A fluxional (CuN2O2)-N-I core: binding of a keto oxygen atom to Cu-I and Ag-I

Drew, M.G.B., Naskar, J.P., Chowdhury, S. and Datta, D. (2005) A fluxional (CuN2O2)-N-I core: binding of a keto oxygen atom to Cu-I and Ag-I. European Journal of Inorganic Chemistry (23). pp. 4834-4839. ISSN 1434-1948 doi: 10.1002/ejic.200500499

Abstract/Summary

[Cu(2-acetylpyridine)(2)]ClO4 (1), characterised here, has a novel Cu'N202 core in the solid state. Variable-temperature H-1 NMR studies show that the two chelate rings open up in solution at room temperature and the keto oxygen atoms dangle freely. As the temperature is lowered, the 0 atoms tend to bind to the metal atom. The corresponding silver(I) complex, [Ag(2-acetylpyridine)2]ClO4 (4), characterised by single-crystal X-ray crystallography, has an (AgN2)-N-I core in the solid state as well as in solution. Thus, while 1 is fluxional, 4 is not. In cyclic voltammetry, complex 1 displays a quasireversible Cu-II/I couple with a half-wave potential of 0.40 V vs. SCE. Complex I is easily oxidised by air and H2O2 in methanol to give rise to a dinuclear copper(II) complex where the ligand framework is not simple acetylpyridine. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005).