Issue 9, 2007

Aerobic oxidation of alcohols and alkylaromatics with dioxygen catalysed by N-hydroxyphthalimide with vanadium co-catalysts

Abstract

[Bu4N]VO3 or a combination of vanadium complexes with chloride salts are attractive co-catalysts for oxidation reactions of organic compounds with dioxygen catalysed by N-hydroxyphthalimide. The role of the chloride additive relates to the formation of more labile six-coordinate vanadium complexes. The same effect is also observed with amines. Two catalytic systems based on NHPI/VO(acac)2 with LiCl or [Bu4N]Cl and NHPI/[Bu4N]VO3 are most effective in oxidation reactions of primary and secondary alcohols, but oxidation of alkylaromatics proceeds with conversion rates of from 14.4% in the case of toluene to 67.0% in the case of ethylbenzene and with different selectivities, dependent on the structure of the substrate.

Graphical abstract: Aerobic oxidation of alcohols and alkylaromatics with dioxygen catalysed by N-hydroxyphthalimide with vanadium co-catalysts

Article information

Article type
Paper
Submitted
15 Feb 2007
Accepted
14 May 2007
First published
11 Jun 2007

New J. Chem., 2007,31, 1668-1673

Aerobic oxidation of alcohols and alkylaromatics with dioxygen catalysed by N-hydroxyphthalimide with vanadium co-catalysts

P. J. Figiel and J. M. Sobczak, New J. Chem., 2007, 31, 1668 DOI: 10.1039/B702443F

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