Abstract
The bidentate 1,3,4-thia-diazole ligand substituted by two 2-pyridyl rings (denoted L) has been found to produce the new monomeric title complex, [Co(C 12H 8N 4S) 2(H 2O) 2](BF 4) 2. The thia-diazole and pyridyl rings surrounding the Co atom are almost coplanar [dihedral angle = 4.35 (7)°]. The mean plane defined by these heterocyclic moieties makes a dihedral angle of 18.72 (6)° with the non-coordinated pyridyl ring. The Co 2+ cation, located at a crystallographic center of symmetry, is bonded to two ligands and two water mol-ecules in a trans configuration in an octa-hedral environment. The tetra-fluorido - borate ions can be regarded as free anions in the crystal lattice. Nevertheless, they are involved in an infinite two-dimensional network along the [010] and [101] directions of O - H⋯F hydrogen bonds. © Bentiss et al. 2011.
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CITATION STYLE
Bentiss, F., Capet, F., Lagrenée, M., Saadi, M., & El Ammari, L. (2011). Trans-Diaqua-bis-[2,5-bis-(pyridin-2-yl)-1,3,4-thia-diazole]cobalt(II) bis-(tetra-fluoridoborate). Acta Crystallographica Section E: Structure Reports Online, 67(7). https://doi.org/10.1107/S1600536811020125
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