Issue 6, 2014

Solvent promoted reversible cyclometalation in a tethered NHC iridium complex

Abstract

Reaction of [Ir(COD)(py–ItBu)]+ (py–ItBu = 3-tert-butyl-1-picolylimidazol-2-ylidene) with acetonitrile results in reversible intramolecular C–H bond activation of the NHC ligand and formation of [Ir(η21-C8H13)(py–ItBu′)(NCMe)]+. Coordinated COD acts as an internal hydride acceptor and acetonitrile coordination offsets the otherwise unfavourable thermodynamics of the process.

Graphical abstract: Solvent promoted reversible cyclometalation in a tethered NHC iridium complex

Supplementary files

Article information

Article type
Communication
Submitted
18 Oct 2013
Accepted
20 Nov 2013
First published
21 Nov 2013

Chem. Commun., 2014,50, 685-687

Solvent promoted reversible cyclometalation in a tethered NHC iridium complex

J. E. Wheatley, C. A. Ohlin and A. B. Chaplin, Chem. Commun., 2014, 50, 685 DOI: 10.1039/C3CC48015A

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