Properties and applications of Janus faced fluorocyclohexanes
Lead Research Organisation:
University of St Andrews
Department Name: Chemistry
Abstract
This research proposal has its origin in the special properties of the selectively fluorinated molecule, all-cis-1,2,3,4,5,6-hexafluorocyclohexane, which we prepared and reported in 2015. This is cyclohexane ring system which emerges as the most polar aliphatic compound recorded and it has interesting properties such as the ability to associate with both cations and anions. The cyclohexane ring is highly unusual in that it has polarised faces. The fluorine face is negatively polarised and the hydrogen face is positively polarised. In 2015 this ring system was challenging to make, and particularly to make derivatives, however in 2017 a direct hydrogenation method was developed by Glorius's lab in Munster, which allows access to derivatived forms of the ring system directly from aromatic precursors. Relevant to this proposal will be the synthesis of a series of substituted pentafluorocyclohexanes, where all substituents are on the same side of the cyclohexane ring. With this development, this research programme aims to explore applications of these pentafluorocyclohexane ring systems, exploring properties relevant to medicinal and biological chemistry (interactions with amino acids and proteins) as well as in organic materials and we have selected a particular focus in the areas of liquid crystals.
In the context of medicinal and biological chmeistry we want to explore how these ring systems will be expected to interact and bind with proteins. The negatively and positively polarised faces have the potential to make interactions with amino acid side chains with a complementary electrostatic profile. This will be explored by tagged 'pull-down' assays and proteins of high affinity will be identified by proteomics techniques. Candidate proteins will be progressed to co-crytsalisation structural (X-ray) studies for close structural analysis. In a complementary approach we will prepare tripeptides, from amino acid combinations that are known to be predisposed towards crystallinity. We will prepare a range of these with an amino acid with an all cis-2,3,4,5,6-pentafluorocyclohexyl side chain to explore how it interacts with other amino acid side chains. This study will extend to exploring the binding of this ring system to viral proteases, by making appropriate changes to drug molecules by replacing cyclohexyl or fluoroaromatic rings with the all cis-2,3,4,5,6-pentafluorocyclohexyl side chain. Structural biology(X-ray) analysis will allow us to determine how these ring systems interact with the protein, and this will inform medicinal chemists as to the potential of this motif.
The programme will extend to CF3 containing cyclohexanes, but particulary rings with more than one CF3 and with a defined stereochemistry. We have recently demonstrated that cyclohexanes with multiple CF3 groups attached to the aliphatic ring can also be accessed efficiently by the direct hydrogenation of arylCF3 precursors. The programme will extend to exploring the preparation, properties and chemistry of cyclohexanes with two and three CF3 groups with defined stereochemistries. These are also highly polarised aliphatics and these novel motifs will be introduced into liquid crystal architectures to exemplify properties and potential. The liquid crystal aspect is supported by Merck Liquid Crystal Division in Darmstadt who will carry out detailed analysis of prpared materials.
In overview the programme will explore an exciting class of organic chemistry motif which have potential to contribute new properties in a range of discovery chemistry arenas.
In the context of medicinal and biological chmeistry we want to explore how these ring systems will be expected to interact and bind with proteins. The negatively and positively polarised faces have the potential to make interactions with amino acid side chains with a complementary electrostatic profile. This will be explored by tagged 'pull-down' assays and proteins of high affinity will be identified by proteomics techniques. Candidate proteins will be progressed to co-crytsalisation structural (X-ray) studies for close structural analysis. In a complementary approach we will prepare tripeptides, from amino acid combinations that are known to be predisposed towards crystallinity. We will prepare a range of these with an amino acid with an all cis-2,3,4,5,6-pentafluorocyclohexyl side chain to explore how it interacts with other amino acid side chains. This study will extend to exploring the binding of this ring system to viral proteases, by making appropriate changes to drug molecules by replacing cyclohexyl or fluoroaromatic rings with the all cis-2,3,4,5,6-pentafluorocyclohexyl side chain. Structural biology(X-ray) analysis will allow us to determine how these ring systems interact with the protein, and this will inform medicinal chemists as to the potential of this motif.
The programme will extend to CF3 containing cyclohexanes, but particulary rings with more than one CF3 and with a defined stereochemistry. We have recently demonstrated that cyclohexanes with multiple CF3 groups attached to the aliphatic ring can also be accessed efficiently by the direct hydrogenation of arylCF3 precursors. The programme will extend to exploring the preparation, properties and chemistry of cyclohexanes with two and three CF3 groups with defined stereochemistries. These are also highly polarised aliphatics and these novel motifs will be introduced into liquid crystal architectures to exemplify properties and potential. The liquid crystal aspect is supported by Merck Liquid Crystal Division in Darmstadt who will carry out detailed analysis of prpared materials.
In overview the programme will explore an exciting class of organic chemistry motif which have potential to contribute new properties in a range of discovery chemistry arenas.
Planned Impact
Who will benefit from this research?
Organofluorine compounds make up 20% of all pharmaceuticals products internationally and 30% or all agrochemical products on the market. The organic materials industry relies very heavily on selectively fluorinated organic compounds and polymers. So innovation in the selective incorporation of fluorine contributes substantially to products that are designed to improve health, well being and the societal challenges of a growing population and a rapidy developing third world sector (BRIC Nations). That is the global perspective of who will benefit from this research. More tangibly this research programme is focussed on the medicinal and agrochemicals sectors and also on the organic materials industry (liquid crystals for displays).
Innovative thinking and the demonstration of new properties of organic compounds also impacts significantly on researchers within Univeristies including both experimentalists and theorists. New methods of synthesis and an exploration of the properties of organic fluorine compounds continue to attract attention in fundamental research environemnts, and there has been a notable increase in research activity in organic fluorine chemistry in publically funded institutes over the last decade.
How will they benefit?
Companies involved in the discovery of new bioactive organic molecules will benefit by being able to utilise these new motifs in their own research programmes. They will hopefully be stimuated by their unique properties and researchers in the area will be able to appliy or modify to their own purposes. Therefore the programme will stimulate thinking, and new approaches to current problems and challenges in drug and agrochemical discovery as well as in organic materials.
The St Andrews lab has a continual ongoing dialogue (conferences, lectures, hosting visitors, collaborations) with relevant individuals in the chemical industry, who have interests in the chemistry, properties and performance of fluorine.
The PDRAs will develop synthesis skills and know how in organic fluorine chemistry and they will become specialists in understanding the specific effects of fluorine in terms of modulating properties (Dial a molecule; Grand Challenge).
St Andrews University is proactive in developing IP. This will be developed in consultation with Business Development Managers (BDMs) associated with Research Business Development & Contracts.
Beneficiaries within the wider public? Results from such a programme will be used in more general arenas for discussing the relevance of chemistry and molecular design behaviour and performance in the service of food security, health and communications (LC displays). This type of programme is particularly well suited to public interactions because it engages with these major societal concerns.
The research will be published and disseminated enthusiastically in leading journals and at appropriate international conferences.
Organofluorine compounds make up 20% of all pharmaceuticals products internationally and 30% or all agrochemical products on the market. The organic materials industry relies very heavily on selectively fluorinated organic compounds and polymers. So innovation in the selective incorporation of fluorine contributes substantially to products that are designed to improve health, well being and the societal challenges of a growing population and a rapidy developing third world sector (BRIC Nations). That is the global perspective of who will benefit from this research. More tangibly this research programme is focussed on the medicinal and agrochemicals sectors and also on the organic materials industry (liquid crystals for displays).
Innovative thinking and the demonstration of new properties of organic compounds also impacts significantly on researchers within Univeristies including both experimentalists and theorists. New methods of synthesis and an exploration of the properties of organic fluorine compounds continue to attract attention in fundamental research environemnts, and there has been a notable increase in research activity in organic fluorine chemistry in publically funded institutes over the last decade.
How will they benefit?
Companies involved in the discovery of new bioactive organic molecules will benefit by being able to utilise these new motifs in their own research programmes. They will hopefully be stimuated by their unique properties and researchers in the area will be able to appliy or modify to their own purposes. Therefore the programme will stimulate thinking, and new approaches to current problems and challenges in drug and agrochemical discovery as well as in organic materials.
The St Andrews lab has a continual ongoing dialogue (conferences, lectures, hosting visitors, collaborations) with relevant individuals in the chemical industry, who have interests in the chemistry, properties and performance of fluorine.
The PDRAs will develop synthesis skills and know how in organic fluorine chemistry and they will become specialists in understanding the specific effects of fluorine in terms of modulating properties (Dial a molecule; Grand Challenge).
St Andrews University is proactive in developing IP. This will be developed in consultation with Business Development Managers (BDMs) associated with Research Business Development & Contracts.
Beneficiaries within the wider public? Results from such a programme will be used in more general arenas for discussing the relevance of chemistry and molecular design behaviour and performance in the service of food security, health and communications (LC displays). This type of programme is particularly well suited to public interactions because it engages with these major societal concerns.
The research will be published and disseminated enthusiastically in leading journals and at appropriate international conferences.
People |
ORCID iD |
David O'Hagan (Principal Investigator) |
Publications
Clark JL
(2021)
Janus All-Cis 2,3,4,5,6-Pentafluorocyclohexyl Building Blocks Applied to Medicinal Chemistry and Bioactives Discovery Chemistry.
in Chemistry (Weinheim an der Bergstrasse, Germany)
Clark JL
(2021)
Supramolecular packing of alkyl substituted Janus face all-cis 2,3,4,5,6-pentafluorocyclohexyl motifs.
in Chemical science
Dobson LS
(2023)
Aryl (ß,ß',ß?-Trifluoro)-tert-butyl: A Candidate Motif for the Discovery of Bioactives.
in Organic letters
Fang Z
(2023)
Does Perdeuteration Increase the Polarity of Janus Face Cycloalkanes?
in Helvetica Chimica Acta
Fang Z
(2020)
Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes.
in Beilstein journal of organic chemistry
Fischer C
(2023)
Lateral dipole moments induced by all-cis-pentafluorocyclohexyl groups cause unanticipated effects in self-assembled monolayers
in Nano Research
O'Hagan D
(2023)
The Emergence and Properties of Selectively Fluorinated 'Janus' Cyclohexanes.
in Chemical record (New York, N.Y.)
Piscelli BA
(2020)
Fluorine-Induced Pseudo-Anomeric Effects in Methoxycyclohexanes through Electrostatic 1,3-Diaxial Interactions.
in Chemistry (Weinheim an der Bergstrasse, Germany)
Piscelli BA
(2021)
The contribution of non-classical CHaxOC hydrogen bonds to the anomeric effect in fluoro and oxa-methoxycyclohexanes.
in Physical chemistry chemical physics : PCCP
Poskin TJ
(2022)
Janus faced fluorocyclohexanes for supramolecular assembly: synthesis and solid state structures of equatorial mono-, di- and tri alkylated cyclohexanes and with tri-axial C-F bonds to impart polarity.
in Chemical communications (Cambridge, England)
Description | This research elaborated extensively on the nature of selectively fluorinated cyclohexane rings. It has resulted in other groups in academia and industry publishing papers associated with these materials. Eg Genentech In California published their own assessment of these ring motifs for medicinal chemistry; see Turning the Other Cheek: Influence of the cis-Tetrafluorocyclohexyl Motif on Physicochemical and Metabolic Properties Yong Wang, Wendy Lee, Yi-Chen Chen, Yuhui Zhou, Emile Plise, Madyson Migliozzi, and James J. Crawford, ACS Med. Chem. Lett. 2022, 13, 9, 1517-1523. We are collaborating with a group in Japan Prof Shigeuki Yamada at Kyoto Inst technology, and a group in germany Prof Peer Kirsch, University of Darmstadt, on the performance of thesis molecules as liquid crystals and as memory storage materials respectively. |
Exploitation Route | We have an application submitted to EPSR on incorporating these molecules into MOFs. This is also to fund acollaboration with a research group in Brazil at the University of Campinas, exploring the properties of these fluorinated cyclohexanes as organic materials. |
Sectors | Chemicals Healthcare Pharmaceuticals and Medical Biotechnology |
Description | A major phara company (Genetec Ltd) have explored our Janus face motifs and provided further comentary on their utility in medchem...see key paper below Yong Wang, Wendy Lee, Yi-Chen Chen, Yuhui Zhou, Emile Plise, Madyson Migliozzi, and James J. Crawford ACS Medicinal Chemistry Letters 2022 13 (9), 1517-1523 DOI: 10.1021/acsmedchemlett.2c00312 |
First Year Of Impact | 2022 |
Sector | Healthcare |
Impact Types | Societal |
Title | CCDC 2068702: Experimental Crystal Structure Determination |
Description | Related Article: Joshua L. Clark, Alaric Taylor, Ailsa Geddis, Rifahath M. Neyyappadath, Bruno A. Piscelli, Cihang Yu, David B. Cordes, Alexandra M. Z. Slawin, Rodrigo A. Cormanich, Stefan Guldin, David O'Hagan|2021|Chemical Science|12|9712|doi:10.1039/D1SC02130C |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc27fnbp&sid=DataCite |
Title | CCDC 2068703: Experimental Crystal Structure Determination |
Description | Related Article: Joshua L. Clark, Alaric Taylor, Ailsa Geddis, Rifahath M. Neyyappadath, Bruno A. Piscelli, Cihang Yu, David B. Cordes, Alexandra M. Z. Slawin, Rodrigo A. Cormanich, Stefan Guldin, David O'Hagan|2021|Chemical Science|12|9712|doi:10.1039/D1SC02130C |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc27fncq&sid=DataCite |
Title | CCDC 2068704: Experimental Crystal Structure Determination |
Description | Related Article: Joshua L. Clark, Alaric Taylor, Ailsa Geddis, Rifahath M. Neyyappadath, Bruno A. Piscelli, Cihang Yu, David B. Cordes, Alexandra M. Z. Slawin, Rodrigo A. Cormanich, Stefan Guldin, David O'Hagan|2021|Chemical Science|12|9712|doi:10.1039/D1SC02130C |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc27fndr&sid=DataCite |
Title | CCDC 2068705: Experimental Crystal Structure Determination |
Description | Related Article: Joshua L. Clark, Alaric Taylor, Ailsa Geddis, Rifahath M. Neyyappadath, Bruno A. Piscelli, Cihang Yu, David B. Cordes, Alexandra M. Z. Slawin, Rodrigo A. Cormanich, Stefan Guldin, David O'Hagan|2021|Chemical Science|12|9712|doi:10.1039/D1SC02130C |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc27fnfs&sid=DataCite |
Title | CCDC 2068706: Experimental Crystal Structure Determination |
Description | Related Article: Joshua L. Clark, Alaric Taylor, Ailsa Geddis, Rifahath M. Neyyappadath, Bruno A. Piscelli, Cihang Yu, David B. Cordes, Alexandra M. Z. Slawin, Rodrigo A. Cormanich, Stefan Guldin, David O'Hagan|2021|Chemical Science|12|9712|doi:10.1039/D1SC02130C |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc27fngt&sid=DataCite |
Title | CCDC 2068707: Experimental Crystal Structure Determination |
Description | Related Article: Joshua L. Clark, Alaric Taylor, Ailsa Geddis, Rifahath M. Neyyappadath, Bruno A. Piscelli, Cihang Yu, David B. Cordes, Alexandra M. Z. Slawin, Rodrigo A. Cormanich, Stefan Guldin, David O'Hagan|2021|Chemical Science|12|9712|doi:10.1039/D1SC02130C |
Type Of Material | Database/Collection of data |
Year Produced | 2021 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc27fnhv&sid=DataCite |
Title | CCDC 2270745: Experimental Crystal Structure Determination |
Description | Related Article: Luca S. Dobson, Qingzhi Zhang, Benjamin A. McKay, Oluwayinka Oke, Chukwuemeka Isanbor, Mohd Faheem Khan, Bruno A. Piscelli, David B. Cordes, Rodrigo A. Cormanich, Cormac D. Murphy, David O'Hagan|2023|Org.Lett.|||doi:10.1021/acs.orglett.3c02236 |
Type Of Material | Database/Collection of data |
Year Produced | 2023 |
Provided To Others? | Yes |
URL | http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/ccdc.csd.cc2g6wvf&sid=DataCite |
Description | Liquid crystal analysis Kyoto Japan |
Organisation | Kyoto Institute of Technology |
Country | Japan |
Sector | Academic/University |
PI Contribution | We have made a range of fluorinated motifs by organic synthesis, and assembled thm into liquid crystal type molecules, used in vertical alignment displays. |
Collaborator Contribution | They have made differential scanning calorimetric (DSC) measurements and polarising optical microscope measurements (POM) to determine the nature and properties of the materilas at different phase transitions relevant to characterising liquid crystal materials |
Impact | Shigeyuki Yamada, Masato Morita, Yizhou Wang, Qingzhi Zhang, David O'Hagan, Tomohiro Agou, Hiroki Fukumoto, Toshio Kubota, Mitsuo Hara. Tsutomu Konno Effect of fluoroalkyl-substituent in bistolane-based photoluminescence liquid crystals on their physical behaviour. Crystals, 2021, 11, 450. |
Start Year | 2019 |