A New Iron Age: Atom efficient P-C bond forming reactions with simple, designed iron catalysts

Lead Research Organisation: University of Bath
Department Name: Chemistry

Abstract

Catalysis is the process by which chemical reactions are made to run faster at lower temperature. The vast majority of chemical industries rely on developing catalysis therefore making vital industrial processes, fundamental to the pharmaceutical, agrochemical and fine chemical industries, easier and more cost efficient. Catalysis allows us to precisely modify chemical structure through the ability to make and break specific chemical bonds. Catalyst design is therefore an incredibly important and vital undertaking: the key to unlocking new reactivity and new bond forming methods.

This project looks into the design of catalysts which contain staggeringly simple motifs along with abundant and inexpensive iron centre. Iron is also biocompatible and non-toxic providing a strong foundation for our targeted reaction: hydrophosphination. These reactions allow the synthesis of carbon-phosphorus bonds using efficient reaction conditions, forming key motifs or new architectures with ease. The preparation of phosphorus-containing motifs cannot be underestimated, allowing the preparation of new ligands, organocatalysts and biologically relevant motifs vital to a host of crucial manufacturing sectors. Beyond this we will develop this carbon-phosphorus bond forming chemistry for the preparation of new building blocks to construct non-burning plastics (high value materials used in advanced electronic devices and as commodity chemicals in the flame retardants industries).

The aim:
* Investigate their potential in 100% atom-economic processes which make molecules relevant to the pharmaceutical and agrochemical industries.
* Generate high value chemicals by developing a new route to the building blocks for phosphorus-containing plastics; this new route gives access to new plastics.

Planned Impact

Society:
In the medium to long term society will benefit from this research because it is envisaged that the development of new ligands will allow more efficient syntheses of important organic motifs (lower loading of pre-catalyst, lower reaction temperature means reduced production cost of chemicals). Catalyst design gives us the potential to undertake new reactions, generate new motifs or make and break bonds that have never been achieved before. This has the potential to open up new avenues in molecular space, the importance of this lies firmly in the pharmaceutical/ agrochemicals sector where the drug pipeline has started to dry up due to limitations on the areas of chemical space that can be accessed through standard synthetic transformations: new drug molecules means better healthcare.

The focus of this research is on simple ligands complexed to iron: if we can start to undertake industrially important synthesis of phosphorus-containing molecules in such a way, replacing the need for the use of the Platinum Group Metals (PGMs), then these expensive and rare metals can be used for other applications were there are currently no alternatives. As a result the development of new processes which utilise an alternative to the PGMs is of fundamental importance. Therefore the overarching impact from these outcomes will also be economic: cleaner, greener, cheaper syntheses along with new drug molecules.

A new route to phosphaalkenes would allow the development of new phosphorus-containing polymers. With access to new materials we envisage new or improved properties/ applications, benefiting industry and thus society as a whole.


People:
The PDRA will become highly trained in all aspects of synthetic inorganic chemistry, organic chemistry and polymer science, leaving them well-positioned to continue to pursue a career in academia or industry. The impact activities incorporated into the proposal will also leave the PDRA with a strong network in industry and with softer skills related to public engagement and the promotion of synthetic chemistry, thus having a positive impact on society.


Business:
In addition to the collaborators, this research will impact upon the wider chemical industries, most notably pharmaceutical, biomedical, agrochemical and fine chemicals manufacturers. Presentation of our research at the CatScI industry conference (Spring 2016) as well as hosting an open forum session at the conference will help to engage attendees from industry (in the past this has included Astra Zeneca, Bayer CropScience, Chiral Quest, Dr Reddy's Laboratories Inc., EcoSynth, Jansene Pharmaceutica, Johnson Matthey, PhosphonicS to name but a few) and help influence future research plans. Industry will benefit from first-hand experience of accessible, tuneable, inexpensive catalysts derived from simple precursors and an abundant metal. Abundant metal catalysis is gathering momentum in academia, but the uptake within industry lags behind: presenting research at leading industry conferences will help to deliver high impact science to its key market.

Malonic acid (one of our ligand precursors), although useful in biological treatments, has limited use in synthetic chemistry. Malonic acid can be prepared from the fermentation of biomass and either hydrogenated to form 1,3-propanediol (for the synthesis of step growth polymers) or transformed into simple organic motifs. Although much effort is being placed on the fermentation route to malonic acid, the potential uses are limited: by transforming malonic acid into the malonamide ligand, and proving its use in synthetically desirable catalytic transformations, we can expose a new market for malonic acid. Thus, bio-derived malonic acid has a new use. This will benefit the producers of biomass (large scale agriculture) and companies specialising in fermentation of biomass by facilitating a new customer base for their product (i.e. pharmaceutical industry).
 
Description A novel method to make phosphorus-phosphorus bonds using iron catalysts- this has never been reported using iron before. Discovering that we could undertake this transformation we have been able to extend it to other dehydrogenation reactions and on top of this we have been able to understand how the reactions take place, which allowed further reaction development.
Catalyst-free methods of making carbon-phosphorus bonds under mild conditions, which lead to an invited publication in a special edition of a journal. These carbon-phosphrus compounds may be of interest to the fine chemicals industry or for further chemical bond transformations making them into more elaboration phosphorus compounds.
We have shown that it is possible to generate high quality in situ NMR data and therefore undertake kinetic studies to understand the mechanism of iron catalysed reactions. Prior to our work in this area it was widely assumed that iron chemistry was not particularly amenable to NMR analysis due to paramagentism.
Similarly, we have shown that the carbon-phosphorus compounds we have synthesised can be easily isolated in air on the bench, again the literature widely reported that this was not possible and protection of the phosphorus as the borane adduct was necessary.
Exploitation Route We are investigating the potential of developing AI approaches to select the appropriate phosphorus-containing compounds, including those developed in our lab, and have applied for funding for this. In order to bolster this funding application I have received in-kind funding from an SME who are, in general, interested in our iron catalysis and phosphorus chemistry.
Our hydrogen-release chemistry has the potential in energy/fuel and advanced materials applications, but we need to develop this chemistry further before it could be taken up by others- this is a long term goal.
Sectors Chemicals,Energy

 
Description Royal Society Research Grant
Amount £13,985 (GBP)
Funding ID RG150510 
Organisation The Royal Society 
Sector Charity/Non Profit
Country United Kingdom
Start 03/2016 
End 03/2017
 
Title DFT study of ß-diketiminato iron(II) alkyl and phosphido complexes 
Description Article title: Facile, catalytic dehydrocoupling of phosphines using ß-diketiminato iron(II) complexes Journal: Chemistry, a European Journal DOI: 10.1002/chem.201503399 Authors: Andrew K. King, Antoine Buchard, Mary F. Mahon and Ruth L. Webster* DFT study: - Optimised geometries and computed free enthalpies of ß-diketiminato iron(II) alkyl and phosphido complexes depending on their spin state. - Thermodynamics of reaction between ß-diketiminato iron(II) alkyl complex and diphenylphosphine. - Thermodynamics of dimerization reaction of (DIPPNacnac)FePPh2 Protocol: uPBE1PBE/6-311+G(d) (Fe+core ligand)-6-31g(d) (rest of the molecule)/cpcm=benzene/T=343.15K (see basis_set.jpg) except : - [(DIPPNacnac)FePPh2]2 : 6-31g(d) for all atoms - (DIPPNacnac)FePPh2_M062X_m=5 used uM062XE/SDD (Fe)-6-311+G(d) (core ligand)-6-31g(d) (rest of the molecule)/cpcm=benzene/T=343.15K Content: Gaussian09 rev D.01 output files; basis_set.jpg (illustration of basis sets used) 
Type Of Material Database/Collection of data 
Year Produced 2015 
Provided To Others? Yes  
URL https://figshare.com/articles/dataset/DFT_study_of_diketiminato_iron_II_alkyl_and_phosphido_complexe...
 
Description Iron Catalysis for the Synthesis of Ligands: a Ligand Knowledge Database with Industrial Applications 
Organisation CatScI
Country United Kingdom 
Sector Private 
PI Contribution PDRA (Maialen Espinal-Viguri) to investigate industrial application of phosphines prepared by iron catalysis developed through EPSRC First Grant (Impact Acceleration Award).
Collaborator Contribution Industrial expertise- target driven catalytic applications
Impact Project will commence in April 2016
Start Year 2015