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

Chem Commun (Camb). 2014 Sep 28;50(75):10994-6. doi: 10.1039/c4cc03067b. Epub 2014 Aug 6.

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.