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双(1,1 - 二甲基胍基)四水合二甲基锡(IV)双(硫酸盐)

Bis(1,1-dimethyl-guanidinium) tetra-aqua-dimethyl-tin(IV) bis-(sulfate).

作者信息

Boye Mouhamadou Sembene, Diasse-Sarr Aminata, Lebraud Eric, Guionneau Philippe

出版信息

Acta Crystallogr Sect E Struct Rep Online. 2012 Jan;68(Pt 1):m70. doi: 10.1107/S1600536811053761. Epub 2011 Dec 21.

DOI:10.1107/S1600536811053761
PMID:22259366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3254333/
Abstract

Single crystals of the title salt, (C(3)H(10)N(3))(2)Sn(CH(3))(2)(H(2)O)(4)(2), formed concomitantly with the already known Sn(CH(3))(3)SO(4)·2H(2)O. In the title structure, the Sn(IV) atom displays a slightly distorted octa-hedral coordination geometry defined by four O water atoms in the equatorial positions and two methyl groups in the axial positions. In the crystal, various O-H⋯O and N-H⋯O hydrogen-bonding inter-actions between the organic cation and the coordinated water mol-ecules as donors and the sulfate O atoms as acceptors result in a three-dimensional structure. The Sn(IV) atom is located on an inversion centre, resulting in half of the complex metal cation being in the asymmetric unit.

摘要

标题盐(C₃H₁₀N₃)₂Sn(CH₃)₂(H₂O)₄₂的单晶与已知的[Sn(CH₃)₃]₂SO₄·2H₂O同时形成。在标题结构中,Sn(IV)原子呈现出略微扭曲的八面体配位几何构型,由赤道位置的四个O水原子和轴向位置的两个甲基定义。在晶体中,有机阳离子与作为供体的配位水分子以及作为受体的硫酸根O原子之间存在各种O-H⋯O和N-H⋯O氢键相互作用,从而形成三维结构。Sn(IV)原子位于一个对称中心上,导致一半的复合金属阳离子处于不对称单元中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f7/3254333/52d527e645ae/e-68-00m70-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f7/3254333/5e20b067108f/e-68-00m70-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f7/3254333/52d527e645ae/e-68-00m70-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f7/3254333/5e20b067108f/e-68-00m70-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f7/3254333/52d527e645ae/e-68-00m70-fig2.jpg

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本文引用的文献

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A short history of SHELX.SHELX简史。
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