Issue 35, 2009

Synthesis of rhodium(I) and iridium(I) complexes of chiral N-heterocyclic carbenes and their application to asymmetric transfer hydrogenation

Abstract

Rhodium and iridium complexes of chiral NHC–phenolimine and NHC–amine ligands have been prepared and studied for asymmetric transfer hydrogenation. X-ray and NMR spectroscopy show that for NHC–phenolimine complexes abstraction of chloride results in a change in ligand coordination from NHC only to chelating NHC–imine. Complexes of NHC–amines are inactive for transfer hydrogenation, whereas complexes of NHC–phenolimines are active at room temperature for a range of aryl containing ketones. Enantioselectivity is very sensitive to the NHC N-substituent resulting in a switch in the predominant enantiomer.

Graphical abstract: Synthesis of rhodium(I) and iridium(I) complexes of chiral N-heterocyclic carbenes and their application to asymmetric transfer hydrogenation

Supplementary files

Article information

Article type
Paper
Submitted
11 May 2009
Accepted
24 Jun 2009
First published
22 Jul 2009

Dalton Trans., 2009, 7141-7151

Synthesis of rhodium(I) and iridium(I) complexes of chiral N-heterocyclic carbenes and their application to asymmetric transfer hydrogenation

G. Dyson, J. Frison, A. C. Whitwood and R. E. Douthwaite, Dalton Trans., 2009, 7141 DOI: 10.1039/B909290K

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