Two isomorphous transition metal complexes displaying a coordinated tetrathionate unit: Bis(4,4′-dimethyl-2,2′-bipyridine- κ2 N,N′)(tetrathionato-κ2 S,S′)cadmium(II) dimethylformamide disolvate and the zinc(II) analogue
The isomorphous title compounds, [Tr(S4O6)(C 12H12N2)2]·2C 3H7NO (Tr = CdII and ZnII), consist of metal centres to which one tetrathionate and two 4,4′-dimethyl-2, 2′-bipyridine chelating ligands bind. The structures are completed by two symmetry-related dimethylformamide solvent molecules. Each met...
| Autores: | , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2013 |
| País: | Argentina |
| Institución: | Universidad Nacional de Buenos Aires. Facultad de Ciencias Exactas y Naturales |
| Repositorio: | Biblioteca Digital (UBA-FCEN) |
| Idioma: | inglés |
| OAI Identifier: | paperaa:paper_01082701_v69_n7_p745_Harvey |
| Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_01082701_v69_n7_p745_Harvey |
| Access Level: | acceso abierto |
| Palabra clave: | Bipyridine ligands Chelating ligands Covalent radii Point of views Solvent molecules Tetrathionate Title compounds Torsion angle Cadmium Chelation Dimethylformamide Metal complexes Metals Zinc compounds Ligands |
| Sumario: | The isomorphous title compounds, [Tr(S4O6)(C 12H12N2)2]·2C 3H7NO (Tr = CdII and ZnII), consist of metal centres to which one tetrathionate and two 4,4′-dimethyl-2, 2′-bipyridine chelating ligands bind. The structures are completed by two symmetry-related dimethylformamide solvent molecules. Each metal-centred complex is bisected by a twofold axis running through the metal centre and halving the chelating tetrathionate dianion through the central S - S bond. The ancillary symmetry-related 4,4′-dimethyl-2,2′-bipyridine ligands act as chelates. This results in a distorted six-coordinate geometry, with similar Tr - O/N distances but central angles differing substantially from 90 and 180°. Both ligands are basically featureless from a geometric point of view, with torsion angles in both coordinated tetrathionate groups suggesting a trend linking metal size (covalent radius) and ligand 'openness'. Packing is directed by (C - H)aromatic⋯O bridges and π-π offset stacked interactions defining chains along [001], further linked by weaker (C - H)methyl⋯O bridges, some of them mediated by the dimethylformamide solvent molecules. © 2013 International Union of Crystallography. |
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