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Dibenzylazanium (oxalato-κ(2) O,O′)triphenylstannate(IV)
The title compound, (C(14)H(16)N)[Sn(C(6)H(5))(3)(C(2)O(2))], was synthesised by allowing C(2)O(4)(Bz(2)NH(2))(2) (Bz = benzyl) to react with SnPh(3)Cl. The asymmetric unit is built up by four SnPh(3)C(2)O(4) anions and four Bz(2)NH(2) cations which are related by a pseudo-inversion centre. Each Sn(...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379190/ https://www.ncbi.nlm.nih.gov/pubmed/22719388 http://dx.doi.org/10.1107/S1600536812021125 |
Sumario: | The title compound, (C(14)H(16)N)[Sn(C(6)H(5))(3)(C(2)O(2))], was synthesised by allowing C(2)O(4)(Bz(2)NH(2))(2) (Bz = benzyl) to react with SnPh(3)Cl. The asymmetric unit is built up by four SnPh(3)C(2)O(4) anions and four Bz(2)NH(2) cations which are related by a pseudo-inversion centre. Each Sn(IV) cation is five-coordinated by the three phenyl groups and two O atoms belonging to the chelating oxalate ligand; the coordination geometry is that of a distorted trigonal bipyramid. Anions and cations are linked through N—H⋯O hydrogen bonds into a layer structure parallel to (001). Moreover, the anion–cation pairs are associated by two bifurcated N—H⋯O hydrogen bonds, generating pseudo-dimers. One of the phenyl groups of one anion is disordered over two sets of sites in a 0.69:0.31 ratio. The Flack parameter value of 0.44 (1) indicates racemic twinning. |
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