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观察溶解的非极性基团周围悬挂的水分子羟基键。

Observation of water dangling OH bonds around dissolved nonpolar groups.

作者信息

Perera P N, Fega K R, Lawrence C, Sundstrom E J, Tomlinson-Phillips J, Ben-Amotz Dor

机构信息

Department of Chemistry, Purdue University, West Lafayette, IN 47907, USA.

出版信息

Proc Natl Acad Sci U S A. 2009 Jul 28;106(30):12230-4. doi: 10.1073/pnas.0903675106. Epub 2009 Jul 20.

Abstract

We report the experimental observation of water dangling OH bonds in the hydration shells around dissolved nonpolar (hydrocarbon) groups. The results are obtained by combining vibrational (Raman) spectroscopy and multivariate curve resolution (MCR), to reveal a high-frequency OH stretch peak arising from the hydration shell around nonpolar (hydrocarbon) solute groups. The frequency and width of the observed peak is similar to that of dangling OH bonds previously detected at macroscopic air-water and oil-water interfaces. The area of the observed peak is used to quantify the number of water dangling bonds around hydrocarbon chains of different length. Molecular dynamics simulation of the vibrational spectra of water molecules in the hydration shell around neopentane and benzene reveals high-frequency OH features that closely resemble the experimentally observed dangling OH vibrational bands around neopentyl alcohol and benzyl alcohol. The red-shift of approximately 50 cm(-1) induced by aromatic solutes is similar to that previously observed upon formation of a pi-H bond (in low-temperature benzene-water clusters).

摘要

我们报告了溶解的非极性(烃)基团周围水合壳层中悬空的OH键的实验观察结果。这些结果是通过结合振动(拉曼)光谱和多元曲线分辨(MCR)获得的,以揭示非极性(烃)溶质基团周围水合壳层产生的高频OH伸缩峰。观察到的峰的频率和宽度与先前在宏观空气-水和油-水界面检测到的悬空OH键的频率和宽度相似。观察到的峰的面积用于量化不同长度烃链周围水悬空键的数量。新戊烷和苯周围水合壳层中水分子振动光谱的分子动力学模拟揭示了高频OH特征,其与实验观察到的新戊醇和苄醇周围的悬空OH振动带非常相似。芳香族溶质引起的约50 cm(-1)的红移与先前在形成π-H键时(在低温苯-水簇中)观察到的红移相似。

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