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Role of attractive methane-water interactions in the potential of mean force between methane molecules in water

机译:有吸引力的甲烷-水相互作用在水中甲烷分子之间的平均力中的作用

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On the basis of a Gaussian quasichemical model of hydration, a model of non-van der Waals character, we explore the role of attractive methane-water interactions in the hydration of methane and in the potential of mean force between two methane molecules in water. We find that the hydration of methane is dominated by packing and a mean-field energetic contribution. Contributions beyond the mean-field term are unimportant in the hydration phenomena for a hydrophobic solute such as methane. Attractive solute-water interactions make a net repulsive contribution to these pair potentials of mean force. With no conditioning, the observed distributions of binding energies are super-Gaussian and can be effectively modeled by a Gumbel (extreme value) distribution. This further supports the view that the characteristic form of the unconditioned distribution in the high-epsilon tail is due to energetic interactions with a small number of molecules. Generalized extreme value distributions also effectively model the results with minimal conditioning, but in those cases the distributions are sufficiently narrow that the details of their shape are not significant. (c) 2008 American Institute of Physics.
机译:基于高斯水化的准化学模型(非范德华特征模型),我们探讨了有吸引力的甲烷-水相互作用在甲烷水化中的作用以及在水中两个甲烷分子之间的平均力的作用。我们发现甲烷的水合作用主要是堆积和平均场能量贡献。在甲烷等疏水性溶质的水合现象中,超出平均场项的贡献并不重要。有吸引力的溶质-水相互作用对这些平均力对势具有净排斥作用。在没有条件的情况下,观察到的结合能分布是超高斯分布,可以通过Gumbel(极值)分布有效地建模。这进一步支持了这样的观点,即高ε尾中的无条件分布的特征形式是由于与少量分子的能量相互作用。广义极值分布还可以使用最少的条件有效地对结果建模,但是在那些情况下,分布足够狭窄,以至于其形状的细节并不重要。 (c)2008年美国物理研究所。

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