Full Paper
Di- or Trinuclear 3d–4f Schiff Base Complexes: The Role of Anions
Article first published online: 21 OCT 2008
DOI: 10.1002/ejic.200800750
Copyright © 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Costes, J.-P., Donnadieu, B., Gheorghe, R., Novitchi, G., Tuchagues, J.-P. and Vendier, L. (2008), Di- or Trinuclear 3d–4f Schiff Base Complexes: The Role of Anions. Eur. J. Inorg. Chem., 2008: 5235–5244. doi: 10.1002/ejic.200800750
Publication History
- Issue published online: 11 NOV 2008
- Article first published online: 21 OCT 2008
- Manuscript Received: 29 JUL 2008
Funded by
- NATO
Keywords:
- Anions;
- Schiff bases;
- Transition metals;
- Lanthanides;
- Heterometallic complexes
Abstract
We demonstrate through structural, spectroscopic, and magnetic studies that the main factors governing the nuclearity of M–Gd (M = Cu, Ni) complexes derived from compartmental Schiff base ligands are the different affinities of the lanthanide ions for the potential ligands and anions present in the reaction medium. In the eight examples studied, there is competition between the tetradentate O2O2 coordination site of the polydentate ligand and the anionic entities brought by the gadolinium salts. The strong affinity of nitrato anions for lanthanides yields dinuclear complexes and prevents formation of trinuclear entities, whereas the use of poorly coordinating anions such as triflates may yield either dinuclear or trinuclear complexes, depending on the 3d/4f ratio.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

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