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Correlation of the empirical polarity parameters of solvate ionic liquids (SILs) with molecular structure

机译:溶剂水离子液体液体(SILs)与分子结构的相关性的相关性

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摘要

Empirical polarity parameters for 10 solvate ionic liquids (SILs) have been determined using Catalan's probes. The solvation environment surrounding the probe molecules in the SILs is dependent on the mutual interactions between the cation, anion and chelating ligand, leading to characteristic values of the polarity parameters. The acidity of the SILs is comparable to the acidity of polar protic solvents, which is attributed to the ability of the Li cation to interact with the probe in a manner similar to H-bond donor. The choice of anion influenced the measured acidity of SILs by determining the extent of cation-probe interactions possible. The basicity showed a strong correlation with the nature of the anion but was also influenced by the extent of cation-anion interaction and choice of ligand. Temperature dependence of polarity parameters in SILs is relatively small, but shows some interesting trends. (C) 2019 Elsevier B.V. All rights reserved.
机译:使用加那甲烷的探针确定10个溶剂化物离子液体(SIL)的经验极性参数。 围绕SIL中探针分子的溶剂化环境取决于阳离子,阴离子和螯合配体之间的相互作用,导致极性参数的特征值。 SIL的酸度与极性质子溶剂的酸度相当,其归因于Li阳离子以类似于H键供体的方式与探针相互作用的能力。 阴离子的选择通过确定可能的阳离子探针相互作用的程度来影响SIL的测量酸度。 碱度与阴离子的性质表现出强烈的相关性,但也受到阳离子阴离子相互作用和配体的选择的影响。 SILS中极性参数的温度依赖性相对较小,但显示了一些有趣的趋势。 (c)2019 Elsevier B.v.保留所有权利。

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