Crystal structures of 2,2′-bipyridine adducts of two cadmium O-alkyl dithiocarbonates: rationalisation of disparate coordination geometries based on different crystal packing environments

Verfasser / Beitragende:
[Daulin Chen, Chian Sing Lai, Edward R. T. Tiekink]
Ort, Verlag, Jahr:
2003
Enthalten in:
Zeitschrift für Kristallographie - Crystalline Materials, 218/11(2003-11-01), 747-752
Format:
Artikel (online)
ID: 378882295
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024 7 0 |a 10.1524/zkri.218.11.747.20300  |2 doi 
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245 0 0 |a Crystal structures of 2,2′-bipyridine adducts of two cadmium O-alkyl dithiocarbonates: rationalisation of disparate coordination geometries based on different crystal packing environments  |h [Elektronische Daten]  |c [Daulin Chen, Chian Sing Lai, Edward R. T. Tiekink] 
520 3 |a 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. 
540 |a © 2003 Oldenbourg Wissenschaftsverlag GmbH 
690 7 |a Crystallography  |2 nationallicence 
690 7 |a Inorganic chemistry  |2 nationallicence 
690 7 |a Organic chemistry  |2 nationallicence 
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700 1 |a Lai  |D Chian Sing  |4 aut 
700 1 |a Tiekink  |D Edward R. T.  |4 aut 
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