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FluoroFix SIGNED

Catalytic C–F Bond Functionalization for the Fixation of Environmentally Persistent Fluorocarbons

Total Cost €

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EC-Contrib. €

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Partnership

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Project "FluoroFix" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.ac.uk/

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website http://crimmingroup.org
 Total cost 1˙496˙925 €
 EC max contribution 1˙496˙925 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-STG
 Funding Scheme ERC-STG
 Starting year 2016
 Duration (year-month-day) from 2016-04-01   to  2021-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 1˙496˙925.00

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 Project objective

The objective of my project is to develop new methods to transform environmentally persistent hydrofluorocarbons (HFCs) and hydrofluoroolefins (HFOs), into reactive chemical building blocks that can be used in chemical manufacture. My team will achieve this by developing a series of new chemical reactions that transform inert carbon–fluorine bonds in HFCs or HFOs into reactive carbon–boron or carbon–aluminum bonds. My team will show that these reactive species can be used to construct carbon–carbon bonds. The idea is to develop a net series of reactions that results in the fixation of fluorine from low-value, volatile, and environmentally damaging organic molecules to high-value, non-volatile organic molecules. When successful, this approach should open up new routes that allow the chemical industry to repurpose HFCs and HFOs as chemical intermediates, and not end products, that complements European Union legislation. By the end of this project, my team will have pioneered methods for the production of agrochemicals and pharmaceuticals from environmentally persistent fluorocarbons.

 Publications

year authors and title journal last update
List of publications.
2019 Martí Garçon, Clare Bakewell, George A. Sackman, Andrew J. P. White, Richard I. Cooper, Alison J. Edwards, Mark R. Crimmin
A hexagonal planar transition-metal complex
published pages: 390-393, ISSN: 0028-0836, DOI: 10.1038/s41586-019-1616-2
Nature 574/7778 2020-02-04
2019 Greg Coates, Hui Yee Tan, Carolin Kalff, Andrew J. P. White, Mark R. Crimmin
Defluorosilylation of Industrially Relevant Fluoroolefins Using Nucleophilic Silicon Reagents
published pages: 12514-12518, ISSN: 1433-7851, DOI: 10.1002/anie.201906825
Angewandte Chemie International Edition 58/36 2020-02-04
2019 Nicholas A. Phillips, James O’Hanlon, Thomas N. Hooper, Andrew J. P. White, Mark R. Crimmin
Dihydridoboranes: Selective Reagents for Hydroboration and Hydrodefluorination
published pages: 7289-7293, ISSN: 1523-7060, DOI: 10.1021/acs.orglett.9b02515
Organic Letters 21/18 2020-02-04
2019 Thomas N. Hooper, Samantha Lau, Wenyi Chen, Ryan K. Brown, Martí Garçon, Karen Luong, Nathan S. Barrow, Andrew S. Tatton, George A. Sackman, Christopher Richardson, Andrew J. P. White, Richard I. Cooper, Alison J. Edwards, Ian J. Casely, Mark R. Crimmin
The partial dehydrogenation of aluminium dihydrides
published pages: 8083-8093, ISSN: 2041-6520, DOI: 10.1039/c9sc02750e
Chemical Science 10/35 2020-02-04
2019 Richard Y. Kong, Mark R. Crimmin
Reversible insertion of CO into an aluminium–carbon bond
published pages: 10.1039/c9cc0281, ISSN: 1359-7345, DOI: 10.1039/c9cc02818h
Chemical Communications 2019-06-06
2019 Nicholas Phillips, Andrew White, Mark Crimmin
Selective Hydrodefluorination of Hexafluoropropene to Industrially Relevant Hydrofluoroolefins
published pages: 10.1002/adsc.201, ISSN: 1615-4150, DOI: 10.1002/adsc.201900234
Advanced Synthesis & Catalysis 2019-06-06
2019 Clare Bakewell, Andrew J. P. White, Mark R. Crimmin
Reversible alkene binding and allylic C–H activation with an aluminium( i ) complex
published pages: 2452-2458, ISSN: 2041-6520, DOI: 10.1039/c8sc04865g
Chemical Science 10/8 2019-06-06
2019 Martí Garçon, Clare Bakewell, Andrew J. P. White, Mark R. Crimmin
Unravelling nucleophilic aromatic substitution pathways with bimetallic nucleophiles
published pages: 1805-1808, ISSN: 1359-7345, DOI: 10.1039/c8cc09701a
Chemical Communications 55/12 2019-06-06
2018 Martí Garçon, Andrew J. P. White, Mark R. Crimmin
Palladium-catalysed magnesiation of benzene
published pages: 12326-12328, ISSN: 1359-7345, DOI: 10.1039/C8CC06392C
Chemical Communications 54/87 2019-04-18
2018 Richard Y. Kong, Mark R. Crimmin
Carbon Chain Growth by Sequential Reactions of CO and CO 2 with [W(CO) 6 ] and an Aluminum(I) Reductant
published pages: 13614-13617, ISSN: 0002-7863, DOI: 10.1021/jacs.8b09761
Journal of the American Chemical Society 140/42 2019-04-18
2018 Thomas N. Hooper, Martí Garçon, Andrew J. P. White, Mark R. Crimmin
Room temperature catalytic carbon–hydrogen bond alumination of unactivated arenes: mechanism and selectivity
published pages: 5435-5440, ISSN: 2041-6520, DOI: 10.1039/c8sc02072h
Chemical Science 9/24 2019-04-18
2018 Clare Bakewell, Andrew J. P. White, Mark R. Crimmin
Reactions of Fluoroalkenes with an Aluminium(I) Complex
published pages: 6638-6642, ISSN: 1433-7851, DOI: 10.1002/anie.201802321
Angewandte Chemie International Edition 57/22 2019-04-18
2017 Samantha Lau, Bryan Ward, Xueer Zhou, Andrew J. P. White, Ian J. Casely, Stuart A. Macgregor, Mark R. Crimmin
Mild sp 2 Carbon–Oxygen Bond Activation by an Isolable Ruthenium(II) Bis(dinitrogen) Complex: Experiment and Theory
published pages: 3654-3663, ISSN: 0276-7333, DOI: 10.1021/acs.organomet.7b00632
Organometallics 36/18 2019-04-17

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