Issue 4, 2012

Efficient oxidative coupling of 2,6-disubstituted phenol catalyzed by a dicopper(ii) complex

Abstract

Complexation of a rigid multi-pyridine ligand bis(2-pyridyl)-1,8-naphthyridine (bpnp) with [Cu2(TFA)4] (TFA = trifluoroacetate) resulted in the formation of a dinuclear copper(II) complex, namely [Cu2(bpnp)(μ-OH)(TFA)3] (1). This complex has been characterized by X-ray crystallographic, spectroscopic and elemental analyses. Complex 1 is an efficient catalyst for the oxidative coupling of various 2,6-disubstituted phenols with molecular oxygen. Yields and selectivity depend on the reaction conditions employed, the best results being obtained in isopropanol or dioxane at 90 °C with yields of >99%. Mechanistic pathway of the catalysis is discussed.

Graphical abstract: Efficient oxidative coupling of 2,6-disubstituted phenol catalyzed by a dicopper(ii) complex

Supplementary files

Article information

Article type
Paper
Submitted
07 Jun 2011
Accepted
06 Oct 2011
First published
24 Nov 2011

Dalton Trans., 2012,41, 1158-1164

Efficient oxidative coupling of 2,6-disubstituted phenol catalyzed by a dicopper(II) complex

B. Liao, Y. Liu, S. Peng and S. Liu, Dalton Trans., 2012, 41, 1158 DOI: 10.1039/C1DT11065A

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