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A homolytic oxy-functionalization mechanism: intermolecular hydrocarbyl migration from M–R to vanadate oxo†
Mu-Jeng Cheng,Robert J. Nielsen,William A. Goddard III
Chemical Communications Pub Date : 07/28/2014 00:00:00 , DOI:10.1039/C4CC03067B
Abstract

A new mechanism for generating C–O bonds from metal-hydrocarbyls involving homolytic, intermolecular migration of the hydrocarbyl group to a vanadium oxo is reported. Responsible for the C–O bond in phenol formed by the reaction of OVCl3 with HgPh2, it may provide air-regenerable metal oxos a role in aerobic alkane oxidations.

Graphical abstract: A homolytic oxy-functionalization mechanism: intermolecular hydrocarbyl migration from M–R to vanadate oxo
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