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Daulin Chen, Chian Sing Lai, Edward R. T. Tiekink
Crystal structures of 2,2′-bipyridine adducts of two cadmium O-alkyl dithiocarbonates: rationalisation of disparate coordination geometries based on different crystal packing environments
Two distinct coordination geometries are found in the structures of Cd(S2COR)2(2,2′-bipyridine). For R = CH2CH2OCH3 (1) a N2S2 donor set defines a distorted tetrahedral geometry for cadmium as the xanthate ligands adopt a monodentate coordination mode. By contrast, a N2S3 donor set is found in the structure where R is butyl (2) as one of the xanthate ligands is chelating. An analysis of the crystal structures shows that both lattices feature extensive C—H…π interactions and that in (1) there are C—H…O interactions that are not present in (2). In (2) there are π…π interactions that are absent in (1). A qualitative argument based on crystal packing considerations is proposed to explain the differences in molecular structures.
Zeitschrift für Kristallographie, Oldenbourg Wissenschaftsverlag
Print ISSN: 0044-2968
Volume: 218, 11/2003
Pages: 747