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Temperature effect on the small-to-large crossover lengthscale of hydrophobic hydration

机译:温度对疏水水合跨度变化的影响

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The thermodynamics of hydration is expected to change gradually from entropic for small solutes to enthalpic for large ones. The small-to-large crossover lengthscale of hydrophobic hydration depends on the thermodynamic conditions of the solvent such as temperature, pressure, presence of additives, etc. We attempt to shed some light on the temperature dependence of the crossover lengthscale by using a probabilistic approach to water hydrogen bonding that allows one to obtain an analytic expression for the number of bonds per water molecule as a function of both its distance to a solute and solute radius. Incorporating that approach into the density functional theory, one can examine the solute size effects on its hydration over the entire small-to-large lengthscale range at a series of different temperatures. Knowing the dependence of the hydration free energy on the temperature and solute size, one can also obtain its enthalpic and entropic contributions as functions of both temperature and solute size. These functions can provide some interesting insight into the temperature dependence of the crossover lengthscale of hydrophobic hydration. The model was applied to the hydration of spherical particles of various radii in water in the temperature range from T = 293.15 K to T = 333.15 K. The model predictions for the temperature dependence of the hydration free energy of small hydrophobes are consistent with the experimental and simulational data on the hydration of simple molecular solutes. Three alternative definitions for the small-to-large crossover length-scale of hydrophobic hydration are proposed, and their temperature dependence is obtained. Depending on the definition and temperature, the small-to-large crossover in the hydration mechanism is predicted to occur for hydrophobes of radii from one to several nanometers. Independent of its definition, the crossover length-scale is predicted to decrease with increasing temperature.
机译:预期水合的热力学将从小溶质的熵逐渐变为大溶质的焓。疏水水合的小到大交叉长度尺度取决于溶剂的热力学条件,例如温度,压力,添加剂的存在等。我们尝试通过概率方法揭示交叉长度尺度对温度的依赖性。与水氢键的结合使得人们可以获得每个水分子的键数作为其与溶质的距离和溶质半径的函数的解析表达式。将这种方法结合到密度泛函理论中,可以研究在一系列不同温度下,从小到大的整个长度范围,溶质尺寸对其水合作用的影响。知道水合自由能对温度和溶质尺寸的依赖性,人们还可以获得其焓和熵的贡献,这是温度和溶质尺寸的函数。这些功能可以为疏水水合的跨度长度尺度的温度依赖性提供一些有趣的见解。该模型应用于温度为T = 293.15 K至T = 333.15 K的水中各种半径的球形颗粒的水化。小疏水物水化自由能的温度依赖性的模型预测与实验一致。和简单分子溶质水合的模拟数据。提出了疏水水化从小到大的跨接长度尺度的三个替代定义,并获得了它们的温度依赖性。取决于定义和温度,预计从1到几纳米的半径的疏水物会发生水化机理中的小到大交叉。独立于其定义,预计交叉长度尺度将随温度升高而减小。

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