Gazitúa Marcela, Fuentealba Patricio, Contreras Renato, Ormazábal-Toledo Rodrigo
Centro de Química Médica, Facultad de Medicina, Clínica Alemana Universidad del Desarrollo , Código Postal 7710162, Santiago, Chile.
Departamento de Física, Facultad de Ciencias, Universidad de Chile , Casilla 653, Santiago, Chile.
J Phys Chem B. 2015 Oct 15;119(41):13160-6. doi: 10.1021/acs.jpcb.5b05305. Epub 2015 Oct 1.
We herein report on the effect that water molecules, present as impurities, in the vicinity of an ionic liquid model structure, may induce on the Lewis acidity/basicity patterns normally observed in these materials. Depending on the position and orientation of water, the Lewis acidity/basicity pattern changes from "normal distribution" (i.e., the basicity located at the anion moiety and the acidity located at the cation fragment) to "bifunctional distribution" (i.e., the acidity and basicity located at the cation moiety). In some specific cases, there appears a third Lewis acidity/basicity distribution, where water may bind both the cation and the anion of the ion pair; a response we tentatively call "amphoteric". These effects are clearly traced to the hydrogen bond formation ability of water to coordinate different regions of pure ionic liquids taken as references.
我们在此报告,作为杂质存在于离子液体模型结构附近的水分子,可能会对这些材料中通常观察到的路易斯酸度/碱度模式产生影响。根据水的位置和取向,路易斯酸度/碱度模式从“正态分布”(即碱度位于阴离子部分,酸度位于阳离子片段)转变为“双功能分布”(即酸度和碱度位于阳离子部分)。在某些特定情况下,会出现第三种路易斯酸度/碱度分布,其中水可能同时结合离子对的阳离子和阴离子;我们将这种响应暂称为“两性”。这些效应显然可归因于水与作为参考的纯离子液体的不同区域配位的氢键形成能力。