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二有机碲氧鎓(IV)阳离子{[2,6-(CHNMe)CHTe(μ-O)]}与三氯(二甲基亚砜)铂(II)阴离子的结构

Structure of a diorganotelluroxonium(IV) cation, {[2,6-(CHNMe)CHTe(μ-O)]}, with the tri-chlorido-(dimethyl sulfoxide)-platinum(II) anion.

作者信息

Gupta Anand, Deka Rajesh, Butcher Ray J, Singh Harkesh B

机构信息

Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400 076, India.

Department of Chemistry, Howard University, 525 College Street NW, Washington DC 20059, USA.

出版信息

Acta Crystallogr E Crystallogr Commun. 2020 Aug 28;76(Pt 9):1520-1524. doi: 10.1107/S2056989020011482. eCollection 2020 Sep 1.

Abstract

In the title salt, di-μ-oxido-bis-{2,6-bis-[(di-methyl-amino)-meth-yl]phenyl-κ }tellurium(-IV) bis[tri-chlorido-(dimethyl sulfoxide-κ)platinate(II)], (CHNOTe)[PdCl(CHOS)], which crystallizes in the triclinic space group , each Te atom is in a distorted five-coordinated TeONC square-pyramidal geometry (τ values of 0.026 and 0.001) with the C atoms of the phenyl rings occupying the apical positions. The phenyl rings in the [CHNOTe] cation are in a arrangement to enable this species to participate in Te⋯Cl cation-anion inter-actions. There are also C-H⋯O inter-actions involving the dimethyl sulfoxide ligands and numerous cation-anion and anion-anion C-H⋯Cl inter-actions, which link the ions into a complex three-dimensional array.

摘要

在标题盐二-μ-氧代-双-{2,6-双-[(二甲基氨基)甲基]苯基-κ}碲(IV)双[三氯-(二甲基亚砜-κ)铂酸盐(II)],即(CHNOTe)[PdCl(CHOS)]中,其结晶于三斜空间群 ,每个碲原子处于扭曲的五配位TeONC四方锥几何构型(τ值分别为0.026和0.001),苯环的碳原子占据顶端位置。[CHNOTe]阳离子中的苯环呈 排列,以使该物种能够参与碲⋯氯阳离子 - 阴离子相互作用。还存在涉及二甲基亚砜配体的C - H⋯O相互作用以及众多阳离子 - 阴离子和阴离子 - 阴离子C - H⋯Cl相互作用,这些相互作用将离子连接成复杂的三维阵列。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dde9/7472760/f65fa4c0750c/e-76-01520-fig1.jpg

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