Water reorientation in the hydration shells of hydrophilic and hydrophobic solutes

被引:12
|
作者
Laage, Damien [1 ]
Stirnemann, Guillaume [1 ]
Hynes, James T. [1 ,2 ]
机构
[1] Ecole Normale Super, Dept Chem, Paris, France
[2] Univ Colorado, Dept Chem & Biochem, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
hydrogen-bond; water; reorientation; jump model; HYDROGEN-BOND DYNAMICS; HCL ACID IONIZATION; MOLECULAR-MECHANISM; LIQUID WATER; ENERGY; SPECTROSCOPY; SIMULATION; CONSTANTS;
D O I
10.1007/s11433-010-3215-y
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
We discuss some key aspects of our recent theoretical work on water reorientation dynamics, which is important in a wide range of phenomena, including aqueous phase chemical reactions, protein folding, and drug binding to proteins and DNA. It is shown that, contrary to the standard conception that these dynamics are diffusional, the reorientation of a water molecule occurs by sudden, large amplitude angular jumps. The mechanism involves the exchange of one hydrogen bond for another by the reorienting water, and the process can be fruitfully viewed as a chemical reaction. The results for reorientation times, which can be well described analytically, are discussed in the context of the molecular level interpretation of recent ultrafast infrared spectroscopic results, focusing on the concepts of structure making/breaking and solvent 'icebergs'.
引用
收藏
页码:1068 / 1072
页数:5
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