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水分子超分子聚集体中氢键模式的热力学

Thermodynamics of hydrogen bond patterns in supramolecular assemblies of water molecules.

作者信息

Henry Marc

机构信息

Solid-State Molecular Tectonics Institut Le Bel Université Louis Pasteur 4, Rue Blaise Pascal, 67070 Strasbourg, France.

出版信息

Chemphyschem. 2002 Jul 2;3(7):607-16. doi: 10.1002/1439-7641(20020715)3:7<607::AID-CPHC607>3.0.CO;2-A.

DOI:10.1002/1439-7641(20020715)3:7<607::AID-CPHC607>3.0.CO;2-A
PMID:12503162
Abstract

The PACHA (Partial Atomic Charges and Hardnesses Analysis) formalism is applied to various supramolecular assemblies of water molecules. After a detailed study of all available crystal structures for ice polymorphs, we shown that the hydrogen bond strength is roughly constant below 1 GPa and considerably weakened above that value. New hydrogen bond patterns are proposed for ice IV, V, and VI after (EB) (electrostatic balance) minimization. For other polymorphs, there is an almost perfect coincidence between experimental and predicted hydrogen bond patterns. The evolution of hydrogen bond energy as a function of molecular geometry in water clusters with up to 280 water molecules and in large supramolecular compounds is quantitatively described. Intermolecular hydrogen bonds are found to lie between -9 and -32 kJ mol-1, the stronger interaction occurs within the spherical fully disordered water droplet buried at the heart of Müller's superfullerene keplerate. The weakest one occurs in a chiral molecular snub cube built from six calix[4]resorcinarene and eight water molecules. Intramolecular hydrogen bonds are found in the range -10-100 kJ mol-1 and can thus be considerably stronger than intermolecular bonds. Finally, through the investigation of a clathrate type I compound, it was possible to obtain a deep insight of the host-guest interactions and self-assembly rules of water cages in these materials.

摘要

PACHA(部分原子电荷与硬度分析)形式体系被应用于水分子的各种超分子聚集体。在对冰多晶型物的所有可用晶体结构进行详细研究之后,我们表明氢键强度在1吉帕以下大致恒定,而在该值以上则显著减弱。在(EB)(静电平衡)最小化之后,为冰IV、V和VI提出了新的氢键模式。对于其他多晶型物,实验和预测的氢键模式几乎完全吻合。定量描述了氢键能量随分子几何结构在含有多达280个水分子的水簇以及大型超分子化合物中的变化。发现分子间氢键介于-9至-32千焦每摩尔之间,较强的相互作用发生在埋于米勒超富勒烯开普勒笼核心的球形完全无序水滴内部。最弱的氢键出现在由六个杯[4]间苯二酚芳烃和八个水分子构成的手性分子截顶立方体中。分子内氢键的能量范围在-10至100千焦每摩尔之间,因此可能比分子间键强得多。最后,通过对一种I型包合物的研究,得以深入了解这些材料中水笼的主客体相互作用和自组装规则。

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