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首页> 外文期刊>Angewandte Chemie >From Single Hydrogen Bonds to Extended Hydrogen-Bond Wires: Low-Dimensional Model Systems for Vibrational Spectroscopy of Associated Liquids
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From Single Hydrogen Bonds to Extended Hydrogen-Bond Wires: Low-Dimensional Model Systems for Vibrational Spectroscopy of Associated Liquids

机译:从单氢键到加氢键合金属丝:缔合液体振动光谱的低维模型系统

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摘要

It is fair to say that if we ever wish to understand the anomalous properties of water, we need to study hydrogen bonds. Such a statement is based on statistical mechanics, which tells us how to calculate the structure and the thermodynamic properties of fluids and dense liquids from the forces between the particles. However, in the case of complex associated liquids, such calculations present a formidable—if not even insurmountable—challenge, which largely reflects our still-limited understanding of the hydrogen-bonding phenomenon itself. More experimental research on hydrogen-bonded systems is required to develop a comprehensive, satisfactory theory for associated liquids. This Review gives an introduction to the latest experimental technique currently being used to study the ultrafast structural dynamics of hydrogen bonds, namely two-dimensional infrared spectroscopy, and its applications to hydrogen-bonded systems of systematically increasing complexity, starting from the single hydrogen bond of a diol to low-dimensional extended networks of stereoselectively synthesized polyalcohols.
机译:可以说,如果我们想了解水的异常性质,就需要研究氢键。这样的陈述是基于统计力学的,它告诉我们如何根据粒子之间的力来计算流体和稠密液体的结构和热力学性质。但是,对于复杂的伴生液体,这种计算提出了巨大的挑战,即使不是无法克服的挑战,这在很大程度上反映了我们对氢键现象本身仍然有限的理解。需要开发更多的氢键体系实验研究,以开发出一种令人满意的有关液体的综合理论。这篇综述介绍了目前用于研究氢键的超快结构动力学的最新实验技术,即二维红外光谱,及其从系统的单氢键开始,在系统地增加复杂性的氢键系统中的应用。二醇到立体选择性合成多元醇的低维扩展网络。

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