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水中的氢键与OH伸缩光谱:六聚体(笼状)、液体表面、液体及冰

Hydrogen Bonding and OH-Stretch Spectroscopy in Water: Hexamer (Cage), Liquid Surface, Liquid, and Ice.

作者信息

Tainter C J, Ni Y, Shi L, Skinner J L

机构信息

Theoretical Chemistry Institute and Department of Chemistry, University of Wisconsin, Madison, Wisconsin 53706, United States.

出版信息

J Phys Chem Lett. 2013 Jan 3;4(1):12-7. doi: 10.1021/jz301780k. Epub 2012 Dec 13.

Abstract

We present a unified picture of how OH-stretch spectroscopy in water can be understood in terms of hydrogen bonding for the four systems listed in the title. To understand the strength, and hence OH-stretch frequency, of a hydrogen bond, it is crucial to consider the number of additional acceptor hydrogen bonds made by both the donor and acceptor molecules. This necessity for focusing on the hydrogen-bond environment of both donor and acceptor molecules follows from quantum chemical considerations and is related to the three-body interactions in water. Armed with this understanding we can make a detailed interpretation of the OH-stretch IR absorption spectrum of the cage conformer for HOD(D2O)5 and the imaginary part of the ssp OH-stretch sum-frequency spectrum of the surface of liquid D2O with dilute HOD.

摘要

我们给出了一个统一的图景,说明如何根据氢键来理解标题中列出的四个体系在水中的OH伸缩光谱。为了理解氢键的强度以及由此产生的OH伸缩频率,关键是要考虑供体和受体分子形成的额外受体氢键的数量。这种关注供体和受体分子氢键环境的必要性源于量子化学的考虑,并且与水中的三体相互作用有关。基于这种理解,我们可以对HOD(D2O)5笼状构象体的OH伸缩红外吸收光谱以及稀HOD存在下液态D2O表面的ssp OH伸缩和频光谱的虚部进行详细解释。

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