Issue 42, 2013

Formation of a dicationic ruthenium benzyl complex by halide abstraction from a Grubbs-type second-generation benzylidene

Abstract

A ruthenium benzylidene complex with a neutral bidentate N-heterocyclic carbene was prepared and evaluated in ring-closing metathesis of diallyl substrates. Reaction with AgPF6 to generate a four-coordinate complex produced an unexpected dicationic ruthenium benzyl degradation product through nucleophilic attack of the NHC ligand on the benzylidene carbon.

Graphical abstract: Formation of a dicationic ruthenium benzyl complex by halide abstraction from a Grubbs-type second-generation benzylidene

Supplementary files

Article information

Article type
Communication
Submitted
14 Jun 2013
Accepted
28 Aug 2013
First published
30 Aug 2013

Dalton Trans., 2013,42, 14955-14958

Formation of a dicationic ruthenium benzyl complex by halide abstraction from a Grubbs-type second-generation benzylidene

T. G. Larocque, A. C. Badaj and G. G. Lavoie, Dalton Trans., 2013, 42, 14955 DOI: 10.1039/C3DT52357H

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