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硫酸氢根离子的离子液体的高粘度:拉曼光谱研究。

High viscosity of imidazolium ionic liquids with the hydrogen sulfate anion: a Raman spectroscopy study.

机构信息

Laboratório de Espectroscopia Molecular, Instituto de Química, Universidade de São Paulo CP 26077, CEP 05513-970, São Paulo, SP, Brazil.

出版信息

J Phys Chem B. 2012 Jun 21;116(24):7281-90. doi: 10.1021/jp302091d. Epub 2012 Jun 11.

DOI:10.1021/jp302091d
PMID:22646491
Abstract

Ionic liquids based on 1-alkyl-3-methylimidazolium cations and the hydrogen sulfate (or bisulfate) anion, HSO(4)(-), are much more viscous than ionic liquids with alkyl sulfates, RSO(4)(-). The structural origin of the high viscosity of HSO(4)(-) ionic liquids is unraveled from detailed comparison of the anion Raman bands in 1-ethyl-3-methylimidazolium hydrogen sulfate and 1-butyl-3-methylimidazolium hydrogen sulfate with available data for simple HSO(4)(-) salts in crystalline phase, molten phase, and aqueous solution. Two Raman bands at 1046 and 1010 cm(-1) have been assigned as symmetric stretching modes ν(s)(S═O) of HSO(4)(-), the latter being characteristic of chains of hydrogen-bonded anions. The intensity of this component increases in the supercooled liquid phase. For comparison purposes, Raman spectra of 1-ethyl-3-methylimidazolium ethyl sulfate and 1-butyl-3-methylimidazolium methyl sulfate have been also obtained. There is no indication of difference in the strength of hydrogen bond interactions of imidazolium cations with HSO(4)(-) or RSO(4)(-) anions. Raman spectra at high pressures, up to 2.6 GPa, are also discussed. Raman spectroscopy provides evidence that hydrogen-bonded anions resulting in anion-anion interaction is the reason for the high viscosity of imidazolium ionic liquids with HSO(4)(-). If the ionic liquid is exposed to moisture, these structures are disrupted upon absorption of water from the atmosphere.

摘要

基于 1-烷基-3-甲基咪唑阳离子和硫酸氢根(或双硫酸根)阴离子的离子液体比具有烷基硫酸盐的离子液体具有更高的粘性,RSO 4 (-)。通过详细比较 1-乙基-3-甲基咪唑硫酸氢盐和 1-丁基-3-甲基咪唑硫酸氢盐中的阴离子拉曼带与结晶相、熔融相和水溶液中简单 HSO 4 (-)盐的可用数据,揭示了 HSO 4 (-)离子液体高粘度的结构起源。两个在 1046 和 1010 cm(-1)处的拉曼带被分配为 HSO 4 (-)的对称伸缩模式 ν(s)(S═O),后者是氢键阴离子链的特征。该成分的强度在过冷液相中增加。为了比较目的,还获得了 1-乙基-3-甲基咪唑硫酸乙酯和 1-丁基-3-甲基咪唑硫酸甲酯的拉曼光谱。没有迹象表明与 HSO 4 (-)或 RSO 4 (-)阴离子相互作用的咪唑阳离子氢键相互作用的强度存在差异。还讨论了高达 2.6 GPa 的高压下的拉曼光谱。拉曼光谱提供的证据表明,导致阴离子-阴离子相互作用的氢键阴离子是具有 HSO 4 (-)的咪唑离子液体高粘度的原因。如果离子液体暴露在潮湿的环境中,这些结构会在吸收大气中的水分时被破坏。

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