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Bioinorganic Chemistry and Applications
Volume 3, Issue 1-2, Pages 69-80

Chances and Limits of the Coordination Chemistry with Bis(benzene-l,2-dithiolato) Ligands

Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster Wilhelm-Klemm-Straße 8, Münster D-48149, Germany

Copyright © 2005 Hindawi Publishing Corporation. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


The incorporation of benzene-l,2-dithiolato building blocks into supramolecular coordination assemblies is the main objective of the investigations described here. Special interest is directed towards dinuclear complexes with bis(benzene-l,2-dithiolato) ligands, which might be able to form helical structures. Bis(benzene-l,2-dithiolato) ligands are accessible by ortho-functionalization and subsequent linkage of two benzene-l,2-dithiol units. The preparation of well defined complexes of titanium, cobalt and nickel with bis(benzene-l,2-dithiolato) ligands requires strictly thermodynamic equilibration conditions. In that case the size and shape of the ligand backbone determine if dinuclear double-stranded or mononuclear chelate complexes are obtained. The dinuclear double-stranded complexes with Ni(II) and Ni(III) are characterized by a coplanar non-helical arrangement of the square-planar bis(benzene-l,2-dithiolato)nickelate moieties. The complete structural characterization of the series [M(C6H4S2-1,2)3]n- (n = 0, 1, 2) for molybdenum and tungsten indicates an interesting coordination chemistry of dinuclear triple-stranded complexes.