Abstract
The SnIV atom in the centrosymmetric title complex, [Sn2(CH3)4(NCS)2(OH)2], adopts a distorted trigonal–bipyramidal coordination environment defined by two methyl C atoms and one bridging hydroxide group in the equatorial plane while the other bridging hydroxide group and the N atom of the thiocyanate anion are in the apical >positions. The dinuclear species are linked through O—H⋯S and C—H⋯ S hydrogen-bonding interactions into a three-dimensional network.
Highlights
[Sn2(CH3)4(NCS)2(OH)2], adopts a distorted trigonal–bipyramidal coordination environment defined by two methyl C atoms and one bridging hydroxide group in the equatorial plane while the other bridging hydroxide group and the N atom of the thiocyanate anion are in the apical >positions
The dinuclear species are linked through O—H S and C—H S
H atoms treated by a mixture of independent and constrained refinement max = 1.06 e Å3
Summary
Molloyb and Gabriele Kociok-Köhnb a Laboratoire de Chimie Minerale et Analytique (LACHIMIA), Departement de Chimie, Faculte des Sciences et Techniques, Universite Cheikh Anta Diop, Dakar, Senegal, and bDepartment of Chemistry, University of Bath, Bath BA2 7AY, England. R factor = 0.026; wR factor = 0.056; data-to-parameter ratio = 22.6. For structures containing the four-membered distannoxane [Sn(OH)]2 unit, see: Chandrasekhar et al (2007); Ng (1998). See: Cox & Wardell (1996); Okio et al. H atoms treated by a mixture of independent and constrained refinement max = 1.06 e Å3. Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: WM2689)
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