Chances and limits of the coordination chemistry with bis(benzene-l,2-dithiolato) ligands.

Abstract:

: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(C(6)H(4)S(2) - 1,2)(3)](n) - (n = 0, 1, 2) for molybdenum and tungsten indicates an interesting coordination chemistry of dinuclear triple-stranded complexes.

journal_name

Bioinorg Chem Appl

authors

Seidel WW,Hahn FE

doi

10.1155/BCA.2005.69

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

69-80

eissn

1565-3633

issn

1687-479X

pub_type

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