氢键
渗透(战争)
分子
化学物理
氢
碳氢化合物
疏水
疏水效应
化学
液态水
水的性质
材料科学
化学工程
有机化学
热力学
生物化学
物理
运筹学
工程类
作者
Lawrence F. Scatena,M. G. Brown,Geraldine L. Richmond
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2001-05-04
卷期号:292 (5518): 908-912
被引量:960
标识
DOI:10.1126/science.1059514
摘要
Vibrational studies that selectively probe molecular structure at CCl4/H2O and hydrocarbon/H2O interfaces show that the hydrogen bonding between adjacent water molecules at these interfaces is weak, in contrast to generally accepted models of water next to fluid hydrophobic surfaces that suggest strong hydrogen bonding. However, interactions between these water molecules and the organic phase result in substantial orientation of these weakly hydrogen-bonded water molecules in the interfacial region. The results have important implications for understanding water adjacent to hydrophobic surfaces and the penetration of water into hydrophobic phases.
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