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Varying the metal/metal ratio in related Cu–Ca complexes
Authors:Fatima Zohra Chiboub Fellah  Jean-Pierre Costes  Françoise Dahan  Carine Duhayon  Jean-Pierre Tuchagues
Institution:1. Laboratoire de Chimie de Coordination du CNRS, UPR 8241, liée par conventions à l’Université Paul Sabatier et à l’Institut National Polytechnique de Toulouse, 205 route de Narbonne, 31077 Toulouse Cedex, France;2. Université Abou baker Belkaid, Faculté des Sciences, Département de Chimie, BP 119, 13000 Tlemcen, Algeria
Abstract:We demonstrate with the help of structural determinations and spectroscopic data that the nuclearity of Cu–Ca complexes derived from compartmental Schiff base ligands does not depend on the ionic radius of calcium. The main factors governing these reactions are the different affinities of the calcium ions for the anionic species present in solution: the tetradentate O2O2 coordination site of the ligand and the nitrato ions. Because these affinities do vary upon going from calcium to lanthanide ions, it is not possible to use the template effect of the trinuclear Cu–Ca–Cu complexes in order to prepare the corresponding Cu–Ln–Cu complexes.
Keywords:Compartmental Schiff base ligands  3d-Alkaline-earth heterometallic complexes  Dinuclear Cu&ndash  Ca complexes  Trinuclear Cu&ndash  Ca&ndash  Cu complexes  Single-crystal X-ray structures  Magnetic properties
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