假聚铊(I)二异戊基二硫代磷酸盐[Tl{S2P(O-iso-С5H11)2}]:合成、结构组织(次生 Tl⋅⋅S 和 Tl⋅⋅O 相互作用在超分子自组装中的作用)和热行为

IF 1.1 3区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR
O. A. Bredyuk, I. A. Lutsenko, Yu. V. Nelyubina, S. V. Zinchenko, A. V. Ivanov
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引用次数: 0

摘要

摘要 通过单晶 XRD(CIF 文件 CCDC 编号:2296421)、同步热分析 (STA)、多核 (1H、13C、31P) NMR 和红外光谱,合成了晶体状假聚合铊(I)二异戊基二硫代磷酸酯 (Dtph),即 [Tl{S2P(O-iso-С5H11)2}] (I)。在这两种分子中,Dtph 配体的 S,S ′-异配位(Tl-S 键长度为 3.006-3.092 Å),从而形成了具有显著平均 P-S 键长度(1.966-1.985 Å)的小尺寸四元金属环 [TlS2P](一种 "蝴蝶 "构象)。分子 A 和分子 B 在结构上是有序的,它们由两种类型的超分子链(⋅⋅A⋅⋅⋅A⋅⋅⋅A⋅⋅⋅⋅)n 和(⋅⋅B⋅⋅⋅⋅B⋅⋅⋅⋅)n 构建而成,这些超分子链上的结构单元是由成对的次级 Tl⋅⋅⋅S 和 Tl⋅⋅⋅O 相互作用在链长上交替结合而成的。反过来,属于两条相邻假聚合链的分子 A 和分子 B 之间也会发生成对的次级(但较弱)Tl⋅⋅S 相互作用。这些相互作用的多重性促成了双超分子带的形成。在氩气环境下,利用 STA 技术对化合物 I 的热行为进行了研究。电子探针显微分析(EPMA)和扫描电子显微镜(SEM)被用来研究残留物质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pseudopolymeric Thallium(I) Di-iso-pentyl Dithiophosphate, [Tl{S2P(O-iso-С5H11)2}]: Synthesis, Structural Organization (Role of Secondary Tl⋅⋅⋅S and Tl⋅⋅⋅O Interactions in Supramolecular Self-Assembly), and Thermal Behavior

Pseudopolymeric Thallium(I) Di-iso-pentyl Dithiophosphate, [Tl{S2P(O-iso-С5H11)2}]: Synthesis, Structural Organization (Role of Secondary Tl⋅⋅⋅S and Tl⋅⋅⋅O Interactions in Supramolecular Self-Assembly), and Thermal Behavior

Pseudopolymeric Thallium(I) Di-iso-pentyl Dithiophosphate, [Tl{S2P(O-iso-С5H11)2}]: Synthesis, Structural Organization (Role of Secondary Tl⋅⋅⋅S and Tl⋅⋅⋅O Interactions in Supramolecular Self-Assembly), and Thermal Behavior

Crystalline pseudopolymeric thallium(I) di-iso-pentyl dithiophosphate (Dtph), [Tl{S2P(O-iso5H11)2}] (I), is synthesized and characterized in detail by single-crystal XRD (CIF file CCDC no. 2296421), simultaneous thermal analysis (STA), multinuclear (1H, 13C, 31P) NMR, and IR spectroscopy. Nonequivalent molecules of two types containing Tl(1) and Tl(2) atoms (hereinafter molecules А and В , respectively) are involved (1 : 1) in the formation of the structure of compound I. In both molecules, the S,S  ′-anisobidentate coordination of the Dtph ligands (Tl–S bond lengths 3.006–3.092 Å) results in the formation of small-size four-membered metallocycles [TlS2P] (a ‘butterfly’ conformation) with significantly averaged P–S bond lengths (1.966–1.985 Å). Molecules A and B are structurally ordered upon the construction of supramolecular chains of two types (⋅⋅⋅A⋅⋅⋅A⋅⋅⋅A⋅⋅⋅)n and (⋅⋅⋅B⋅⋅⋅B⋅⋅⋅B⋅⋅⋅)n with oppositely directed structural units combined by paired secondary Tl⋅⋅⋅S and Tl⋅⋅⋅O interactions alternating over the chain length. In turn, paired secondary (but weaker) Tl⋅⋅⋅S interactions occur between molecules A and B belonging to two neighboring pseudopolymeric chains. The multiplicity of these interactions provides the formation of double supramolecular ribbons. The thermal behavior of compound I is studied by the STA technique under an argon atmosphere. Thallium(I) tetrathiophosphate Tl3PS4 is identified as the only end product of the thermolysis of compound I. Electron probe microanalysis (EPMA) and scanning electron microscopy (SEM) are used to study the residual substance.

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来源期刊
Russian Journal of Coordination Chemistry
Russian Journal of Coordination Chemistry 化学-无机化学与核化学
CiteScore
2.40
自引率
15.80%
发文量
85
审稿时长
7.2 months
期刊介绍: Russian Journal of Coordination Chemistry is a journal that publishes reviews, original papers, and short communications on all aspects of theoretical and experimental coordination chemistry. Modern coordination chemistry is an interdisciplinary science that makes a bridge between inorganic, organic, physical, analytical, and biological chemistry.
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