Kobrak Mark N
Department of Chemistry, Brooklyn College and the Graduate Center of the City University of New York, 2900 Bedford Avenue, Brooklyn, New York 11210, USA.
J Phys Chem B. 2007 May 10;111(18):4755-62. doi: 10.1021/jp066112f. Epub 2007 Feb 14.
Ionic liquids represent a novel and poorly understood class of solvents, and one challenge in understanding these systems is how one should view the electrostatic character of solute-solvent interactions. The highly structured nature of a fused salt makes a dielectric continuum approximation difficult to implement, and there is no obvious connection between the structure of an individual ion and the polarization character of the medium. We address this problem by making the ansatz that rather than polarizing the medium, the solute may be viewed as intercalating in the charge distribution of the neat liquid such that the solvent screens the electric field of the solute. This approach allows derivation of an analytical expression for the distribution of solvent charge about the solute, and this distribution is found to be a close match to simulation data. The theory also predicts that the electrostatic character of solute-solvent interactions should be determined primarily by the number density of solvent ions, a prediction proven correct by analysis of existing experimental data. The approach represents a new model for the interpretation of solvation phenomena in ionic liquids.
离子液体是一类新型且了解甚少的溶剂,理解这些体系面临的一个挑战在于应如何看待溶质 - 溶剂相互作用的静电特性。熔融盐高度结构化的性质使得介电连续介质近似难以实施,而且单个离子的结构与介质的极化特性之间没有明显的联系。我们通过做出这样的假设来解决这个问题:溶质不是使介质极化,而是可以看作嵌入纯液体的电荷分布中,从而使溶剂屏蔽溶质的电场。这种方法能够推导出溶质周围溶剂电荷分布的解析表达式,并且发现这种分布与模拟数据非常吻合。该理论还预测溶质 - 溶剂相互作用的静电特性应主要由溶剂离子的数密度决定,对现有实验数据的分析证明了这一预测是正确的。这种方法代表了一种用于解释离子液体中溶剂化现象的新模型。