Issue 14, 2008

Activation of two C–H bonds of NHC N-methyl groups on triosmium and triruthenium carbonyl clusters

Abstract

The thermolysis of the NHC triosmium cluster [Os3(Me2Im)(CO)11] (1a; Me2Im = 1,3-dimethylimidazol-2-ylidene) in toluene at reflux temperature sequentially affords the edge-bridged cluster [Os3(µ-H)(µ-κ2-MeImCH2)(CO)10] (2a) and the face-capped derivative [Os3(µ-H)232-MeImCH)(CO)9] (3a). These products result from the sequential oxidative addition of one (2a) and two (3a) N–methyl C–H bonds of the original NHC ligand. The related face-capped triruthenium cluster [Ru3(µ-H)232-MeImCH)(CO)9] (3b) has been prepared by heating the NHC triruthenium cluster [Ru3(Me2Im)(CO)11] (1b) in THF at reflux temperature. In this case, the pentanuclear derivatives [Ru5(Me2Im)(µ42-CO)(CO)14] (4b) and [Ru5(Me2Im)242-CO)(CO)13] (5b) are minor reaction products, but a ruthenium cluster analogous to 2a has not been obtained. The face-capped oxazole-derived NHC triruthenium cluster [Ru3(µ-H)232-OxCH)(CO)9] (3c; MeOx = N-methyloxazol-2-ylidene) is the only isolated product of the thermolysis of [Ru3(MeOx)(CO)11] (1c) in THF at reflux temperature

Graphical abstract: Activation of two C–H bonds of NHC N-methyl groups on triosmium and triruthenium carbonyl clusters

Supplementary files

Article information

Article type
Paper
Submitted
06 Dec 2007
Accepted
07 Feb 2008
First published
28 Feb 2008

Dalton Trans., 2008, 1937-1942

Activation of two C–H bonds of NHC N-methyl groups on triosmium and triruthenium carbonyl clusters

J. A. Cabeza, I. del Río, D. Miguel, E. Pérez-Carreño and M. G. Sánchez-Vega, Dalton Trans., 2008, 1937 DOI: 10.1039/B718770J

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