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溶质与水的相互作用:多羟基化合物会改变水的性质吗?

Solute--water interactions: do polyhydroxy compounds after the properties of water?

作者信息

Franks F

出版信息

Cryobiology. 1983 Jun;20(3):335-45. doi: 10.1016/0011-2240(83)90022-6.

DOI:10.1016/0011-2240(83)90022-6
PMID:6884075
Abstract

The interactions between PHCs and water, like those between water molecules, are governed by hydrogen bonding. The details of these interactions are very sensitive to spacings and orientations of the -OH groups on the solute molecules. Where different conformers can coexist in solution, the aqueous solvent acts so as to favor the conformer with the largest number of equatorial -OH groups, because of their spatial compatibility with water. Because of this compatibility, aqueous solutions of PHCs have the tendency to supersaturation and incomplete freezing, manifestations of the phenomenon known as bound water which is, however, a misnomer. The range of water structure perturbation is probably governed by hydration forces which appear to dominate at solute-solute distances of less than 3 nm and which decay exponentially. Although on a single hydrogen bond basis the hydration effects are marginal, they nevertheless are responsible for many macroscopic phenomena, e.g., gel formation, liquid crystals, and protection against dehydration.

摘要

初级羟基化合物(PHCs)与水之间的相互作用,如同水分子之间的相互作用一样,受氢键支配。这些相互作用的细节对溶质分子上 -OH 基团的间距和取向非常敏感。在溶液中不同构象可以共存的情况下,水溶剂的作用是有利于具有最多赤道面 -OH 基团的构象,这是因为它们与水在空间上具有相容性。由于这种相容性,PHCs 的水溶液有过饱和和不完全冻结的倾向,这是被称为结合水现象的表现,然而这是一个误称。水结构扰动的范围可能受水化力支配,水化力似乎在溶质 - 溶质距离小于 3 nm 时起主导作用,并且呈指数衰减。尽管基于单个氢键而言,水化效应微不足道,但它们仍然导致了许多宏观现象,例如凝胶形成、液晶以及防止脱水。

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