Issue 10, 2013

Metal center dependent coordination modes of a tricarbene ligand

Abstract

The reaction of the benzene derived trisimidazolium salt [1](PF6)3 with [PdCl(allyl)]2 gave complex [2](PF6)3 featuring three Pd(allyl) moieties sandwiched between two tricarbene ligands, whereas the reaction of [1](PF6)3 with [M(Cp*)(Cl)2]2 (M = Ir, Rh) resulted in the formation of dinuclear MIII complexes [3]PF6 (M = Ir) and [4]PF6 (M = Rh) where each metal center is coordinated by an NHC donor and orthometallates the central phenyl ring. The remaining imidazolium group in [4]PF6 can be metallated with [Rh(Cp*)(Cl)2]2 to give the trinuclear triply orthometallated complex [5].

Graphical abstract: Metal center dependent coordination modes of a tricarbene ligand

Supplementary files

Article information

Article type
Communication
Submitted
12 Oct 2012
Accepted
11 Dec 2012
First published
12 Dec 2012

Chem. Commun., 2013,49, 1011-1013

Metal center dependent coordination modes of a tricarbene ligand

R. Maity, A. Rit, C. Schulte to Brinke, C. G. Daniliuc and F. E. Hahn, Chem. Commun., 2013, 49, 1011 DOI: 10.1039/C2CC37446C

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