Objective
Fluorinated organic molecules play a pivotal role in chemical manufacture. For example, it has been estimated that approximately 20-40% of pharmaceuticals and agrochemicals contain at least one fluorine atom. Despite the fact that perfluoroarenes - aromatic hydrocarbons in which every hydrogen atom is replaced with a fluorine atom - are an inexpensive abundant chemical feedstock they are rarely used in chemical manufacture. The strong carbon–fluorine bond provides an impasse to further chemical reactions. Here we propose to develop a new catalytic method to transform inert carbon–fluorine bonds in perfluoroarenes to reactive carbon–aluminium bonds. We will transform the aluminium-containing reactive intermediates into useful products through carbon–carbon and carbon–heteroatom bond forming reactions. The overall process represents an original underpinning technology to transform inert and chemically persistent fluorinated molecules into building blocks that can be used in chemical manufacture. The ultimate goal of this work is to create a fresh paradigm for using perfluoroarenes in pharmaceutical and agrochemical programmes. The proposed programme will provide world-class training in the areas of organometallic chemistry, homogeneous catalysis and mechanistic analysis. The long-term benefits will be felt in the areas of health and food sustainability.
Fields of science
- natural scienceschemical sciencesinorganic chemistryorganometallic chemistry
- natural scienceschemical sciencesinorganic chemistrytransition metals
- natural scienceschemical sciencesinorganic chemistrypost-transition metals
- natural scienceschemical sciencesinorganic chemistryhalogens
- natural scienceschemical sciencescatalysis
Programme(s)
Funding Scheme
MSCA-IF-EF-ST - Standard EFCoordinator
SW7 2AZ LONDON
United Kingdom