Issue 1, 1984

The role of [2 + 2] cycloaddition-type reactions in catalysis. Activation of H—H, C—H and C[double bond, length as m-dash]C bonds by metal complexes

Abstract

It is argued that direct [2 + 2] cycloadditions and cycloreversions involving Mt[double bond, length as m-dash]C and C[double bond, length as m-dash]C species and quasi-metallacyclobutanes are the key steps in olefin metathesis. This theoretical concept is then extended in a novel fashion to describe the mechanisms of many other important reactions in homogeneous and heterogeneous catalysis, and especially the activation of C[double bond, length as m-dash]C, H—H and C—H bonds by metal–alkyl complexes where the metal ion is electron deficient and the alkyl ligand assumes ‘carbenoid’ character.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 1, 1984,80, 129-134

The role of [2 + 2] cycloaddition-type reactions in catalysis. Activation of H—H, C—H and C[double bond, length as m-dash]C bonds by metal complexes

J. G. Hamilton and J. J. Rooney, J. Chem. Soc., Faraday Trans. 1, 1984, 80, 129 DOI: 10.1039/F19848000129

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