Thermodynamics of Solvation of Silver(I) Ion in Nonaqueous Solvents

IF 0.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
I. A. Kuz’mina, M. A. Kovanova
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引用次数: 0

Abstract

The Gibbs energies of the transfer of the silver(I) ion from methanol (MeOH) to dimethyl sulfoxide (DMSO) and from ethanol (EtOH) to N,N-dimethylformamide (DMF) were determined by potentio-metry. Our own and literature data on the thermodynamic characteristics of the transfer of Ag+ from alcohols (S1) to aprotic (S2) solvents were summarized and analyzed. It has been established that the replacement of amphoteric solvents with aprotic ones leads to significantly increased solvation of the silver(I) ion. The enthalpy contribution to the Gibbs energy of ion transfer in the case of the replacement (S1 → S2) is dominant. The strengthening of solvate complexes of Ag+ with solvent in the case of the replacement of S1 by S2 is caused mainly by an increase in the electron donor-acceptor (EDA) interactions due to a decrease in the acidity of solvents.

银(I)离子在非水溶剂中的溶解热力学
通过电位测定法测定了银离子从甲醇(MeOH)转移到二甲基亚砜(DMSO)和从乙醇(EtOH)转移到 N,N-二甲基甲酰胺(DMF)的吉布斯能。总结并分析了我们自己和文献中关于 Ag+ 从醇类(S1)转移到非沸腾(S2)溶剂的热力学特性的数据。结果表明,将两性溶剂替换为非沸腾溶剂会显著提高银离子的溶解度。在置换(S1 → S2)的情况下,离子转移的吉布斯能的焓贡献占主导地位。在 S1 被 S2 取代的情况下,Ag+ 与溶剂的溶解络合物的增强主要是由于溶剂酸性的降低导致电子供体-受体(EDA)相互作用的增加。
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来源期刊
CiteScore
1.20
自引率
14.30%
发文量
376
审稿时长
5.1 months
期刊介绍: Russian Journal of Physical Chemistry A. Focus on Chemistry (Zhurnal Fizicheskoi Khimii), founded in 1930, offers a comprehensive review of theoretical and experimental research from the Russian Academy of Sciences, leading research and academic centers from Russia and from all over the world. Articles are devoted to chemical thermodynamics and thermochemistry, biophysical chemistry, photochemistry and magnetochemistry, materials structure, quantum chemistry, physical chemistry of nanomaterials and solutions, surface phenomena and adsorption, and methods and techniques of physicochemical studies.
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