INVESTIGADORES
SUAREZ Sebastian
artículos
Título:
Two isomorphous transition metal complexes displaying a coordinated tetra­thio­nate unit: (bis­(4,4'-dimethyl-2,2'-bipyridine)-tetra­thio­nate- Tr, dimethyl­formamide solvate [Tr = Cadmium(II), Zinc(II) ].
Autor/es:
MIGUEL HARVEY; SEBASTIAN SUAREZ*; FABIO DOCTOROVICH; RICARDO BAGGIO
Revista:
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS
Editorial:
WILEY-BLACKWELL PUBLISHING, INC
Referencias:
Lugar: Londres; Año: 2013 vol. 69 p. 745 - 745
ISSN:
0108-2701
Resumen:
The isomorphous title compounds, [Tr(S4O6)(C12H12N2)2]- 2C3H7NO (Tr = CdII and ZnII), consist of metal centres to which one tetrathionate and two 4,40-dimethyl-2,20-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 4,40-dimethyl-2,20-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 ? 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.
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