二硫代磷酸盐配合物[Pd{(RO)2PS2}2] (R = Et, Ph)的晶体结构和光学性质

IF 1.2 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
Y. A. Bryleva, A. V. Mikheylis, L. A. Glinskaya
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引用次数: 0

摘要

研究了新型[Pd{(PhO)2PS22}]配合物和已知的[Pd({EtO)2PS22}]配合物的分子和晶体结构。XRD数据表明,[Pd({RO)2PS22}] (R = Et, Ph)化合物在中心对称空间群中结晶,其晶体结构为单核络合分子。\({{(\text{EtO})}_{2}}\text{PS}_{2}^{-}\)和\({{(\text{PhO)}}_{2}}\text{PS}_{2}^{-}\)离子发挥S,S '给体双齿螯合作用,形成方形平面的PdS4配位核。研究了这些配合物溶液的电子吸收光谱;考虑了\({{(\text{RO})}_{2}}\text{PS}_{2}^{-}\)配体结构和溶剂极性对所研究化合物光学性质的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Crystal Structures and Optical Properties of the Dithiophosphate Complexes [Pd{(RO)2PS2}2] (R = Et, Ph)

Molecular and crystal structures of the novel [Pd{(PhO)2PS2}2] complex and the known [Pd{(EtO)2PS2}2] complex are studied. According to the XRD data, [Pd{(RO)2PS2}2] (R = Et, Ph) compounds crystallize in centrosymmetric space groups, and their crystal structures consist of mononuclear complex molecules. The \({{(\text{EtO})}_{2}}\text{PS}_{2}^{-}\) and \({{(\text{PhO)}}_{2}}\text{PS}_{2}^{-}\) ions perform an S,S′-donor bidentate-chelating function leading to the formation of square-planar PdS4 coordination cores. The electronic absorption spectra of the solutions of these complexes are studied; the influence of the \({{(\text{RO})}_{2}}\text{PS}_{2}^{-}\) ligand structure and the solvent polarity on the observed optical properties of the studied compounds is considered.

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来源期刊
Journal of Structural Chemistry
Journal of Structural Chemistry 化学-无机化学与核化学
CiteScore
1.60
自引率
12.50%
发文量
142
审稿时长
8.3 months
期刊介绍: Journal is an interdisciplinary publication covering all aspects of structural chemistry, including the theory of molecular structure and chemical bond; the use of physical methods to study the electronic and spatial structure of chemical species; structural features of liquids, solutions, surfaces, supramolecular systems, nano- and solid materials; and the crystal structure of solids.
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