Abstract

Two complexes formed in the reaction of dicobalt octacarbonyl with carbon disulphide were identified through X-ray crystallography as Co6C(CO)12S2(1) and [(CO)9Co3CS]2(2); the cluster core of (1) is composed of a trigonal prism of six cobalt atoms capped symmetrically by two sulphur atoms, and containing a carbide atom in the centre, whereas (2) is a trans-disulphide of the enneacarbonyltricobaltcarbon cluster, showing distortion of the idealized threefold local symmetry of the Co3CS entities presumably owing to repulsive interactions between the sulphur and (equatorial) carbonyl-C atoms.

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