFTS capability analyses surface species and reactants whilst the XAFS capabilities 9 on The Diamond light source allow the evolution of the catalyst structure to be monitored. This combined technique enhances the understanding of how catalysts work and what reaction mechanism are enabling better understanding and design of Catalysts. This analysis can be combined with other techniques; (i) Using vibrational spectroscopy to explore ethanol dehydration, (ii) Assessing the influence of zeolite choice on methanol dehydration to Dimethyl ether, (iii) Using
XAS/DRIFTS/MS spectroscopy for time-resolved operando study of integrated carbon capture and utilisation process and (iv) Studying Ferrocene-derived Fe-metalated porous organic polymer for the core planarity-triggered detoxification of chemical warfare agents

• Carl Zeiss Orion "Nanofab" Neon Focussed Ion-Beam

The Neon Focussed Ion-Beam enabled controllable tunnelling of single flux quanta mediated by Quantum Phase Slip (QPS) in disordered superconducting loops, highlighting a promising pathway towards realizing low-loss nanowire-based QPS devices.

• A UK Facility for 4-D and Correlative Imaging using X-Ray Nano Computed Tomography

X-ray CT has been established as a significant evolving imaging technique in analysing lithium-ion battery failures, addressing limitations such as high costs and time constraints through improved sample preparation and faster acquisition times, paving the way for broader applications in non-invasive evaluation of thermal and internal short circuit failures in battery materials. Recent advancements include the study of high energy lithium-sulfur batteries, achieving uniform intercalation for next generation Li-ion batteries as well as providing invaluable insights into advanced cathode and electrode materials.
X-ray nano-computed tomography along with complementary techniques to provide spatially resolved insights into the type and extent of degradation, not just for battery failures, but it can also inform the development of more efficient and durable catalysts, crucial for advancing the feasibility and sustainability of hydrogen production in the transition to a hydrogen-based economy. On the other hand, the high resolution imaging of the technique enabled insect mechanosensors biomechanics characterisation , suggesting its effect on their sensitivity.

• Video Liquid Transmission Electron Microscopy

Liquid cell TEM was key in observing morphology, distribution and movement of particles in solvents, including successful characterization of Actin fibrils with a periodicity of 8nm with a live cell. For example, protein aggregation in solution enabling the imaging of key molecular events in the aggregation process of Amyloid Beta peptide aggregation as a precursor to amyloid fibril formation, which is believed to be a key process in many modern diseases of the western world including Alzheimer's.

On the other hand, SimpliPyTEM software was developed to process and perform image analysis on liquid TEM data in real time during experimental runs on the TEM, which has now been made freely available to the community. In addition, the development of correlated light and electron microscopy (CLEM) has been established into the field of liquid TEM, as an extension to the traditional CLEM technique which is used for CryoEM.
Exploitation Route Where appropriate equipment is currently listed on UCL's Research Equipment Catalogue. The relevant equipment managers will keep the equipment information up to date and will look to open access to a wider range of users.

Concerning the piece of equipment "A 700 MHz broadband cryoprobe and NMR spectrometer at UCL Chemistry";

Prof Matthew Powner (Department of Chemistry, UCL, co-applicant in the EPSRC application for the multinuclear 700 MHz NMR facility): Elucidating the chemical origins of life. Investigating the origins of Life on other planets (including Mars and current NASA missions of sample return), exploration of exoplanet atmosphere and astrochemistry and developing green chemical strategies for synthesis and catalysis in water. Overall, our findings are of interest to those involved in researching the chemical origins of life, as well as pharmaceuticals and fine chemicals. Selective peptide ligations can be used more generally and more specifically for developing a model for the origins of life on Earth and the context of prebiotic chemistry on exo-planets.

Prof David Selwood (Wolfson Institute for Biomedical Research, UCL): Our findings described above could be developed into a new modality of anti-tumour treatment. The gene therapy enhancers could be licenced and used by pharma companies worldwide. Our new PROTAC discoveries could be developed as new antiviral therapies by industry.

Dr Hien Nguyen (City University): Through publications and commercialisation.

Dr Vijay Chudasama (Department of Chemistry, UCL): Our work has the potential to be used by medical groups who wish to synthesise analogues of heterocyclic-based bioactive compounds for testing. As the two tautomers are observed to have differing bioactive effects, the synthesis, therefore, gives easy access to a much larger range of potentially useful indazole analogues. We have developed several methodologies for the synthesis of pharmaceutically relevant indazoles, benzodiazepines and small molecule drug conjugate scaffolds. We envisage our findings would be particularly useful to those developing more efficient syntheses for pharmaceutically relevant molecules and therapeutics.

Drs Hannah Woodward, Dr Ben Atkinson and David Steadman (Alzheimer's Research UK UCL Drug Discovery Institute): The reported studies described above will contribute towards a better understanding of the pharmacokinetic and pharmacodynamic properties of an experimental drug. Tool compounds discovered could be used for further study and research to understand neurodegenerative diseases and disorders.

Dr Salvador Tomas (Department of Biological Sciences, Birkbeck College): The use of the mathematical tools developed to build up smart lipid vesicles with a range of applications. Our research results can be used by those involved in the development of responsive nanomaterials and nanoreactors for sensing and drug delivery.

Prof Erik Arstad, Dr Thibault Gendon and Dr Michael Porter (Institute of Nuclear Medicine, UCL and Department of Chemistry, UCL): The radiochemistry we developed is likely to have a significant impact on radiopharmaceutical research and lead to the development of the next generation diagnostic tracers. We are already planning for the translation of one such tracer to human studies. The method we published allows radiochemists to acquire the 19F NMR spectrum of the molecule they wish to radiolabel and quickly determine whether our new radiolabelling methodology is suitable for their target or not. We have developed a new type of leaving group (dibenzothiophene sulfonium salts) for nucleophilic aromatic substitution, and have developed this as a platform for manufacturing diagnostic positron emission tomography (PET) tracers.

Dr Michael Porter (Department of Chemistry, UCL): The reactions we have developed may have more widespread use for the synthesis of biologically active compounds in the pharmaceutical and agrochemical sectors. Our research is relevant to the developments of pharmaceuticals and agrochemicals.

Prof Claire Carmalt and Dr Caroline Knapp (Department of Chemistry, UCL): Understanding the dynamics of gallium alkoxide precursors will be useful to others involved in the development of new oxide semiconductors, transparent conducting oxide (TCOs) films and gas sensing materials.

Prof Helen Hailes (Department of Chemistry, UCL):

1. Both AstraZeneca and GSK have samples of the fragments prepared for use in fragment libraries and will provide feedback on an annual basis.
2. We have 2 collaborators, one academic group and a company who are screening the products.
3. The grant is co-funded by ALMAC group and the company has the enzymes for industrial applications.
4 & 5. New enzyme applications.
6. New anti-TB drug hits.
7 & 8. New tetrahydroisoquinoline synthesis of drug-like molecules.

Prof Tom Sheppard (Department of Chemistry, UCL): The findings described above could be used by others for 11B NMR characterisations of reaction intermediates and products. The methodology developed by us can be employed for the preparation of various classes of organic compounds, including those which are of interest to the pharmaceutical industry.

Prof Alethea Tabor (Department of Chemistry, UCL): The methods developed for the studies of folding and aggregation of peptide toxins and peptide surfactants can be employed by other researchers working in the area of biomedicine and peptide chemistry.

Dr Mukhlesur Rahman (School of Health, Sports and Bioscience, University of East London; Currently in Liverpool John Moores University): Bioassay-guided phytochemical investigation on members of the Zingiberacae family can be further explored for the identification of lead anti-Staphylococcal compounds.

Prof Ipsita Roy and Dr Pooja Bassnet (Department of Life Science, University of Westminster): We use NMR to identify the structure of biodegradable polymers, which are useful for a range of medical applications such as medical device development (coronary artery stents, nerve conduits, wound healing patches), as tissue engineering scaffolds in Regenerative Medicine and controlled drug delivery.

Fane F. K. Mensah, PhD Candidate, and Prof Geraldine Cambridge (Division of Medicine, Centre of Rheumatology Research, UCL): Experiments reported by us have not been done before. The developed assay can be used to test interventions during cell culturing in order to follow changes in metabolite consumption and secretion specific for B cells.

Prof Junwang Tang and Dr Christopher Windle (Department of Chemical Engineering, UCL): Our findings provide significant information for the development of new more efficient methane oxidation catalysts.

Dr Stefan Guldin (Department of Chemical Engineering, UCL): We study material formation on the nanoscale by molecular self-assembly and build functional nano-architectures for a variety of fields ranging from chemical sensing and biomedical diagnostics to photovoltaics and optical coatings. For the publication "Fractionation of block copolymers for pore size control and reduced dispersity in mesoporous inorganic thin films", our findings offer a route to obtain a library of monodisperse block copolymers from a polydisperse feedstock and provide important insights on the direct relationship between macromolecular characteristics and the resulting structure-directed mesopores, in particular, related to dispersity.

Prof Ivan Parkin and Cláudio Lourenco, PhD Candidate (Department of Chemistry, UCL): The work carried out in collaboration with industrial partners is relevant for disinfectant applications.

Dr Simoni Da Ros and Dr Katherine Curran (Bartlett School Env, Energy & Resources, Faculty of the Built Environment, UCL): The 700MHz NMR instrument has been highly valuable for achieving several key findings, as explored in the 2021 publication by Da Ros et al. The main key discoveries relate to the determination of kinetic mechanisms involved in plasticiser loss and deacetylation in cellulose acetate historical artefacts. These have in turn been translated to key findings in conservation strategies involving the management of environmental storage conditions. The instrument was key for the development of methods that allowed for quantifying plasticiser loss and average degree of substitution in the above-mentioned artefacts. The NMR spectroscopy is significantly underused in heritage sciences. Our work is helping to raise awareness of its potential in a new field of NMR applications. The findings are expected to impact the conservation strategies in museums and archives or other organisations involved in the preservation of historic plastics. Moreover, by understanding the mechanism of degradation and its main causes, the research may contribute to the development of recycling technologies, which is very important for the management of global solid plastic waste.

Dr Bob Schroeder and Lewis Cowen, PhD Candidate (Department of Chemistry, UCL): Our research is of interest to those involved in the design and synthesis of functional materials for organic electronic applications. An insight into the relatively unknown mechanisms of n-type doping in organic semiconductors allows others to achieve efficient doping in new materials. The development of stable self-doping organic semiconductors will make device processing using doped materials much easier. Lightweight processable energy harvesting materials specifically in organic thermoelectrics and organic photovoltaics.

Prof Jim Anderson (Department of Chemistry, UCL): The divergent synthetic route developed by us will be used for the synthesis of similar alkaloid targets for the investigation of their biological activity.

Dr Jamie Baker (Department of Chemistry, UCL): Reagents and methods for the construction of protein conjugates, such as the ones we have developed, are widely sought. For example, antibody-drug conjugates represent a rapid class of targeted therapeutics, with 3 approved in the last year. However, the reactions to attach the drugs to antibodies are known to be suboptimal - we anticipate our reactions could have a major contribution to the next generation of such conjugates. The stabilisation-dual modification strategy developed by us is likely to have widespread utility in the bioconjugates field, and also in surrounding areas where maleimide chemistry is also widely used e.g. polymer chemistry, nanoparticles, materials etc. The 700 MHz NMR was crucial to this study, as it was employed in the characterisation of the key reagents and in establishing the rates of the newly discovered reactions.

Dr Cally Haynes (Department of Chemistry, UCL): The expected long-term findings of the project using the 700MHz facility will be of interest to diverse chemical research fields including supramolecular chemistry, inorganic materials, soft materials and catalysis. The novel molecules under investigation could be of interest in drug delivery and discovery since we aim to apply these structures to control the pharmacokinetic and pharmacodynamic properties of therapeutic and diagnostic cargoes.

Dr Stefan Howorka (Department of Chemistry, UCL): Develop new photosensitive chemical tools to advance chemical biology, molecular biology, and biomedicine.

Dr Abil Aliev (Department of Chemistry, UCL, principal investigator in the EPSRC application for the multinuclear 700 MHz NMR facility):
1. The work on Ru-H ··· Si interaction will be of interest to those working in the area of organometallic chemistry, as well as in studies of a noncovalent interaction in general;
2. Others working in the area of solid-state NMR spectroscopy, as well as structural characterisations of solid materials, will benefit from the results published by us using tin NMR;
3. The interest in noncovalent interactions has grown fast over the last two decades and our publication titled "Noncovalent Interactions of pi Systems with Sulfur - The Atomic Chameleon of Molecular Recognition" will benefit those interested in noncovalent interactions of sulfur and oxygen atoms. Dr Abil Aliev was invited to write a review article following this publication (DOI doi.org/10.1002/chem.201900854).
Sectors Aerospace

Defence and Marine

Agriculture

Food and Drink

Chemicals

Communities and Social Services/Policy

Creative Economy

Education

Electronics

Energy

Environment

Healthcare

Manufacturing

including Industrial Biotechology

Culture

Heritage

Museums and Collections

Pharmaceuticals and Medical Biotechnology

URL https://www.ucl.ac.uk/bartlett/heritage/research/projects/current-projects/complex
 
Description The strategic equipment was used to purchase a range of chromatographic analysis equipment (HPLC, GC, GC-MS), reactor testing systems (batch and fixed bed reactors) and a rapid scanning FTIR with in situ sample environment for combined XAFS/DRIFTS studies. The equipment was purchased during 2013, with the science program starting in earnest in 2014. The equipment is beginning to make significant contributions to understanding the properties of catalysts during reaction conditions, with the initial publications in 2015. The portfolio of work the equipment underpins is making a valuable input into the fields of environmental protection (e.g. emission control, deNOx and CH4 combustion), sustainable fuels (e.g. upgrading of bio-glycerol, methanol synthesis), and production of commodity chemicals (e.g. methanol oxidation to formaldehyde). Findings from this award, using the piece of equipment Video Liquid Transmission Electron Microscopy, have contributed to research collaborations with DENSsolutions , the company that supplies In-situ holders for environmental TEM microscopy. We have organised a first workshop where our site was used as a demo site for the new generation liquid-heating-bias holders from DENS. This workshop-demo meeting will be held on an annual basis at our facility and delegates will include research institutes, industry and academics. There are various wide-ranging impacts associated with the research work of the users of the multinuclear 700 MHz NMR facility at UCL/Chemistry. Below we list some of them received from research groups using the spectrometer in response to our request to contribute to this report: Prof David Selwood and co-workers have shown that small molecule neuropilin-1 antagonists combine antiangiogenic and antitumor activity with immune modulation through the reduction of TGFß (transforming growth factor beta) production in regulatory T-Cells (PMID: 29648813). Translational funding was secured for this project. Further non-academic impacts through commercial funding for gene therapy applications are being sought. Prof David Selwood's group was the first to show that a host-directed PROTAC (proteolysis targeting chimera) could have antiviral activity (PMID: 32539931). New PROTACs based on the depsi-peptide framework have now been designed and show unprecedented selectivity for a particular cyclophilin isoform. It has been shown that macrocyclic PROTACs can be used as potent HIV inhibitors. A series of compounds have also been developed with the potential to treat Fragile X disease (PMID: 34196695). Overall, new bioactive compounds discovered by Prof David Selwood and co-workers can be developed by other academic groups or by the pharma industry to produce new medicines. Drs Hannah Woodward, Dr Ben Atkinson, David Steadman, Paul Fish, Matt Cheeseman, Robert Lesniak and others (Alzheimer's Research UK UCL Drug Discovery Institute): A major impact was on the Notum research project, which enabled the development of compound ARUK3001185. Currently, this compound is being evaluated in animal models of Alzheimer's Disease with an eye to future clinical trials. The NMR facility was used to characterise compounds used in this and other projects carried out at UCL ARUK Drug Discovery Institute. Tool compounds discovered are relevant for understanding neurodegenerative diseases and disorders and will be used in the drug discovery process, including the exploration of third-party licensing opportunities. Additionally, the quality of the emerging molecules from UCL Drug Discovery Institute is having a great impact on the reputation of the institute in the scientific community and attracting potential collaborators. The existing collaborations with the Oxford and Cambridge ARUK drug discovery institutes and the Wellcome Centre for Human Genetics at the University of Oxford have already led to many publications. Prof Ivan Parkin (Department of Chemistry, UCL): T): Active components of peroxide- and reactive oxygen species (ROS) have been investigated in antimicrobial systems, which promote cleaning and antimicrobial effects. NMR studies were crucial for the determination of the stoichiometry of chemical reactions under different atmospheric conditions and concentrations. A new method is being developed for analysing biofilm residues in collaboration with the Eastman Dental Hospital and GSK that uses the 700MHz NMR. The research undertaken is expected to be of interest to healthcare professionals. Dr Hien Nguyen (City University): A range of novel low-cost, portable and selective fibre optic chemical sensors for the detection of drugs and heavy metals has been developed. We are working with several companies to commercialize what we have developed with the aim of providing a fast screening solution to yield new information on what is an important aspect of improving the environment. Dr Vijay Chudasama (Department of Chemistry, UCL) "A facile route to 1H- and 2H-indazoles from readily accessible acyl hydrazides by exploiting a novel aryne-based molecular rearrangement.": Potentially could contribute to the research in the area of new drug discovery. Several methodologies were developed for the synthesis of pharmaceutically relevant indazoles, benzodiazepines and small molecule drug conjugate scaffolds. Our findings would be particularly useful to those developing more efficient synthesis for pharmaceutically relevant molecules and therapeutics. Dr Salvador Tomas (Department of Biological Sciences, Birkbeck College): Our findings are relevant in abiogenesis. They contribute to a better understanding of life's origin. Our research will boost the development of programmable drug delivery vehicles. The potential societal impact of such devices is difficult to overstate: they will decisively contribute to drastically reducing (and at the fullest of their development, eliminating) the scourge of cancer and infectious diseases. By developing mathematical tools that describe and allow us to predict the behaviour of smart nano-vesicles, our research is contributing to the development of artificial protocells, the building blocks of soft-matter based robots inspired by the architecture of living organisms. The development of this new field of robotics is a medium-long term prospect but has the potential to revolutionise the manufacturing industry in the not-too-distant future. Our research is also of interest to those involved in the development of responsive nanomaterials and nanoreactors for sensing and drug delivery. Prof Helen Hailes: The findings from our research are expected to have non-academic impacts in the longer term. They are relevant to new enzyme applications, anti-TB drugs and the synthesis of new tetrahydroisoquinolines. 23 papers have been published. Prof Tom Sheppard (Department of Chemistry, UCL): 22 papers have already been published which are likely to have non-academic impacts in future. Our collaborations with AstraZeneca were extended via two new 3-year collaborative PDRA projects on catalytic amidation (related to 3 in Findings) and C-H activation (related to 4 in Findings). Prof Alethea Tabor (Department of Chemistry, UCL): Semiconducting polymer nanoparticles studied by us are used as novel contrast agents for photoacoustic and near infra-red imaging of tumours, which will allow for precision image-guided surgery of cancer patients. The findings of our research are therefore likely to have non-academic impacts. Dr Mukhlesur Rahman (School of Health, Sports and Bioscience, University of East London; Currently in Liverpool John Moores University): The research described in our publication titled "Terpenes from Zingiber montanum and Their Screening against Multi-Drug Resistant and Methicillin Resistant Staphylococcus aureus" will contribute towards the identification of lead anti-staphylococcal compounds. Mr Ryan Trueman (School of Pharmacy, UCL) and Dr Bob Schroeder (Department of Chemistry, UCL) have used the 700 MHz NMR to study metabolites secreted by therapeutic cells under electrical stimulation. Fane F. K. Mensah, PhD Candidate, and Prof Geraldine Cambridge (Division of Medicine, Centre of Rheumatology Research, UCL): The condition Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) has been poorly studied. Nevertheless, various publications have pointed to abnormalities in the immune system as well as in the metabolism of the patients. Our paper titled "CD24 Expression and B Cell Maturation Shows a Novel Link With Energy Metabolism: Potential Implications for Patients With Myalgic Encephalomyelitis/Chronic Fatigue Syndrome" contributed to both of these findings and has been very well received by both the scientific and patient community. Funding for biomedical research in ME/CFS has been very limited in both the UK and outside of the UK. Scientific research and publications, such as our paper, contribute towards a better understanding of ME/CFS and other diseases. Prof Junwang Tang and Dr Christopher Windle (Department of Chemical Engineering, UCL): In the long term the catalyst developed by us may find use in industrial methane reforming. We have already discovered the structure of the reaction products using the 700MHz facility, e.g., isotopic ammonia and molecular catalysts. It is very important to identify the final isotopic products in order to avoid misunderstanding the underlying chemical processes. Dr Simoni Da Ros and Dr Katherine Curran (Bartlett School Env, Energy & Resources, Faculty of the Built Environment, UCL): For the project dealing with historic plastics of cultural heritage significance, the findings are contributing to the knowledge exchange between universities and museums. Our work has been disseminated through non-academic channels such as the Institute of Conservation (ICON) website and the ICON News Magazine, where an article piece about our work was published in the magazine in April 2021. It is relevant to museums which house historic plastic artefacts, for better planning of their care. Using the 700MHz facility, we have shown that NMR spectroscopy can be successfully used to analyse the composition and degradation of historic plastic artefacts. Dr Stefan Howorka (Department of Chemistry, UCL): The research results are of potential interest to bioimaging and small-molecule probe development in the chemical/biotech industry. Prof Erik Arstad, Dr Thibault Gendon, Dr Fatih Srirndil and Dr Michael Porter (Institute of Nuclear Medicine, UCL and Department of Chemistry, UCL): We have developed a new type of leaving groups (dibenzothiophene sulfonium salts) for nucleophilic aromatic substitution, and have developed this as a platform for manufacturing of diagnostic positron emission tomography (PET) tracers. The chemistry is particularly relevant for PET chemistry, but we expect it will also find widespread use in synthetic chemistry as the leaving group we developed has been shown (by others) to be exceptionally well suited for Pd-couplings, i.e. allows coupling with 90% yield in the presence of aryl iodides Our findings have led to a £1.2 million grant from the MRC (subject to contract) for testing of a novel diagnostic tracer in humans for the first time. The 700MHz NMR instrument was used for recording quantitative 19F NMR spectra for the development of labelling chemistry of diagnostic tracers for imaging with PET. Dr Abil Aliev and Prof William Motherwell (Department of Chemistry, UCL): The work on noncovalent interactions promotes our understanding and controlling of three-dimensional molecular recognition in chemical reactions and biological processes, as well as in supramolecular chemistry, pharmaceutical sciences, host-guest complexation and crystal engineering. Prof Matthew Powner (Department of Chemistry, UCL): Published research results in such high-impact journals as Nature and Science. Advanced our understanding of the origins of life. They are also relevant to the pharmaceutical and fine chemical industries. Awards including Blavatnik Honoree 2021 (http://blavatnikawards.org/honorees/profile/matth ew-powner/) and RSC Harrison-Meldola Memorial Prize 2019 (https://www.rsc.org/prizes-funding/prizes/find-a- prize/harrison-meldola-memorial-prizes/previous-wi nners/). Our studies, which have used the 700MHz NMR facility and contributed significantly to the understanding of the emergence of life include: (1) We have reported the first prebiotic, chemoselective and stereospecific complete synthesis of (non-canonical) amino-nucleotide (See Whitaker & Powner Nat. Chem. 2022, accepted). Our results suggest that 3'-amino-threose nucleic acid (TNA) nucleosides may have been present on the early earth. (2) We have discovered a chemoselective peptide ligation in water (see Canavelli et al. Nature, 2019). (3) We have developed the first prebiotic synthesis of proteinogenic amino acid cysteine, via a novel nitrile mediated biomimetic reaction pathway (see Foden et al. Science, 2020). We have now shown that cysteine is a product of simple prebiotic chemistry. Our discovery supports the hypothesis that cysteine was simply a secondary product of serine chemistry at the origins of life. (4) We have discovered a novel protecting group-free, activating agent-free catalytic peptide ligation strategy that operates in neutral water (see Foden et al. published in Science, 2020). This work is relevant to green chemical strategies for synthesis and catalysis in water. (5) We have found that dipeptides derived from Ser, Thr and Asn undergo pronounced amidine hydrolysis to the corresponding peptides. Our data support a scenario in which nitriles served as an early energy currency on the primordial Earth, acting as a forerunner to ATP and thioesters that drive reactions in extant biology. (6) We have demonstrated diamidophosphate can be harnessed to achieve Strecker amino acid synthesis. The high yield of N-phosphoro-aminonitriles and their selective transformations provide new insights into prebiotic amino acid synthesis and activation. (7) We have developed a new method to achieve a divergent synthesis of purine and pyrimidine nucleotide with a common precursor (Roberts et al Nat. Commun 2018). (8) We have developed methods for the photochemical selection of nucleotide stereochemistry (Colville and Powner). (9) We have developed a new prebiotic strategy to access nucleotide 5'-phosphates in water. The new strategy opens new pathways to explore nucleotide syntheses and activations, which are closely aligned with the biochemical strategies exploited by extant life. (10) We have demonstrated that N-phospho-aminonitriles can not only be highly efficiently synthesised in neutral water but the neutral phosphorostrecker reaction provides excellent selectivity for proteinogenic amino acid (see Ashe et al in Nature - Communications Chemistry, 2019). (11) We have developed new chiral aldehydes for analysis and as standards to use for investigating the chemical composition of meteorite samples in collaboration with scientists at the Solar System Exploration Division, NASA Goddard Space Flight Center, USA (see Aponte et al in ACS Earth Space and Chemistry, 2019). (12) We have investigated the origins of Life on other planets (including Mars and current NASA missions of sample return) and explored exoplanet atmosphere and astrochemistry, developing green chemical strategies for synthesis and catalysis in water. Prof Jamie Baker's (Department of Chemistry, UCL): We have used findings from our research to develop reagents for the construction of next-generation protein conjugates, which can be employed for selective delivery of drugs, as well as for diagnostics. Dr Cally Haynes (Department of Chemistry, UCL): The expected long-term findings of our research are of interest to supramolecular chemistry, inorganic materials, soft materials, drug delivery and catalysis. Dr Gemma Louise-Davis (Department of Chemistry, UCL); Our findings are expected to have an impact on developing new precursors for high-signal MRI contrast agents, as well as on non-invasive disease diagnostics in clinical medicine, including diagnosis of bowel cancer. Prof Gopinathan Sankar (Department of Chemistry, UCL): Our work investigates the creation of macroporous silicalite material resulting in macropores within silicalite crystals and is relevant to materials chemistry and catalysis. Dr Joel Turner and Prof Gavin Jell (Royal Free Hospital, UCL): The findings from our research using 29Si NMR will impact studies of bone cell interactions with silicate species released from bioactive glasses. Dr Gareth Williams (School of Pharmacy, UCL): We have investigated perfluorophenyl azide functionalisation of biodegradable polymers, which is of interest to those working in the area of therapeutic protein delivery. Dr Stefan Guldin (Department of Chemical Engineering, UCL): Our findings are relevant to mesoporous inorganic thin films, which are promising materials for a variety of applications, including sensing, catalysis, protective coatings, energy generation and storage. Prof Ipsita Roy and Dr Pooja Bassnet (Department of Life Science, University of Westminster): We have investigated biodegradable polymers such as polyhydroxyalkanoates (PHAs). PHAs are used for a range of medical applications such as medical device development (coronary artery stents, nerve conduits, wound healing patches), tissue engineering scaffolds in Regenerative Medicine and controlled drug delivery. Dr Alistair Miller (Darr House and University of Exeter): The analysis carried out on the 700MHz NMR was used for the authentication of compounds for screening for insecticidal activity and is relevant to the agricultural section. Dr Will Travis (Gurit UK Ltd, Newport): The NMR spectra recorded on the 700MHz instrument helped develop materials for the composites industry with applications in predominately wind turbine and marine industries. The work is likely to reach the market soon. There are also impacts and research results of a confidential nature, details of which cannot be revealed here at this time.
First Year Of Impact 2015
Sector Agriculture, Food and Drink,Chemicals,Education,Electronics,Energy,Environment,Healthcare,Culture, Heritage, Museums and Collections,Pharmaceuticals and Medical Biotechnology
Impact Types Cultural

Societal

Economic

Policy & public services

 
Description NMR Metabonomics for the Diagnosis of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome by Researchers from UCL Centre of Rheumatology and New Zealand
Geographic Reach Multiple continents/international 
Policy Influence Type Influenced training of practitioners or researchers
 
Description Hub 'Science' 3: Catalysis for the Circular Economy and Sustainable Manufacturing
Amount £3,938,126 (GBP)
Funding ID EP/R027129/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 12/2018 
End 11/2024
 
Description Industrial CASE Award
Amount £69,524 (GBP)
Organisation Johnson Matthey 
Sector Private
Country United Kingdom
Start 01/2015 
End 01/2018
 
Description MilliKelvin Experiments Utilising Vector Magnetic Field
Amount £8,379 (GBP)
Funding ID EP/K040359/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 06/2013 
End 06/2015
 
Description Non-Ergodic Quantum Manipulation
Amount £7,032,540 (GBP)
Funding ID EP/R029075/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 01/2019 
End 12/2024
 
Description PicoFIB network: fundamentals of atom patterning using focused gas-ion beams
Amount £125,765 (GBP)
Organisation The Leverhulme Trust 
Sector Charity/Non Profit
Country United Kingdom
Start  
 
Description The UK Catalysis Hub - 'Science': 1 - Optimising, predicting and designing new Catalysts
Amount £3,683,534 (GBP)
Funding ID EP/R026815/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 12/2018 
End 11/2024
 
Description The UK Catalysis Hub - 'Science': 2 Catalysis at the Water-Energy Nexus
Amount £4,010,674 (GBP)
Funding ID EP/R026645/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 12/2018 
End 11/2024
 
Description The UK Catalysis Hub -'Core'
Amount £2,201,661 (GBP)
Funding ID EP/R026939/1 
Organisation Engineering and Physical Sciences Research Council (EPSRC) 
Sector Public
Country United Kingdom
Start 12/2018 
End 11/2024
 
Title XAFS DRIFTS methods 
Description WE have developed a flow system, gas handling and use of a DRIFS spectrometer in combination with XAFS ( at both diamond light source and ESRF) to study insitu and operando catalysis reactions looking at the reaction and structure of the catalysis to increase mechanistic and fundamental understanding of catalytic processes the expertise and equipment through BLock access to B18 on diamond light-source is now available as a resource for the community 
Type Of Material Improvements to research infrastructure 
Year Produced 2016 
Provided To Others? Yes  
Impact A number of publications have arisen from this research tool, additional funding for development of a flow Cell as been secured as an INDUSTRIAL CASE award 
 
Title NMR Chemical shift anisotropy measurements 
Description Using 300 MHz and 700 MHz NMR instruments, it has been shown that static lineshape measurements are better suited for accurate measurements of the chemical shift anisotropy than those based on magic-angle spinning. 
Type Of Material Data analysis technique 
Year Produced 2017 
Provided To Others? Yes  
Impact Accurate measurements of chemical shift anisotropy is important for materials, chemistry and biological sciences. 
URL https://www.sciencedirect.com/science/article/pii/S0926204017301303?via=ihub
 
Title X-ray Tomography of N95 Face Mask 
Description The N95 mask sample was scanned by lab-based X-ray micro-scale CT scanner (Zeiss Xradia 620 Versa, Carl Zeiss Inc.). 501 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 350 nm with the narrower (ca. 350 µm x 350 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_Tomography_of_N95_Face_Mask/13308488
 
Title X-ray Tomography of N95 Face Mask 
Description The N95 mask sample was scanned by lab-based X-ray micro-scale CT scanner (Zeiss Xradia 620 Versa, Carl Zeiss Inc.). 501 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 350 nm with the narrower (ca. 350 µm x 350 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_Tomography_of_N95_Face_Mask/13308488/2
 
Title X-ray Tomography of N95 Face Mask 
Description The N95 mask sample was scanned by lab-based X-ray micro-scale CT scanner (Zeiss Xradia 620 Versa, Carl Zeiss Inc.). 501 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 350 nm with the narrower (ca. 350 µm x 350 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2020 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_Tomography_of_N95_Face_Mask/13308488/1
 
Title X-ray nano CT of Carbon-Sulfur Cathode@1st Cycle ChargeState 
Description The S/C cathode was scanned by lab-based X-ray nano-scale CT scanner (Zeiss Xradia 810 Ultra, Carl Zeiss Inc.). 1601 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 126 nm with the narrower (64 µm x 64 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_nano_CT_of_Carbon-Sulfur_Cathode_1st_Cycle_ChargeState/...
 
Title X-ray nano CT of Carbon-Sulfur Cathode@1st Cycle ChargeState 
Description The S/C cathode was scanned by lab-based X-ray nano-scale CT scanner (Zeiss Xradia 810 Ultra, Carl Zeiss Inc.). 1601 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 126 nm with the narrower (64 µm x 64 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_nano_CT_of_Carbon-Sulfur_Cathode_1st_Cycle_ChargeState/...
 
Title X-ray nano CT of Carbon-Sulfur Cathode@3rd Cycle ChargeState 
Description The S/C cathode was scanned by lab-based X-ray nano-scale CT scanner (Zeiss Xradia 810 Ultra, Carl Zeiss Inc.). 1601 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 126 nm with the narrower (64 µm x 64 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_nano_CT_of_Carbon-Sulfur_Cathode_3rd_Cycle_ChargeState/...
 
Title X-ray nano CT of Carbon-Sulfur Cathode@3rd Cycle ChargeState 
Description The S/C cathode was scanned by lab-based X-ray nano-scale CT scanner (Zeiss Xradia 810 Ultra, Carl Zeiss Inc.). 1601 projections were obtained for the specimen. The standard reconstruction algorithm is used to reconstruct sample. The voxel resolution at 126 nm with the narrower (64 µm x 64 µm) field of view was achieved. 
Type Of Material Database/Collection of data 
Year Produced 2021 
Provided To Others? Yes  
URL https://rdr.ucl.ac.uk/articles/dataset/X-ray_nano_CT_of_Carbon-Sulfur_Cathode_3rd_Cycle_ChargeState/...
 
Description Aliphatic Aldehydes and Ketones in Carbonaceous Chondrites (Matt Powner) 
Organisation Ludwig Maximilian University of Munich (LMU Munich)
Country Germany 
Sector Academic/University 
PI Contribution NMR analysis.
Collaborator Contribution Sample provision for analysis.
Impact Publication: "Analyses of Aliphatic Aldehydes and Ketones in Carbonaceous Chondrites" José C. Aponte*, Daniel Whitaker, Matthew W. Powner, Jamie E. Elsila, and Jason P. Dworkin, ACS Earth Space Chem. 2019, 3, 3, 463-472 Publication Date:February 20, 2019. https://doi.org/10.1021/acsearthspacechem.9b00006
Start Year 2017
 
Description Aliphatic Aldehydes and Ketones in Carbonaceous Chondrites (Matt Powner) 
Organisation National Aeronautics and Space Administration (NASA)
Department Goddard Space Flight Center
Country United States 
Sector Public 
PI Contribution NMR analysis.
Collaborator Contribution Sample provision for analysis.
Impact Publication: "Analyses of Aliphatic Aldehydes and Ketones in Carbonaceous Chondrites" José C. Aponte*, Daniel Whitaker, Matthew W. Powner, Jamie E. Elsila, and Jason P. Dworkin, ACS Earth Space Chem. 2019, 3, 3, 463-472 Publication Date:February 20, 2019. https://doi.org/10.1021/acsearthspacechem.9b00006
Start Year 2017
 
Description Antiviral targets and gene therapy (David Selwood) 
Organisation University College London
Department Division of Infection and Immunity
Country United Kingdom 
Sector Academic/University 
PI Contribution David Selwood: Working with Greg Towers (I&I, UCL) we have discovered that carefully optimised cyclosporine derivatives can block HIV and other viruses' replication. Gene delivery uses modified, safe HIV-vector based on the virus. HIV can efficiently deliver genes to target cells but unfortunately human stem cells are quite resistant to infection. Thus, a major hurdle in the clinical application of stem cell gene therapy is achieving sufficient modification to maximise clinical benefit. HIV-vector production costs ~£100,000's for a single trial. We have discovered that a significant block to stem cell infection can be circumvented using these derivatives and this is a focus of current research. We have achieved notable grant success for this area with > £4million raised (see funding section).
Collaborator Contribution Infection studies
Impact Che C Colpitts, Sophie Ridewood, Bethany Schneiderman, Justin Warne, Keisuke Tabata, Caitlin F Ng, Ralf Bartenschlager, David L Selwood, Greg J Towers Hepatitis C virus exploits cyclophilin A to evade PKR Elife 2020 Jun 16;9:e52237. doi: 10.7554/eLife.52237. Counteracting innate immunity is essential for successful viral replication. Host cyclophilins (Cyps) have been implicated in viral evasion of host antiviral responses, although the mechanisms are still unclear. Here, we show that hepatitis C virus (HCV) co-opts the host protein CypA to aid evasion of antiviral responses dependent on the effector protein kinase R (PKR). Pharmacological inhibition of CypA rescues PKR from antagonism by HCV NS5A, leading to activation of an interferon regulatory factor-1 (IRF1)-driven cell intrinsic antiviral program that inhibits viral replication. These findings further the understanding of the complexity of Cyp-virus interactions, provide mechanistic insight into the remarkably broad antiviral spectrum of Cyp inhibitors, and uncover novel aspects of PKR activity and regulation. Collectively, our study identifies a novel antiviral mechanism that harnesses cellular antiviral immunity to suppress viral replication. We were the first group to show that a host-directed PROTAC could have antiviral activity.
Start Year 2020
 
Description C*Change Catalysis Network south africa 
Organisation University of Cape Town
Department Department of Oceanography
Country South Africa 
Sector Academic/University 
PI Contribution Organisation of network meeting between C*Change members and the Catalysis Hub leading to at least one Diamond beam line experiment as a collaboration (results pending)
Collaborator Contribution intellect input and samples of collaborative experiments for Catalysis using Diamond lightsource
Impact succesful beam time applications
Start Year 2015
 
Description COMPLEX: The Degradation of Complex Modern Polymeric Objects in Heritage Collections: A System Dynamics Approach. 
Organisation University College London
Country United Kingdom 
Sector Academic/University 
PI Contribution Dr Simoni Ros collaborates with the UCL Institute for Sustainable Heritage in a research project named as COMPLEX: The Degradation of Complex Modern Polymeric Objects in Heritage Collections: A System Dynamics Approach. This project is led by Professor Associate Dr Katherine Curran, principal investigator and responsible for acquiring the starting grant from the European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme (grant agreement No 716390).
Collaborator Contribution From the collaboration named above, a new MSc project has been started in the UCL MSc Applied Analytical Chemistry, in which the student Luka Nunar will explore NMR spectroscopy to develop new methodologies for the quantification of plasticiser contents and the degradation extent in historic plasticised artifacts based on solution and solid-state 1H and 13C NMR techniques. The UCL 700 MHz NMR facility has also contributed to two MRes dissertation projects from the UCL Institute for Sustainable Heritage, involving the students Isabella del Gaudio (title: Study of water sorption and diffusion in cellulose acetate) and Rose King (title: Plasticiser loss from cellulose acetate), which have investigated degradation processes of cellulose acetate, involving the investigation of deacetylation and plasticiser loss. The research has evolved in PhD projects involving the same students and both projects currently benefit from their use of the UCL 700 MHz NMR facility.
Impact In preparation for submission in the Polymer Degradation and Stability journal: "Quantifying the degradation state of plasticised cellulose acetate-based historic artefacts by NMR spectroscopy", by Simoní Da Ros, Abil E. Aliev, Isabella del Gaudio, Rose King, Anna Pokorska, Mark Kearney, Katherine Curran. Argyro Gili, Rose King, Luca Mazzei, Josep Grau-Bové, Robert Koestler, Michael Petr, Odile Madden, Simoní Da Ros, Katherine Curran. Modelling and Measuring the Diethyl Phthalate Plasticiser loss from Cellulose Acetate in different ventilation scenarios. Presented at "The Plastics Heritage Congress 2019", Lisbon, 2019. (Oral presentation) Del Gaudio I, Hunter-Sellars E, Da Ros S, Parkin I, Duncan J, Moore A, Williams D, Curran K. Stability of cellulose acetate films in museum collections. Presented at "The Polymer Degradation Discussion Group Conference", Malta, 2019. (Poster presentation) Argyro Gili, Rose King, Luca Mazzei, Simoní Da Ros, Josep Grau-Bové, Robert Koestler, Michael Petr, Odile Madden, Katherine Curran. A Predictive Model and Measurements for the Impact of Ventilation on Diethyl Phthalate Plasticiser Loss from Cellulose Acetate. Presented at the "Plastics and Peril Conference", Cambridge, 2020. (Poster presentation) Argyro Gili, Rose King, Luca Mazzei, Simoní Da Ros, Josep Grau-Bové, Robert, Koestler, Michael Petr, Odile Madden, Katherine Curran. Decision making in conservation based on modelling and measuring diethyl phthalate plasticiser loss from cellulose acetate in varied ventilation conditions. Presented at the "Plastics and Peril Conference", Cambridge, 2020. (Oral presentation)
Start Year 2019
 
Description Collaboration with ISIS neutron and muon source and Johnson Matthe and development of a special edition of PCCP 
Organisation Johnson Matthey
Country United Kingdom 
Sector Private 
PI Contribution In association with ISIS the Hub held a workshop on, "Neutron Techniques in Catalysis" in Nov 2014. There were a mix of delegates from industry and academia, with over fifty attendees. This helped to provide training and knowledge transfer to catalytic community who may previously not have used neutrons leading to a range of new users including Johnson Matthey, Academics from Southampton university and UCL. Following this workshop scientists from ISIS, The Catalysis Hub and Johnson Matthey proposed and led a special issue of PCCP edition, "Neutron scattering in catalysis and energy materials"
Collaborator Contribution talks and co organsiation of papers, "Neutron Techniques in Catalysis" in Nov 2014 knowledge and interaction and the contribution of papers and newtork expertise for special issue of PCCP edition, "Neutron scattering in catalysis and energy materials"
Impact special edition of PCCP Neutron scattering in catalysis and energy materials" and increasing use of ISIS beamtime for catalysis research and recognition of the importance of neutron techniques for Johnson matthey (industrial) especially in the region of automotive catalysis and Selective catalytic reduction
Start Year 2015
 
Description Collaboration with ISIS neutron and muon source and Johnson Matthe and development of a special edition of PCCP 
Organisation Science and Technologies Facilities Council (STFC)
Department ISIS Neutron and Muon Source
Country United Kingdom 
Sector Academic/University 
PI Contribution In association with ISIS the Hub held a workshop on, "Neutron Techniques in Catalysis" in Nov 2014. There were a mix of delegates from industry and academia, with over fifty attendees. This helped to provide training and knowledge transfer to catalytic community who may previously not have used neutrons leading to a range of new users including Johnson Matthey, Academics from Southampton university and UCL. Following this workshop scientists from ISIS, The Catalysis Hub and Johnson Matthey proposed and led a special issue of PCCP edition, "Neutron scattering in catalysis and energy materials"
Collaborator Contribution talks and co organsiation of papers, "Neutron Techniques in Catalysis" in Nov 2014 knowledge and interaction and the contribution of papers and newtork expertise for special issue of PCCP edition, "Neutron scattering in catalysis and energy materials"
Impact special edition of PCCP Neutron scattering in catalysis and energy materials" and increasing use of ISIS beamtime for catalysis research and recognition of the importance of neutron techniques for Johnson matthey (industrial) especially in the region of automotive catalysis and Selective catalytic reduction
Start Year 2015
 
Description Collaboration with Johnson Matthey 
Organisation Johnson Matthey
Country United Kingdom 
Sector Private 
PI Contribution The research team have approached Johnson Matthey in order to gain an industrial input, as part of an ongoing collaboration.
Collaborator Contribution Contact between Johnson Matthey and the investigators of this project are helping to direct research towards areas of industrial interest.
Impact This collaboration has lead to the inclusion of industrial expertise into our research planing.
Start Year 2016
 
Description Collaboration with Johnson Matthey 
Organisation Johnson Matthey
Country United Kingdom 
Sector Private 
PI Contribution Johnson Matthey have placed a research fellow within the catalysis hub which has lead to a number of scientific advancements for both parties, , and events including the neutrons for catalysis workshop whihc was run between Johnson Matthey, the UK catalysis Hub and ISIS. Collaborations with the UK catalysis HUb ave lead to Johnson Matheys having increased interaction with Diamond and ISIS and CLF including developing new capability and discovering new techniques. It also lead to the appopintment of a IMPACT fellow from Johnson Matthey ~( Rachel O'malley) as part of the Impact acceleeration grant
Collaborator Contribution JM have provided materials precursors and contrbuted to a number of projects intallectualy and finacially including awarding of several case Phd Projects
Impact Chemistry, materials science
Start Year 2014
 
Description Combined high resolution x-ray and DFT Bader analysis to reveal a proposed Ru-H ··· Si interaction in Cp(IPr)Ru(H)2SiH(Ph)Cl 
Organisation Diamond Light Source
Country United Kingdom 
Sector Private 
PI Contribution Multinuclear 1H, 13C and 29Si NMR measurements and analysis.
Collaborator Contribution DFT calculations
Impact This collaboration has led to a publication.
Start Year 2018
 
Description Combined high resolution x-ray and DFT Bader analysis to reveal a proposed Ru-H ··· Si interaction in Cp(IPr)Ru(H)2SiH(Ph)Cl 
Organisation Rutherford Appleton Laboratory
Country United Kingdom 
Sector Academic/University 
PI Contribution Multinuclear 1H, 13C and 29Si NMR measurements and analysis.
Collaborator Contribution DFT calculations
Impact This collaboration has led to a publication.
Start Year 2018
 
Description Combined high resolution x-ray and DFT Bader analysis to reveal a proposed Ru-H ··· Si interaction in Cp(IPr)Ru(H)2SiH(Ph)Cl (Abil Aliev) 
Organisation Francis Crick Institute
Country United Kingdom 
Sector Academic/University 
PI Contribution Multinuclear 1H, 13C and 29Si NMR measurements and analysis.
Collaborator Contribution DFT calculations
Impact This collaboration has led to a publication,
Start Year 2018
 
Description DENSsolutions 
Organisation DENSsolutions BV
Country Netherlands 
Sector Private 
PI Contribution Conformational studies on Ferritin and RNAp proteins via in-situ liquid heating TEM
Collaborator Contribution DENSs contributed to the project by lending us the liquid heating unit that was used for the experiment. The company also provided some liquid cells needed for imaging
Impact Not yet, experiments were interrupted by COVID
Start Year 2020
 
Description Development of XAFS methods for industrial applications 
Organisation Diamond Light Source
Country United Kingdom 
Sector Private 
PI Contribution Technique development for Combined Drifts experiments
Collaborator Contribution Comisioning Time, Beam time and Intellectual expertise, Funding for a studentship
Impact New IR suite at Research complex Publications (already included on the grant portfolio) DOI: 10.1016/j.jcat.2019.03.037, DOI: 10.1038/s41929-018-0213-3 DOI: 10.1021/acs.chemmater.7b02552
Start Year 2013
 
Description Development of XAFS methods for industrial applications 
Organisation Johnson Matthey
Country United Kingdom 
Sector Private 
PI Contribution Technique development for Combined Drifts experiments
Collaborator Contribution Comisioning Time, Beam time and Intellectual expertise, Funding for a studentship
Impact New IR suite at Research complex Publications (already included on the grant portfolio) DOI: 10.1016/j.jcat.2019.03.037, DOI: 10.1038/s41929-018-0213-3 DOI: 10.1021/acs.chemmater.7b02552
Start Year 2013
 
Description Development of XAFS methods for industrial applications 
Organisation Queen's University Belfast
Country United Kingdom 
Sector Academic/University 
PI Contribution Technique development for Combined Drifts experiments
Collaborator Contribution Comisioning Time, Beam time and Intellectual expertise, Funding for a studentship
Impact New IR suite at Research complex Publications (already included on the grant portfolio) DOI: 10.1016/j.jcat.2019.03.037, DOI: 10.1038/s41929-018-0213-3 DOI: 10.1021/acs.chemmater.7b02552
Start Year 2013
 
Description Development of XAFS methods for industrial applications 
Organisation University of Glasgow
Country United Kingdom 
Sector Academic/University 
PI Contribution Technique development for Combined Drifts experiments
Collaborator Contribution Comisioning Time, Beam time and Intellectual expertise, Funding for a studentship
Impact New IR suite at Research complex Publications (already included on the grant portfolio) DOI: 10.1016/j.jcat.2019.03.037, DOI: 10.1038/s41929-018-0213-3 DOI: 10.1021/acs.chemmater.7b02552
Start Year 2013
 
Description Development of XAFS methods for industrial applications 
Organisation University of Manchester
Country United Kingdom 
Sector Academic/University 
PI Contribution Technique development for Combined Drifts experiments
Collaborator Contribution Comisioning Time, Beam time and Intellectual expertise, Funding for a studentship
Impact New IR suite at Research complex Publications (already included on the grant portfolio) DOI: 10.1016/j.jcat.2019.03.037, DOI: 10.1038/s41929-018-0213-3 DOI: 10.1021/acs.chemmater.7b02552
Start Year 2013
 
Description Development of XAFS methods for industrial applications 
Organisation University of Southampton
Country United Kingdom 
Sector Academic/University 
PI Contribution Technique development for Combined Drifts experiments
Collaborator Contribution Comisioning Time, Beam time and Intellectual expertise, Funding for a studentship
Impact New IR suite at Research complex Publications (already included on the grant portfolio) DOI: 10.1016/j.jcat.2019.03.037, DOI: 10.1038/s41929-018-0213-3 DOI: 10.1021/acs.chemmater.7b02552
Start Year 2013
 
Description Dr Samuel Sanchez 
Organisation Institute for Bioengineering of Catalonia
Country Spain 
Sector Private 
PI Contribution Inorganic nanomotors , a study by Liquid TEM
Collaborator Contribution Inorganic nanomotors , a study by Liquid TEM
Impact Manuscript in preparation
Start Year 2019
 
Description Dr Xavier Salvatella 
Organisation Institute for Research in Biomedicine (IRB)
Country Spain 
Sector Academic/University 
PI Contribution Phase separation properties of Intrinsically disordered protein CPEB4 linked to Autism disorder imaged by Liquid TEM
Collaborator Contribution Phase separation properties of Intrinsically disordered protein CPEB4 linked to Autism disorder imaged by Liquid TEM
Impact Not yet
Start Year 2018
 
Description Dr Zoe Waller 
Organisation University College London
Department School of Pharmacy
Country United Kingdom 
Sector Academic/University 
PI Contribution DNA conformational studies. Dr Waller will need to secure some funding for covering the service expenses. This collaboration or partnership if initiated will bring a direct financial contribution to our research. This partnership will be in the form of imaging service.
Collaborator Contribution Dr Waller will need to secure some funding for covering the service expenses. This collaboration or partnership if initiated will bring a direct financial contribution to our research. This partnership will be in the form of imaging service.
Impact A first imaging session has been performed to prove suitability of the technique for investigating DNA via liquid TEM. No outcomes yet.
Start Year 2020
 
Description Drugs for treatment of neurodegenerative diseases 
Organisation Dementia Discovery Fund
Country United Kingdom 
Sector Private 
PI Contribution Compounds are sought for use as inhibitors of key targets for treatment of neurodegenerative diseases such as neurodegeneration, Alzheimer's disease and dementia. The 700MHz NMR facility is used for structural characterisation of newly synthesised compounds.
Collaborator Contribution Dementia Discovery Fund is a spin out company.
Impact The following publications are relevant: Beilstein J. Org. Chem. 2019, 15, 2790-2797. doi:10.3762/bjoc.15.271 Med. Chem. Commun. 2019, 10, 1361 DOI: 10.1039/c9md00096h
Start Year 2019
 
Description Drugs for treatment of neurodegenerative diseases (Paul Fish, Alz) 
Organisation Dementia Discovery Fund
Country United Kingdom 
Sector Private 
PI Contribution Compounds are sought for use as inhibitors of key targets for treatment of neurodegenerative diseases such as neurodegeneration, Alzheimer's disease and dementia. The 700MHz NMR facility is used for structural characterisation of newly synthesised compounds.
Collaborator Contribution Dementia Discovery Fund is a spin out company.
Impact The following publications are relevant: Beilstein J. Org. Chem. 2019, 15, 2790-2797. doi:10.3762/bjoc.15.271 Med. Chem. Commun. 2019, 10, 1361 DOI: 10.1039/c9md00096h
Start Year 2019
 
Description EGFR-Targeted Semiconducting Polymer Nanoparticles for Photoacoustic Imaging 
Organisation University of Cambridge
Department Department of Chemistry
Country United Kingdom 
Sector Academic/University 
PI Contribution We have prepared novel semiconducting polymer nanoparticles for photoacoustic imaging, conjugated to peptides targeted to cancer cells. As part of this, we have developed a novel NMR approach to characterise the level of bioconjugation of the targeting peptides to the nanoparticles.
Collaborator Contribution Preparation of semiconducting polymer nanoparticles.
Impact A manuscript is currently under preparation.
Start Year 2019
 
Description EGFR-Targeted Semiconducting Polymer Nanoparticles for Photoacoustic Imaging 
Organisation University of Cambridge
Department Department of Chemistry
Country United Kingdom 
Sector Academic/University 
PI Contribution We have prepared novel semiconducting polymer nanoparticles for photoacoustic imaging, conjugated to peptides targeted to cancer cells. As part of this, we have developed a novel NMR approach to characterise the level of bioconjugation of the targeting peptides to the nanoparticles.
Collaborator Contribution Preparation of semiconducting polymer nanoparticles.
Impact A manuscript is currently under preparation.
Start Year 2019
 
Description Mechanistic study of boron-catalysed amidation reactions (Tom Sheppard) 
Organisation AstraZeneca
Department Research and Development AstraZeneca
Country United Kingdom 
Sector Private 
PI Contribution In 2021, Prof Tom Sheppard (UCL Chemistry) and others have begun a new EPSRC-funded project on the mechanistic study of boron-catalysed amidation reactions (EP/T030488/1) in collaboration with Professor Andy Whiting (Durham University), Professor Henry Rzepa (Imperial College London), Dr Jordi Burés (University of Manchester) and scientists from GSK, AstraZeneca & Syngenta. This project will make extensive use of the 700 MHz NMR for elucidating the structures of novel catalysts and potential reaction intermediates. Previous work in this area (outlined above in (1) in Findings) also led to funding for a 3-year collaborative PDRA with AstraZeneca. The study of boron-mediated reactions in organic synthesis and reactions of organoboron compounds was undertaken by the use of 11B NMR. We have shown that greater insight into the structures present in such systems can be obtained by using DFT chemical shift calculations to support or exclude proposed reaction intermediates.
Collaborator Contribution AstraZeneca has funded two 3-year PDRAs based at Macclesfield (the PDRAs are AZ employees). These are linked to the amidation (EPSRC EP/T030488/1) and the CH-Activation projects.
Impact Publications: C. E. Coomber, M. J. Porter, A. E. Aliev, P. D. Smith, T. D. Sheppard, Tuning Reactivity in Pd-Catalysed C(sp3)-H Arylations via Directing Group Modifications and Solvent Selection, Advanced Synthesis & Catalysis 2020, 362, 5105. doi: 10.1002/adsc.202000726 Arkhipenko S, Sabatini MT, Batsanov AS, Karaluka V, Sheppard TD, Rzepa HS, ... Whiting A. (2018). Mechanistic insights into boron-catalysed direct amidation reactions. Chemical science, 9(4), pp. 1058-1072. Coomber CE, Laserna V, Martin LT, Smith PD, Hailes HC, Porter MJ, ... Sheppard TD. (2019). Catalytic direct amidations in tert-butyl acetate using B(OCHCF). Organic & biomolecular chemistry, 17(26), pp. 6465-6469. doi: 10.1039/C9OB01012B Rzepa HS, Arkhipenko S, Wan E, Sabatini MT, Karaluka V, Whiting A, ... Sheppard TD. (2018). An Accessible Method for DFT Calculation of B NMR Shifts of Organoboron Compounds. The Journal of organic chemistry, 83(15), pp. 8020-8025. doi: 10.1021/acs.joc.8b00859 Sabatini MT, Boulton LT, Sheppard TD. (2017). Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science advances, 3(9), pp. e1701028. doi: 10.1126/sciadv.1701028 Sabatini MT, Karaluka V, Lanigan RM, Boulton LT, Badland M, Sheppard TD. (2018). Protecting-Group-Free Amidation of Amino Acids using Lewis Acid Catalysts. Chemistry (Weinheim an der Bergstrasse, Germany), 24(27), pp. 7033-7043. doi: 10.1002/chem.201800372
Start Year 2021
 
Description Mechanistic study of boron-catalysed amidation reactions (Tom Sheppard) 
Organisation GlaxoSmithKline (GSK)
Department GlaxoSmithKline Medicines Research Centre
Country United Kingdom 
Sector Private 
PI Contribution In 2021, Prof Tom Sheppard (UCL Chemistry) and others have begun a new EPSRC-funded project on the mechanistic study of boron-catalysed amidation reactions (EP/T030488/1) in collaboration with Professor Andy Whiting (Durham University), Professor Henry Rzepa (Imperial College London), Dr Jordi Burés (University of Manchester) and scientists from GSK, AstraZeneca & Syngenta. This project will make extensive use of the 700 MHz NMR for elucidating the structures of novel catalysts and potential reaction intermediates. Previous work in this area (outlined above in (1) in Findings) also led to funding for a 3-year collaborative PDRA with AstraZeneca. The study of boron-mediated reactions in organic synthesis and reactions of organoboron compounds was undertaken by the use of 11B NMR. We have shown that greater insight into the structures present in such systems can be obtained by using DFT chemical shift calculations to support or exclude proposed reaction intermediates.
Collaborator Contribution AstraZeneca has funded two 3-year PDRAs based at Macclesfield (the PDRAs are AZ employees). These are linked to the amidation (EPSRC EP/T030488/1) and the CH-Activation projects.
Impact Publications: C. E. Coomber, M. J. Porter, A. E. Aliev, P. D. Smith, T. D. Sheppard, Tuning Reactivity in Pd-Catalysed C(sp3)-H Arylations via Directing Group Modifications and Solvent Selection, Advanced Synthesis & Catalysis 2020, 362, 5105. doi: 10.1002/adsc.202000726 Arkhipenko S, Sabatini MT, Batsanov AS, Karaluka V, Sheppard TD, Rzepa HS, ... Whiting A. (2018). Mechanistic insights into boron-catalysed direct amidation reactions. Chemical science, 9(4), pp. 1058-1072. Coomber CE, Laserna V, Martin LT, Smith PD, Hailes HC, Porter MJ, ... Sheppard TD. (2019). Catalytic direct amidations in tert-butyl acetate using B(OCHCF). Organic & biomolecular chemistry, 17(26), pp. 6465-6469. doi: 10.1039/C9OB01012B Rzepa HS, Arkhipenko S, Wan E, Sabatini MT, Karaluka V, Whiting A, ... Sheppard TD. (2018). An Accessible Method for DFT Calculation of B NMR Shifts of Organoboron Compounds. The Journal of organic chemistry, 83(15), pp. 8020-8025. doi: 10.1021/acs.joc.8b00859 Sabatini MT, Boulton LT, Sheppard TD. (2017). Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science advances, 3(9), pp. e1701028. doi: 10.1126/sciadv.1701028 Sabatini MT, Karaluka V, Lanigan RM, Boulton LT, Badland M, Sheppard TD. (2018). Protecting-Group-Free Amidation of Amino Acids using Lewis Acid Catalysts. Chemistry (Weinheim an der Bergstrasse, Germany), 24(27), pp. 7033-7043. doi: 10.1002/chem.201800372
Start Year 2021
 
Description Mechanistic study of boron-catalysed amidation reactions (Tom Sheppard) 
Organisation Sengenia Ltd
Country United Kingdom 
Sector Private 
PI Contribution In 2021, Prof Tom Sheppard (UCL Chemistry) and others have begun a new EPSRC-funded project on the mechanistic study of boron-catalysed amidation reactions (EP/T030488/1) in collaboration with Professor Andy Whiting (Durham University), Professor Henry Rzepa (Imperial College London), Dr Jordi Burés (University of Manchester) and scientists from GSK, AstraZeneca & Syngenta. This project will make extensive use of the 700 MHz NMR for elucidating the structures of novel catalysts and potential reaction intermediates. Previous work in this area (outlined above in (1) in Findings) also led to funding for a 3-year collaborative PDRA with AstraZeneca. The study of boron-mediated reactions in organic synthesis and reactions of organoboron compounds was undertaken by the use of 11B NMR. We have shown that greater insight into the structures present in such systems can be obtained by using DFT chemical shift calculations to support or exclude proposed reaction intermediates.
Collaborator Contribution AstraZeneca has funded two 3-year PDRAs based at Macclesfield (the PDRAs are AZ employees). These are linked to the amidation (EPSRC EP/T030488/1) and the CH-Activation projects.
Impact Publications: C. E. Coomber, M. J. Porter, A. E. Aliev, P. D. Smith, T. D. Sheppard, Tuning Reactivity in Pd-Catalysed C(sp3)-H Arylations via Directing Group Modifications and Solvent Selection, Advanced Synthesis & Catalysis 2020, 362, 5105. doi: 10.1002/adsc.202000726 Arkhipenko S, Sabatini MT, Batsanov AS, Karaluka V, Sheppard TD, Rzepa HS, ... Whiting A. (2018). Mechanistic insights into boron-catalysed direct amidation reactions. Chemical science, 9(4), pp. 1058-1072. Coomber CE, Laserna V, Martin LT, Smith PD, Hailes HC, Porter MJ, ... Sheppard TD. (2019). Catalytic direct amidations in tert-butyl acetate using B(OCHCF). Organic & biomolecular chemistry, 17(26), pp. 6465-6469. doi: 10.1039/C9OB01012B Rzepa HS, Arkhipenko S, Wan E, Sabatini MT, Karaluka V, Whiting A, ... Sheppard TD. (2018). An Accessible Method for DFT Calculation of B NMR Shifts of Organoboron Compounds. The Journal of organic chemistry, 83(15), pp. 8020-8025. doi: 10.1021/acs.joc.8b00859 Sabatini MT, Boulton LT, Sheppard TD. (2017). Borate esters: Simple catalysts for the sustainable synthesis of complex amides. Science advances, 3(9), pp. e1701028. doi: 10.1126/sciadv.1701028 Sabatini MT, Karaluka V, Lanigan RM, Boulton LT, Badland M, Sheppard TD. (2018). Protecting-Group-Free Amidation of Amino Acids using Lewis Acid Catalysts. Chemistry (Weinheim an der Bergstrasse, Germany), 24(27), pp. 7033-7043. doi: 10.1002/chem.201800372
Start Year 2021
 
Description Metagenomic ene-reductases for the bioreduction of sterically challenging enones 
Organisation Almac Group
Country United Kingdom 
Sector Private 
PI Contribution Prof H. Hailes (Department of Chemistry, UCL), Dr J. Ward (Biochemical Engineering, UCL), Dr C. Orengo (Structural and Molecular Biology, UCL) and Dr Tom Moody (Almac) are involved in this collaboration. The 700MHz facility was essential to determine the stereochemistry of ene-reductase enzyme products. In this work, a sequence-based functional metagenomics strategy was used to identify novel ene-reductase enzymes from a drain metagenome. Several new ene-reductases were discovered and effectively applied in the stereoselective bioreduction of bicyclic Wieland-Miescher and Hajos-Parish ketones. Notably, this is the first time such bulky substrates have been successfully transformed with wild-type ene-reductases and the enzymes also showed remarkable organic solvent robustness which is ideal for industrial applications. Funding BBRSC BB/N01877X/1 & BB/L007444/1
Collaborator Contribution The enzymes prepared by Prof H. Hailes (Department of Chemistry, UCL), Dr J. Ward (Biochemical Engineering, UCL) and Dr C. Orengo (Structural and Molecular Biology, UCL) are used in the company. For detailed description, see D. Dobrijevic, L. Benhamou, A. E. Aliev, N. Dawson, D. Baud, D. Méndez Sánchez, N. Tappertzhofen, T. S. Moody, C. A. Orengo, H. C. Hailes, J. M. Ward, 'Ene-reductases from a drain metagenome for the selective bioreduction of bicyclic enones', RSC Adv., 2019, 9, 36608-36614. A new iCASE studentship was also funded starting in Sept 2020 on a new enzyme type. Another grant application has been submitted by Prof H Hailes (UCL) together with Almac. There are contracts that were signed (with Biochemical Engineering, UCL) with MTAs included and materials (enzymes) were transferred that are being used in commercial applications. Almac contributed £132k and an industrial perspective/time at attendance for meetings, etc.
Impact Publication in RSC Advances in 2019: D. Dobrijevic, L. Benhamou, A. E. Aliev, N. Dawson, D. Baud, D. Méndez Sánchez, N. Tappertzhofen, T. S. Moody, C. A. Orengo, H. C. Hailes, J. M. Ward, 'Ene-reductases from a drain metagenome for the selective bioreduction of bicyclic enones', RSC Adv., 2019, 9, 36608-36614.
Start Year 2017
 
Description Metagenomic ene-reductases for the bioreduction of sterically challenging enones (Helen Hailes) 
Organisation Almac Group
Country United Kingdom 
Sector Private 
PI Contribution Prof H. Hailes (Department of Chemistry, UCL), Dr J. Ward (Biochemical Engineering, UCL), Dr C. Orengo (Structural and Molecular Biology, UCL) and Dr Tom Moody (Almac) are involved in this collaboration. The 700MHz facility was essential to determine the stereochemistry of ene-reductase enzyme products. In this work, a sequence-based functional metagenomics strategy was used to identify novel ene-reductase enzymes from a drain metagenome. Several new ene-reductases were discovered and effectively applied in the stereoselective bioreduction of bicyclic Wieland-Miescher and Hajos-Parish ketones. Notably, this is the first time such bulky substrates have been successfully transformed with wild-type ene-reductases and the enzymes also showed remarkable organic solvent robustness which is ideal for industrial applications. Funding BBRSC BB/N01877X/1 & BB/L007444/1
Collaborator Contribution The enzymes prepared by Prof H. Hailes (Department of Chemistry, UCL), Dr J. Ward (Biochemical Engineering, UCL) and Dr C. Orengo (Structural and Molecular Biology, UCL) are used in the company. For detailed description, see D. Dobrijevic, L. Benhamou, A. E. Aliev, N. Dawson, D. Baud, D. Méndez Sánchez, N. Tappertzhofen, T. S. Moody, C. A. Orengo, H. C. Hailes, J. M. Ward, 'Ene-reductases from a drain metagenome for the selective bioreduction of bicyclic enones', RSC Adv., 2019, 9, 36608-36614. A new iCASE studentship was also funded starting in Sept 2020 on a new enzyme type. Another grant application has been submitted by Prof H Hailes (UCL) together with Almac. There are contracts that were signed (with Biochemical Engineering, UCL) with MTAs included and materials (enzymes) were transferred that are being used in commercial applications. Almac contributed £132k and an industrial perspective/time at attendance for meetings, etc.
Impact Publication in RSC Advances in 2019: D. Dobrijevic, L. Benhamou, A. E. Aliev, N. Dawson, D. Baud, D. Méndez Sánchez, N. Tappertzhofen, T. S. Moody, C. A. Orengo, H. C. Hailes, J. M. Ward, 'Ene-reductases from a drain metagenome for the selective bioreduction of bicyclic enones', RSC Adv., 2019, 9, 36608-36614.
Start Year 2017
 
Description Multienzyme Cascades Incorporating Methyltransferases for the Diversification of Alkaloids (Helen Hailes) 
Organisation University College London
Department Biochemical Engineering
Country United Kingdom 
Sector Academic/University 
PI Contribution Structural characterisation, chemical synthesis.
Collaborator Contribution Biochemical studies.
Impact Publications: DOI 10.1002/anie.202104476 The use of methyltransferases in vitro in multi-enzyme cascades, including for the generation of SAM in situ has been reported. Up to seven enzymes were used for the regioselective diversification of natural and non-natural THIQs on an enzymatic preparative scale. Regioselectivites of the methyltransferases were dependent on the group at C-1 and presence of fluorine in the THIQs. An interesting dual activity was also discovered for the catechol methyltransferases used, which were found to be able to regioselectively methylate two different catechols in a single molecule. The use of methyltransferases in vitro in multi-enzyme cascades, for the diversification of natural and non-natural THIQs was described. Regioselectivites of the methyltransferases were interestingly dependent on the group at C-1 and presence of fluorine in the THIQs. An interesting dual activity was also discovered for the catechol methyltransferases used, which were found to be able to regioselectively methylate two different catechols in a single molecule. DOI 10.1021/acs.orglett.1c02110 Chemoenzymatic cascades toward various 13-methyl-tetrahydroprotoberberbine scaffolds using a stereoselective Pictet-Spenglerase, regioselective catechol O-methyltransferases and selective chemical Pictet-Spengler reactions have been presented. All reactions could be performed sequentially, without the workup or purification of any synthetic intermediates. Moreover, the naturally occurring alkaloids have the (+)-configuration and importantly here, a strategy to the (-)-isomers was developed. A methyl group at C-8 was also introduced with some stereocontrol, influenced by the stereochemistry at C-13. Furthermore, a single step reaction was found to convert tetrahydroprotoberberine alkaloids into the analogous protoberberine scaffold, avoiding the use of harsh oxidizing conditions or a selective oxidase. This work provides facile, selective routes toward novel analogues of bioactive alkaloids. A novel cascades using norcoclaurine synthases to produce tetrahydroprotoberberine and protoberberine alkaloids were presented. DOI 10.1002/cctc.202101008 Transaminases were directly reacted with hydrazones in a novel approach to form amine products. Several substrates were investigated, including those with furan and phenyl moieties. It was determined that the amine yields increased when an additional electrophile was added to the reaction mixture, suggesting that they can sequester the hydrazine released in the reaction. Pyridoxal 5'-phosphate (PLP), a cofactor for transaminases, and polyethylene glycol (PEG)-aldehydes were both found to increase the yield of amine formed. Notably, the amination of (S)-1-amino-2-(methoxymethyl) pyrrolidine (SAMP) hydrazones gave promising results as a method to form chiral ß-substituted amines in good yield. A novel reaction using transaminases to convert hydrazones to amines was described.
Start Year 2018
 
Description Neuropilin-1 in vascular and immune biology (David Selwood). 
Organisation University College London
Department Institute of Structural and Molecular Biology
Country United Kingdom 
Sector Academic/University 
PI Contribution David Selwood: Working with Snezana Djordjevic (UCL ISMB) and Ian Zachary (UCL) and with Prof. Stella Tsirka (Stony Brook, USA) we helped to establish a role for neuropilin-1 in the immune system and in collaboration with Prof Tsirka we demonstrated the involvement of the TGFbeta pathway. We also demonstrated that blockade of neuropilin-1 could be an effective strategy against gliomas in mice. We obtained >£1m funding from biotech and developed effective small molecule inhibitors of this protein.
Collaborator Contribution Research
Impact Powell J, Mota F, Steadman D,.Selwood DL. Small Molecule Neuropilin-1 Antagonists Combine Antiangiogenic and Antitumor Activity with Immune Modulation through Reduction of Transforming Growth Factor Beta (TGFß) Production in Regulatory T-Cells. J Med Chem. 2018 May 10;61(9):4135-4154. The design, synthesis, and biological evaluation of some potent small-molecule neuropilin-1 (NRP1) antagonists have been reported. NRP1 is implicated in the immune response to tumors, particularly in Treg cell fragility, required for PD1 checkpoint blockade. The design of these compounds was based on a previously identified compound EG00229. The design of these molecules was informed and supported by X-ray crystal structures. Compound 1 (EG01377) was identified as having properties suitable for further investigation. Compound 1 was then tested in several in vitro assays and was shown to have antiangiogenic, antimigratory, and antitumor effects. Remarkably, 1 was shown to be selective for NRP1 over the closely related protein NRP2. In purified Nrp1+, FoxP3+, and CD25+ populations of Tregs from mice, 1 was able to block a glioma-conditioned medium-induced increase in TGFß production. This comprehensive characterization of a small-molecule NRP1 antagonist provides the basis for future in vivo studies. We showed that NRP1 antagonists could regulate the activity of Treg cells.
Start Year 2017
 
Description Noncovalent Interactions of p Systems with Sulfur 
Organisation University of Southampton
Department Chemistry
Country United Kingdom 
Sector Academic/University 
PI Contribution The relative strength of noncovalent interactions between a thioether sulfur atom and various p systems in designed top pan molecular balances was determined by NMR spectroscopy. Compared to its oxygen counterpart, the sulfur atom displays a remarkable ability to interact with almost equal facility over the entire range of p systems studied, with the simple alkene emerging as the most powerful partner. With the exception of the O···heteroarene interaction, all noncovalent interactions of sulfur with p systems are favoured over oxygen.
Collaborator Contribution Experimental structure determinations in the solid state were carried by our partners Dr. G.J.Tizzard and Prof. S. J. Coles from School of Chemistry, University of Southampton.
Impact Publication at http://onlinelibrary.wiley.com/wol1/doi/10.1002/an ie.201708485/abstract
Start Year 2017
 
Description Organic and Perovskite Solar Cells (Bob Schroeder, UCL) 
Organisation King Abdullah University of Science and Technology (KAUST)
Country Saudi Arabia 
Sector Academic/University 
PI Contribution A research collaboration, which has led to a recent publication in Chemistry of Materials, titled "A Nonionic Alcohol Soluble Polymer Cathode Interlayer Enables Efficient Organic and Perovskite Solar Cells" (DOI 10.1021/acs.chemmater.1c01430).
Collaborator Contribution Preparation of samples for structural characterisation. Interlayer materials were studied for organic solar cells.
Impact Publication DOI 10.1021/acs.chemmater.1c01430
Start Year 2020
 
Description Peptide ligation in water 
Organisation Simons Foundation
Country United States 
Sector Charity/Non Profit 
PI Contribution Amide bond formation is one of the most important reactions in both chemistry and biology. In 2007, the ACS Green Chemistry Institute voted 'amide formation avoiding poor atom economy reagents' as the top challenge for organic chemistry; this remains an unmet challenge. The universal genetic code establishes that the biological role of peptides predates Life's last universal common ancestor and that peptides played an essential role in the origins of life on Earth. Prof. M Powner (Chemistry, UCL) and his group have demonstrated the facile, selective and iterative coupling to a-aminonitriles in water to make peptide bonds. The unique reactivity of a-aminonitriles provides a direct link between the canonical peptide structures of biology and prebiotic synthesis. Traceless sulfide-mediated peptide ligation has been applied to the coupling reactions of all amino acid residues, with remarkably selective coupling in all cases. It was shown that the unique reactivity a-aminonitriles makes them singularly well-suited to (protecting-group-free) ligation at neutral pH.
Collaborator Contribution Simons Foundation has contributed £120k towards the 700MHz NMR facility used by Prof. M Powner (Chemistry, UCL) and his group in their research.
Impact Publication in Nature: Canavelli, P., Islam, S., Powner, M.W. Peptide ligation by chemoselective aminonitrile coupling in water. Nature, 571, 546-549 (2019). doi:10.1038/s41586-019-1371-4.
Start Year 2017
 
Description Peptide ligation in water (Matt Powner) 
Organisation Simons Foundation
Country United States 
Sector Charity/Non Profit 
PI Contribution Amide bond formation is one of the most important reactions in both chemistry and biology. In 2007, the ACS Green Chemistry Institute voted 'amide formation avoiding poor atom economy reagents' as the top challenge for organic chemistry; this remains an unmet challenge. The universal genetic code establishes that the biological role of peptides predates Life's last universal common ancestor and that peptides played an essential role in the origins of life on Earth. Prof. M Powner (Chemistry, UCL) and his group have demonstrated the facile, selective and iterative coupling to a-aminonitriles in water to make peptide bonds. The unique reactivity of a-aminonitriles provides a direct link between the canonical peptide structures of biology and prebiotic synthesis. Traceless sulfide-mediated peptide ligation has been applied to the coupling reactions of all amino acid residues, with remarkably selective coupling in all cases. It was shown that the unique reactivity a-aminonitriles makes them singularly well-suited to (protecting-group-free) ligation at neutral pH.
Collaborator Contribution Simons Foundation has contributed £120k towards the 700MHz NMR facility used by Prof. M Powner (Chemistry, UCL) and his group in their research.
Impact Publication in Nature: Canavelli, P., Islam, S., Powner, M.W. Peptide ligation by chemoselective aminonitrile coupling in water. Nature, 571, 546-549 (2019). doi:10.1038/s41586-019-1371-4.
Start Year 2017
 
Description Precursor design to develop new compounds for use in thin film growth 
Organisation Pilkington Glass
Country United Kingdom 
Sector Private 
PI Contribution Prof Claire Carmalt and Prof Ivan Parkin (Chemistry, UCL) are involved in investigating precursor design to develop new compounds for use in thin-film growth (Impact Acceleration Account award to UCL 2017-20, EP/R511638/1 and for grant EP/L017709)
Collaborator Contribution The partners provide research placements for our students and analysis of the thin films which we deposit. They are also involved in technical meetings with us and the students and provide advice on scale up. They are currently funding 4 EngD or PhD studentships and each studentship has a confidentiality agreement
Impact The UCL 700MHz NMR facility allowed for a detailed characterisation of a ZnO precursor and information of the structure of the compound formed.
Start Year 2017
 
Description Precursor design to develop new compounds for use in thin film growth (Carmalt and Parkin) 
Organisation Pilkington Glass
Country United Kingdom 
Sector Private 
PI Contribution Prof Claire Carmalt and Prof Ivan Parkin (Chemistry, UCL) are involved in investigating precursor design to develop new compounds for use in thin-film growth (Impact Acceleration Account award to UCL 2017-20, EP/R511638/1 and for grant EP/L017709)
Collaborator Contribution The partners provide research placements for our students and analysis of the thin films which we deposit. They are also involved in technical meetings with us and the students and provide advice on scale up. They are currently funding 4 EngD or PhD studentships and each studentship has a confidentiality agreement
Impact The UCL 700MHz NMR facility allowed for a detailed characterisation of a ZnO precursor and information of the structure of the compound formed.
Start Year 2017
 
Description Prof Frances Brodski 
Organisation University College London
Department Division of Biosciences
Country United Kingdom 
Sector Academic/University 
PI Contribution Clathrin protein and conformational studies in solution
Collaborator Contribution Prof Brodski's team contributed to the project by providing, preparing and characterising the samples that were imaged by our team via liquid TEM
Impact Not yet, experiments were interrupted by COVID.
Start Year 2020
 
Description Prof Francesco Stellaci 
Organisation Swiss Federal Institute of Technology in Lausanne (EPFL)
Country Switzerland 
Sector Public 
PI Contribution Herpes 2 virus: structure , assembly and interaction with NPs via Liquid TEM
Collaborator Contribution Herpes 2 virus: structure , assembly and interaction with NPs via Liquid TEM
Impact Not yet
Start Year 2020
 
Description Tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass 
Organisation GlaxoSmithKline (GSK)
Country Global 
Sector Private 
PI Contribution Professor Helen Hailes (Department of Chemistry, UCL), Professor Tom Sheppard (Department of Chemistry, UCL), Dr Gary Lye (Biochemical Engineering, UCL) and Dr Christopher J. Tame (GSK) are involved in this collaboration. For details, see the following publication: L. Benhamou, R. W. Foster, D. P. Ward, K. Wheelhouse, L. Sloan, C. J. Tame, D.-K. Bucar, G. J. Lye, H. C. Hailes, T. D. Sheppard, 'Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass', Green Chem., 2019, 21, 2035-2042. For this publication, the facility was invaluable in characterizing the products generated from biomass-derived starting materials. Selective dehydrations of pentose sugars were achieved under basic or acidic conditions, and the equipment allowed NMR reaction monitoring and the ability to distinguish between the isomeric products formed. Fragments for medicinal chemistry applications containing primary alcohol, ketone, carboxylic acid or amine functional groups were generated, suitable for incorporation into fragment/lead libraries. Funding EPSRC (EP/K503745/1) and building upon outputs from EP/K014897.
Collaborator Contribution GSK and AstraZeneca have added the samples of the chiral fragments prepared by Professor Helen Hailes (Department of Chemistry, UCL), Professor Tom Sheppard (Department of Chemistry, UCL) and Dr Gary Lye (Biochemical Engineering, UCL) for use in their fragment libraries. For further details, see the following publication: L. Benhamou, R. W. Foster, D. P. Ward, K. Wheelhouse, L. Sloan, C. J. Tame, D.-K. Bucar, G. J. Lye, H. C. Hailes, T. D. Sheppard, 'Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass', Green Chem., 2019, 21, 2035-2042.
Impact Joint publication in Green Chemistry: L. Benhamou, R. W. Foster, D. P. Ward, K. Wheelhouse, L. Sloan, C. J. Tame, D.-K. Bucar, G. J. Lye, H. C. Hailes, T. D. Sheppard, 'Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass', Green Chem., 2019, 21, 2035-2042.
Start Year 2017
 
Description Tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass (Helen Hailes) 
Organisation GlaxoSmithKline (GSK)
Country Global 
Sector Private 
PI Contribution Professor Helen Hailes (Department of Chemistry, UCL), Professor Tom Sheppard (Department of Chemistry, UCL), Dr Gary Lye (Biochemical Engineering, UCL) and Dr Christopher J. Tame (GSK) are involved in this collaboration. For details, see the following publication: L. Benhamou, R. W. Foster, D. P. Ward, K. Wheelhouse, L. Sloan, C. J. Tame, D.-K. Bucar, G. J. Lye, H. C. Hailes, T. D. Sheppard, 'Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass', Green Chem., 2019, 21, 2035-2042. For this publication, the facility was invaluable in characterizing the products generated from biomass-derived starting materials. Selective dehydrations of pentose sugars were achieved under basic or acidic conditions, and the equipment allowed NMR reaction monitoring and the ability to distinguish between the isomeric products formed. Fragments for medicinal chemistry applications containing primary alcohol, ketone, carboxylic acid or amine functional groups were generated, suitable for incorporation into fragment/lead libraries. Funding EPSRC (EP/K503745/1) and building upon outputs from EP/K014897.
Collaborator Contribution GSK and AstraZeneca have added the samples of the chiral fragments prepared by Professor Helen Hailes (Department of Chemistry, UCL), Professor Tom Sheppard (Department of Chemistry, UCL) and Dr Gary Lye (Biochemical Engineering, UCL) for use in their fragment libraries. For further details, see the following publication: L. Benhamou, R. W. Foster, D. P. Ward, K. Wheelhouse, L. Sloan, C. J. Tame, D.-K. Bucar, G. J. Lye, H. C. Hailes, T. D. Sheppard, 'Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass', Green Chem., 2019, 21, 2035-2042.
Impact Joint publication in Green Chemistry: L. Benhamou, R. W. Foster, D. P. Ward, K. Wheelhouse, L. Sloan, C. J. Tame, D.-K. Bucar, G. J. Lye, H. C. Hailes, T. D. Sheppard, 'Functionalised tetrahydrofuran fragments from carbohydrates or sugar beet pulp biomass', Green Chem., 2019, 21, 2035-2042.
Start Year 2017
 
Description Tin chemical shift anisotropy in tin dioxide 
Organisation Rutherford Appleton Laboratory
Department Scientific Computing Department
Country United Kingdom 
Sector Public 
PI Contribution Experimental NMR measurements of 119Sn and 31P NMR powder lineshapes using 300 MHz and 700 MHz NMR facilities.
Collaborator Contribution Computational predictions of NMR chemical shift anisotropy
Impact Publication at https://www.sciencedirect.com/science/article/pii/S0926204017301303?via=ihub#!
Start Year 2017
 
Description Tin chemical shift anisotropy in tin dioxide 
Organisation University of Oxford
Country United Kingdom 
Sector Academic/University 
PI Contribution Experimental NMR measurements of 119Sn and 31P NMR powder lineshapes using 300 MHz and 700 MHz NMR facilities.
Collaborator Contribution Computational predictions of NMR chemical shift anisotropy
Impact Publication at https://www.sciencedirect.com/science/article/pii/S0926204017301303?via=ihub#!
Start Year 2017
 
Description collaboration with Lennon Group From Glasgow university 
Organisation University of Glasgow
Department Institute of Infection, Immunity and Inflammation
Country United Kingdom 
Sector Academic/University 
PI Contribution Hosting mentoring and consulting on the projects of two CASE Students from Glasgow who are seconded to Harwell with the Catalysis Hub. Providing access to Catalysis hub analysis and testing equipment
Collaborator Contribution Aligning two case Students with the Hub research portfolio and ethos.
Impact ongoing leading to two PHDs
Start Year 2016
 
Description "Assessing dynamics of Soft Matter and Biological systems in liquid state", Microscopy Society of Ireland Symposium, 6th and 7th January 2021, virtual conference. 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact http://symposia.microscopy.ie
Year(s) Of Engagement Activity 2021
 
Description 2 talks atXAFS 2015 Karlsruhe, Germany, September 2015 - oral presentation 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Other audiences
Results and Impact 2 taks on XAFS and XAFS/Drifts at the confernce
Year(s) Of Engagement Activity 2015
 
Description A visit and spectra for The King Fahad Academy Bromyard Avenue London 
Form Of Engagement Activity Participation in an open day or visit at my research institution
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Schools
Results and Impact A visit took place on 31 October 2017, during which the NMR equipment including the new 700 MHz NMR was demonstrated. This was followed by measurements of NMR spectra for the student projects (Extended Essay in Chemistry).
Year(s) Of Engagement Activity 2017
 
Description EPRSC/Jeol Centre for Liquid Phase Electron Microscopy (LPEM) on Liquid Phase Electron Microscopy 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact Organised the first workshop at the EPRSC/Jeol Centre for Liquid Phase Electron Microscopy (LPEM) on Liquid Phase Electron Microscopy (November 2019) in partnership with DENSsolution and Quantum Design UK. The intention is to run this workshop on an annual basis.
The workshop was very well received and was attended by Industry as well as academic representatives.
Year(s) Of Engagement Activity 2019
 
Description Evidence on Quantum Technologies to the Science and Technology Committee of the House of Commons 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Policymakers/politicians
Results and Impact Evidence to MPs would be part of an overall effort in justifying present and future funding of this area of science.
Year(s) Of Engagement Activity 2018
 
Description Leading a Faraday Discussion on Catalysis organised by the RSC April 2016 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Other audiences
Results and Impact Designing New Heterogeneous Catalysts: Faraday Discussion
4 - 6 April 2016, London, United Kingdom
Catalysis is a core area of contemporary science posing major fundamental and conceptual challenges, while being at the heart of the chemical industry. It is a major theme in chemical sciences and engineering that underlies much of the key research and teaching in these subjects.
At this discussion, we will bring the catalysis community together to discuss the theme of designing new heterogeneous catalysts. Catalysis plays a crucial part in the production of 80% of all manufactured goods. We will explore the modern methods used to design new catalysts and how the approaches can bridge across the disciplines of physical sciences and chemical engineering
Themes
Catalyst design from theory to practice
In this session, we will explore how modern theoretical methods are aiding the design of new heterogeneous catalysts. This will invariably provide interplay between mechanism and the active site
Designing new catalysts: synthesis of new active structures
In this session, we will discuss ways in which new nanoparticulate structures can play a role in designing new active centres. How they can be prepared and their catalytic properties explored
Bridging model and real catalysts
We will discuss how modern methods in surface science and microscopy can aid the design of new catalysts. Recent advances in methodologies are enabling model surface science studies and real catalysts come closer together. This session will explore the nature of active catalyst sites
Application of novel catalysts
In this session we aim to show how new catalyst designs can find important applications that address key challenges facing society at this time, such as energy and water purification
Year(s) Of Engagement Activity 2016
URL http://www.rsc.org/events/detail/16840/designing-new-heterogeneous-catalysts-faraday-discussion
 
Description NMR visits for schools 
Form Of Engagement Activity Participation in an open day or visit at my research institution
Part Of Official Scheme? No
Geographic Reach Regional
Primary Audience Schools
Results and Impact The new equipment was demonstrated to school pupils visiting UCL Chemistry on the Spectroscopy Day in September 2017 and in April 2018.
Year(s) Of Engagement Activity 2017,2018,2019
URL https://www.ucl.ac.uk/chemistry/schools/schools-programme
 
Description Oral presentation and poster at Operando V, Deauville, France May 2015 - poster 
Form Of Engagement Activity A talk or presentation
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Other audiences
Results and Impact E gibson )Catalysis Hub) and P Wells (Catalysis at Harwell) gave excellent talks on techniques developed by the hub and the centre at Harwell
Year(s) Of Engagement Activity 2015
 
Description Organiation and participation of a Royal society Discussion meeting Catalysis improving society 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Other audiences
Results and Impact The successful operation of catalysis lies at the heart of the wellbeing of society and this meeting will address modern developments in designing improved catalysts especially in non traditional application areas such as water purification. We will bring together scientists across the breadth of catalysis (heterogeneous, homogeneous and bio) bridging the expertise of chemists, engineers, bio-scientists and theoreticians.
Year(s) Of Engagement Activity 2015
URL https://royalsociety.org/science-events-and-lectures/2015/06/catalysis-dm/
 
Description Provision of NMR service to users from Industry and Academia 
Form Of Engagement Activity Participation in an open day or visit at my research institution
Part Of Official Scheme? No
Geographic Reach Regional
Primary Audience Postgraduate students
Results and Impact Users from other UCL departments and other UK universities visited the facility. Spectra were recorded on the new facility for users from other universities, as well as from industrial companies.
Year(s) Of Engagement Activity 2017,2018,2019,2020
 
Description Provision of NMR service to users from Industry and Academia 
Form Of Engagement Activity Participation in an open day or visit at my research institution
Part Of Official Scheme? No
Geographic Reach Regional
Primary Audience Postgraduate students
Results and Impact Users from other UCL departments and other UK universities visited the facility. Spectra were recorded on the new facility for users from other universities, as well as from industrial companies. We have run NMR spectra for such companies as Abcam Plc (Cambridge), Byotrol, Darr House, Gurit, Key Organics. Researchers from Birkbeck College and Westminster University, as well as from various UCL departments, including Dementia Research Centre, Chemical Engineering, Eastman Dental Institute, Royal Free Hospital, have used the facility on the regular basis.
Year(s) Of Engagement Activity 2017,2018,2019,2020,2021,2022
 
Description ROyal Society Summer Science Exhibition - Zoom for improvement 2017 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Public/other audiences
Results and Impact Royal society summer sicience exhibition - Zoom for improvement Catalysis is everywhere - it makes chemical reactions more efficient and faster, so we can produce more products that we need for a cheaper price. The fuel in your car has been made from crude oil, using a series of catalytic reactions to allow the fuel to flow and burn correctly, delivering energy to your car. The gases produced are processed in the car's catalytic converter which uses catalysis to transform polluting carbon and nitrogen oxides that are the result of burning the fuel into environmentally benign compounds. Over 80% of the nitrogen in the proteins in your body has been derived from fertilizers produced using catalysis.

We are working in the 'Green Chemistry' research field, working to realise a sustainable future for the world. We want to understand catalysis and the materials we use to produce everyday goods and energy - and to produce fuels and other chemicals using renewable resources from plant material. We want to move to a more sustainable economy where the things we use and the energy we need is produced in a renewable way.

Because catalysis is a molecule by molecule process, we need to understand how it works and study materials at the level of individual atoms using very powerful 'electron microscopes'. We also use very high energy light to look at catalysts at this scale while they are working, to understand and improve catalyst materials. We are recreating industrial conditions in the lab and are working out what makes a good or bad catalyst. We have discovered that the most promising catalysts are solids containing molecules called nanoparticles.

Our research is revealing more about catalysis and how it can help us move towards a more sustainable future
Year(s) Of Engagement Activity 2017
URL https://royalsociety.org/science-events-and-lectures/2017/summer-science-exhibition/exhibits/zoom-fo...
 
Description Spotlight on drifts 
Form Of Engagement Activity A magazine, newsletter or online publication
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Postgraduate students
Results and Impact this is an informative piece and lead to more use of the machine
Year(s) Of Engagement Activity 2018
URL https://www.ses.ac.uk/2017/09/27/drifts-spectrometer/
 
Description Student groups - Quantum Technologies 
Form Of Engagement Activity A formal working group, expert panel or dialogue
Part Of Official Scheme? No
Geographic Reach Local
Primary Audience Other audiences
Results and Impact Increased interest in Quantum Technology among students
Year(s) Of Engagement Activity 2013,2017
 
Description UK Catalysis Hub Conferences 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach National
Primary Audience Other audiences
Results and Impact The Catalysis Hub runs two conferences per year for members of the Hub and for the wider catalysis community. These conferences showcase catalysis research focusing on the work of the Hub. Speakers include researchers from the Catalysis Hub and internationally renowned speakers and industrialists who cover a range of topics including biocatalysis, homogeneuos and heterogeneous catalysis, reaction engineering and industrial catalysis. In addition, poster sessions highlights the projects across the Hub and provide a lively forum for discussion and dissemination of catalytic science.
One aim of the UK Catalysis Hub is to develop the next generation of researchers. To facilitate this aim, the UK Catalysis Hub arranges an annual summer conference focusing on providing a forum for the research associates to present their work and interact. Attendance at the conferences is consistently over 100 people. Dinner speakers have included EPSRC, international academics and industrialists
Year(s) Of Engagement Activity 2013,2014,2015,2016,2017
 
Description Webminar Nanotalks , presentation title "4D Liquid Phase TEM or Soft Organic Materials" on 7th (Europe and Asia) and 9th (America) July 2020 
Form Of Engagement Activity Participation in an activity, workshop or similar
Part Of Official Scheme? No
Geographic Reach International
Primary Audience Professional Practitioners
Results and Impact Webminar was recorded here : https://www.youtube.com/watch?v=2k7K50F3Je0, 288 views.
Year(s) Of Engagement Activity 2020