期刊
JOURNAL OF MOLECULAR STRUCTURE
卷 875, 期 1-3, 页码 478-485出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.molstruc.2007.05.020
关键词
quadridentate ligand; diethylamine; symmetrical bonding; dithiocarbamate
A quadridentate ligand disodium bis(2,2'-dithiopiperazinato-2,2'-diamino diethylamine) Na2L2 and its self assembled transition metal complexes of the type, M-2(L-2)(2) ( M = Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), Cd(II) and Hg(II)} have been reported. The piperazine pivoted homodinuclear complexes have been characterized by a range of spectral, thermal, microanalytical and conductometric techniques. On the basis of IR and H-1 NMR data a symmetrical bidentate coordination of the dithiocarbamato moiety has been observed in all the cases. The TGA profile of the ligand exhibits two stage thermolytic pattern although the complexes decompose in three steps, respectively. Metal sulfide is found to be the end product. The formation of homodinuclear complexes has been ascertained on the basis of FAB mass spectral data and a probable fragmentation pattern has been proposed. On the basis of UV-visible spectroscopic results and room temperature magnetic moment data a tetrahedral geometry has been proposed for all the complexes except for the Ni(II) and Cu(II) which are found to be square-planar. (c) 2007 Elsevier B.V. All rights reserved.
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