溶剂化物络合物LiAlCl4·SO2:合成及其理化性质

IF 2.9 2区 化学 Q3 CHEMISTRY, PHYSICAL
Ludmila G. Golubyatnikova, Vadim Yu. Mishinkin, Dmitrii R. Garipov, Alfia R. Yusupova, Dmitrii.V. Kolosnitsyn, Elena V. Kuzmina* and Vladimir S. Kolosnitsyn, 
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引用次数: 0

摘要

本文介绍了LiAlCl4·SO2溶剂化物配合物的合成及其性质。用热重分析、拉曼光谱和紫外-可见光谱测定其成分。LiAlCl4·SO2的比离子电导率为4.7 × 10-2 S·cm-1。25℃时的动态粘度为19 cP,锂转移数为0.78。采用热重法和差示扫描量热法测定了LiAlCl4·SO2的熔点(+2.5℃)和分解温度(+60℃)。用分子动力学方法研究了溶剂化物配合物LiAlCl4·SO2的结构。锂离子由阴离子AlCl4 -中的一个Cl原子和SO2中的一个氧原子配位。LiAlCl4·SO2的锂离子配位数为4。锂离子由三个阴离子AlCl4 -和一个SO2分子配位。阴离子AlCl4 -作为桥接配体,结合不同的锂离子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Solvate Complex LiAlCl4·SO2: Synthesis and Physical-Chemical Properties

Solvate Complex LiAlCl4·SO2: Synthesis and Physical-Chemical Properties

This work describes the synthesis of the LiAlCl4·SO2 solvate complex and its properties. Its composition was determined using thermogravimetric analysis, Raman spectroscopy, and UV–vis spectroscopy. The specific ionic conductivity of LiAlCl4·SO2 is 4.7 × 10–2 S·cm–1. The dynamic viscosity is 19 cP at 25 °C, and the lithium transference number is 0.78. The melting point (+2.5 °C) and decomposition temperature (+60 °C) of LiAlCl4·SO2 were determined by simultaneous thermogravimetric analysis and differential scanning calorimetry. The structure of the solvate complex LiAlCl4·SO2 has been studied using a molecular dynamics method. A lithium cation is coordinated by one atom of Cl of the anion AlCl4 and one oxygen atom of SO2. The coordination number of lithium ions of LiAlCl4·SO2 is 4. The lithium cation is coordinated by three anions of AlCl4 and one molecule of SO2. Anion AlCl4 acts as a bridging ligand and binds different lithium cations.

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来源期刊
CiteScore
5.80
自引率
9.10%
发文量
965
审稿时长
1.6 months
期刊介绍: An essential criterion for acceptance of research articles in the journal is that they provide new physical insight. Please refer to the New Physical Insights virtual issue on what constitutes new physical insight. Manuscripts that are essentially reporting data or applications of data are, in general, not suitable for publication in JPC B.
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