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首页> 外文期刊>The Journal of Chemical Physics >II.Hydrogen bond switching dynamics:Multidimensional infrared spectroscopy of water.
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II.Hydrogen bond switching dynamics:Multidimensional infrared spectroscopy of water.

机译:II。氢键转换动力学:水的多维红外光谱。

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We use multidimensional infrared spectroscopy of the OH stretch of HOD in D_2O to measure the interconversion of different hydrogen bonding environments.The OH stretching frequency distinguishes hydrogen bonded (HB) and non-hydrogen-bonded (NHB) configurations by their absorption on the low (red) and high (blue) sides of the line shape.Measured asymmetries in the two dimensional infrared OH line shapes are manifestations of the fundamentally different spectral relaxations of HB and NHB.HB oscillators exhibit coherent oscillations within the hydrogen-bonded free energy well before undergoing activated baffler crossing,resulting in the exchange of hydrogen bonded partners.Conversely,NHB oscillators rapidly return to HB frequencies within 150 fs.These results support a picture where NHB configurations are only visited transiently during large fluctuations about a hydrogen bond or during the switching of hydrogen bonding partners.The results are not consistent with the presence of entropically stabilized dangling hydrogen bonds or a conceptual picture of water as a mixture of environments with varying hydrogen bond strength separated by barriers >kT.
机译:我们使用D_2O中HOD的OH延伸的多维红外光谱法来测量不同氢键环境的互变.OH延伸频率通过氢键(HB)和非氢键(NHB)的构型来区分,它们在低(二维红外OH线形中测得的不对称性是HB和NHB的光谱弛豫根本不同的表现.HB振荡器在氢键自由能内的相干振荡早于相反,NHB振荡器在150 fs内迅速返回到HB频率,这些结果支持一张图片,其中NHB构型仅在氢键的大波动或切换期间短暂地访问氢键伙伴的结果与熵的存在不一致稳定的悬空氢键或水的概念图,其中氢键强度的变化由势垒> kT分隔的环境混合而成。

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