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苯-水纳米团簇中质子化的红外光谱:疏水界面上的水合氢离子、Zundel 离子和 Eigen 离子。

IR spectroscopy of protonation in benzene-water nanoclusters: hydronium, zundel, and eigen at a hydrophobic interface.

机构信息

Department of Chemistry, University of Georgia , Athens, Georgia 30602, United States.

出版信息

J Am Chem Soc. 2012 Aug 8;134(31):13046-55. doi: 10.1021/ja3038245. Epub 2012 Jul 27.

Abstract

The structure of ions in water at a hydrophobic interface influences important processes throughout chemistry and biology. However, experiments to measure these structures are limited by the distribution of configurations present and the inability to selectively probe the interfacial region. Here, protonated nanoclusters containing benzene and water are produced in the gas phase, size-selected, and investigated with infrared laser spectroscopy. Proton stretch, free OH, and hydrogen-bonding vibrations uniquely define protonation sites and hydrogen-bonding networks. The structures consist of protonated water clusters binding to the hydrophobic interface of neutral benzene via one or more π-hydrogen bonds. Comparison to the spectra of isolated hydronium, zundel, or eigen ions reveals the inductive effects and local ordering induced by the interface. The structures and interactions revealed here represent key features expected for aqueous hydrophobic interfaces.

摘要

在疏水界面处,水中离子的结构会影响化学和生物学中的许多重要过程。然而,用于测量这些结构的实验受到存在的构型分布以及无法选择性探测界面区域的限制。在此,通过气相法制备了含有苯和水的质子化纳米团簇,对其进行尺寸选择,并通过红外激光光谱进行了研究。质子伸缩、游离 OH 和氢键振动可唯一确定质子化位置和氢键网络。这些结构由质子化的水分子簇通过一个或多个π氢键与中性苯的疏水界面结合而成。与孤立的水合氢离子、溶剂化氢离子或自由氢离子的光谱进行比较,揭示了界面引起的诱导效应和局部有序性。这里揭示的结构和相互作用代表了预期的水-疏水环境的关键特征。

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