EPSRC Reference: |
GR/M09988/01 |
Title: |
ALKYL MIGRATION ROUTES FOR THE CATALYTIC AMINATION OF ALKENES |
Principal Investigator: |
Brown, Dr JM |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
Oxford Chemistry |
Organisation: |
University of Oxford |
Scheme: |
Standard Research (Pre-FEC) |
Starts: |
01 November 1998 |
Ends: |
31 January 2002 |
Value (£): |
153,498
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EPSRC Research Topic Classifications: |
Catalysis & Applied Catalysis |
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EPSRC Industrial Sector Classifications: |
Pharmaceuticals and Biotechnology |
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Related Grants: |
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Panel History: |
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Summary on Grant Application Form |
The key C-C bond-forming step in alkene hydroformylation involves the migration of an alkyl group from the metal to co-ordinated CO, thus forming a metal-acyl. Although some minor analogous changes have been carried out (e.g. in silylformylation) no work has been carried out in which the alkyl acceptor is varied from CO. We present a case that readily accessible metal nitrides have the potential to act as CO equivalents in catalytic reactions, and that the overall result would be a controlled introduction of a functional nitrogen atom into the alkene of other organic reactant. The experimental approach would build on our experience in homogeneous catalysts, identifying candidate nitrides nitrides and gaining information on their reactivity towards potential catalysts with emphasis on rhodium, but also in Ru, Pd and Pt chemistry. That phase would be followed by efforts to translate the observations into viable catalytic chemistry, using simple alkenes (vinylarenes, cycloalkenes) and hydrogen as the reductant. In this the nitrene would function stoichiometrically, but further efforts would be directed to determining whether a reaction catalytic in nitride could be achieved so that an accessible nitrogen source could be coupled to a regenerable nitride.
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Key Findings |
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Potential use in non-academic contexts |
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Impacts |
Description |
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Summary |
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Date Materialised |
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Sectors submitted by the Researcher |
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Project URL: |
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Further Information: |
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Organisation Website: |
http://www.ox.ac.uk |