BOYE, Mouhamadou Sembene; DIASSE-SARR, Aminata; GROSJEAN, Arnaud; GUIONNEAU, Philippe

doi:10.1107/S1600536813000676

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BOYE, Mouhamadou Sembene

DIASSE-SARR, Aminata

GROSJEAN, Arnaud
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]

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Ce document a été publié dans

Acta Crystallographica Section E : Structure Reports Online [2001-2014]. 2013, vol. 69, n° 2, p. m110-m111

International Union of Crystallography

Résumé en anglais

he central SnIV atom of the pentanuclear title complex, {[Sn(CH3)3]3O2C(CH2)PO3[Sn(CH3)3(H2O)]2HO2C(CH2)PO3}, is located on a twofold rotation axis; due to symmetry, the H atom of the carboxyl group of the anion is disordered with a site occupancy of 0.5. The central SnIV atom is bonded to three methyl groups (one of which is disordered about the twofold rotation axis) and is symmetrically trans coordinated by two phosphonate groups with Sn-O = 2.2665 (12) Å while the other SnMe3 residues are asymmetrically trans coordinated with Sn-O = 2.1587 (12) and 2.3756 (13) Å for one residue and Sn-O = 2.1522 (12) and 2.4335 (12) Å for the other; the Sn-O distances involving two O atoms trans to carboxylate are longer than those trans to phosphonate groups. The Sn-C distances lie in a very narrow range [2.112 (2)-2.133 (3) Å]. The oxyanion behaves as a tetra-coordinating ligand. The bridging mode of the latter leads to the formation of layers parallel to (001) that are interconnected by O-H...O and C-H...O hydrogen bonds.< Réduire

Mots clés en anglais

Crystal structure

Poly[diaqua(µ4-carboxylatomethylphosphonato)(µ4-carboxymethylphosphonato)pentadecamethylpentatin(IV)]