Isomerism and nuclearity control in bis(lawsonato)zinc(II) complexes

This work aims to provide new insights concerning isomerism and nuclearity control in lawsone complexation reactions, as well as exploit physical and chemical properties related to different structural features. Three new bis(lawsonato)zinc(II) complexes, cis,cis,cis-[ZnL2(H2O)(2)]center dot 2H(2)O (1), trans,trans,trans-[ZnL2(H2O)(2)] (2) and [Zn2L4(py)(2)]center dot 2H(2)O (3), were synthesized and characterized by X-ray crystallography, thermogravimetric analysis, H-1 NMR, IR and UV-Vis spectroscopies and cyclic voltammetry. It has been demonstrated that, for the reaction between zinc(II) and lawsone, the coordination geometry and nuclearity of the product can be directed by modifying the addition sequence of the reactants and the nature of the base (pyridine versus triethylamine). Complex 1 has a zinc(II) ion coordinated by two lawsonate anions and two water molecules in a cis configuration, in a distorted octahedral environment. On the other hand, the structure of 2 differs from 1 mainly by the trans conformation of the ligands. Complex 3 has a dinuclear structure with an inversion center lying between the two metal centers, where each one of the two zinc atoms is coordinated by two lawsonate anions in a cis configuration and by one pyridine molecule. When dissolved in dmso, however, all data indicate that complexes 1-3 are converted to one single species, [ZnL2(dmso)(2)]. (c) 2012 Elsevier Ltd. All rights reserved.