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首页> 外文期刊>Journal of physical chemistry letters >Quantitative Temperature Dependence of the Microscopic Hydration Structures Investigated by Ultraviolet Photodissociation Spectroscopy of Hydrated Phenol Cations
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Quantitative Temperature Dependence of the Microscopic Hydration Structures Investigated by Ultraviolet Photodissociation Spectroscopy of Hydrated Phenol Cations

机译:通过水合酚阳离子紫外线光化光谱研究的微观水化结构的定量温度依赖性

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To discuss the temperature effect on microscopic hydration structures in clusters, relative populations of the isomers having different hydration structures at welldefined temperatures are quite important. In the present study, we measured ultraviolet photodissociation spectra of the temperature-controlled hydrated phenol cation [PhOH(H2O)(5)](+) trapped in the 22-pole ion trap. Two isomers having a distinct hydration motif with each other are identified in the spectra, and a clear change in the relative populations is observed in the temperature range from 30 to 150 K. This behavior is quantitatively interpreted by statistical mechanical estimation based on density functional theory calculations. A ring with tail-type hydration motif is dominant in cold conditions, whereas a chain-like motif is dominant in hot conditions. The present study provides very quantitative information about the temperature effect on the microscopic hydration structures.
机译:为了讨论簇中对微观水化结构的温度效应,在井义温度下具有不同水合结构的异构体的相对群体非常重要。 在本研究中,我们测量了在22极离子阱中捕获的温度控制的水合酚阳离子[PHOH(H2O)(5)](+)的紫外线光积极。 在光谱中鉴定出具有不同水合基序的两种异构体,在30至150k的温度范围内观察到相对群体的透明变化。通过基于密度函数理论,通过统计机械估计定量解释该行为 计算。 具有尾式水合基序的戒指在冷条件下显着,而链状基序在热条件下显着。 本研究提供了关于微观水化结构对温度效应的非常定量的信息。

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