Issue 21, 1996

Synthesis, structural characterisation, electron paramagnetic resonance and magnetic studies of homoleptic copper complexes of pyridonate ligands

Abstract

Three homoleptic copper(II) complexes have been prepared which feature 6-halogen-substituted 2-pyridonate ligands [{Cu2(xhp)4}n](n= 1, xhp = 6-chloro- or 6-bromo-2-pyridonate; n= 2, xhp = 6-fluoro-2-pyridonate). X-ray structural analysis of the complexes showed that for the chlorine- and bromine-substituted derivatives a dinuclear complex forms where the xhp ligands are arranged to give a dimeric unit with idealised D2d symmetry. For the fluorine-substituted ligand smaller steric requirements allow rearrangement to occur to give dinuclear units with approximate C4v symmetry, which can then dimerise giving tetrametallic molecules. The Cu ⋯ Cu contacts within these species are around 2.5 Å, and to investigate the nature of the Cu ⋯ Cu interaction variable-temperature EPR and magnetic studies were carried out. These revealed strong antiferromagnetic exchange between the S=½ centres; EPR also revealed a weak interdimer exchange which was not evident from susceptibility measurements.

Article information

Article type
Paper

J. Chem. Soc., Dalton Trans., 1996, 4077-4082

Synthesis, structural characterisation, electron paramagnetic resonance and magnetic studies of homoleptic copper complexes of pyridonate ligands

A. J. Blake, C. M. Grant, E. J. L. McInnes, F. E. Mabbs, P. E. Y. Milne, S. Parsons, J. M. Rawson and R. E. P. Winpenny, J. Chem. Soc., Dalton Trans., 1996, 4077 DOI: 10.1039/DT9960004077

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