羟基氢键网络中相互作用几何与协同性的关系

IF 7.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Lucia Trevisan, Andrew D. Bond and Christopher A. Hunter
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引用次数: 0

摘要

氢键网络中相互作用之间的协同性可以使含有羟基的氢键的强度增加多达50%。通过比较一系列羟基甲酚和相应系列双酚的氢键性质,量化了改变分子内羟基-羟基氢键的几何形状对分子间羟基·喹啉氢键的协同性的影响。在羟基甲酚中,分子内氢键形成一个6元环,x射线晶体学显示,氢键从理想的线性O - h⋯O几何形状扭曲了35°。在双酚类化合物中,分子内氢键形成一个8元环,其几何结构接近理想,供体的氢键直接指向受体的孤对。用核磁共振氢谱法证实了溶液中分子内氢键相互作用的存在,并用核磁共振滴定法测定了与喹啉在正辛烷中形成1:1配合物的缔合常数。与苯甲醇与喹啉形成的非配合氢键相比,羟基甲酚形成的分子间氢键强度增加了−8 ~−14 kJ mol−1,这取决于苯酚OH供体的取代基对。吸电子取代基使苯酚成为较好的氢键供体,分子内氢键强度的增加导致与喹啉分子间氢键强度的增加。对于双酚类,协同作用非常相似:取代基效应几乎相同,并且分子内氢键的存在使分子间相互作用的强度增加了−10 kJ mol−1至−16 kJ mol−1。结果表明,氢键网络的协同性很大程度上取决于相互作用基团的极性,而对精确的几何排列相对不敏感。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups†

Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups†

Relationship between interaction geometry and cooperativity measured in H-bonded networks of hydroxyl groups†

Cooperativity between interactions in H-bonded networks can increase the strengths of H-bonds involving hydroxyl groups by up to 50%. The effect of changing the geometry of an intramolecular hydroxyl–hydroxyl H-bond on cooperativity with an intermolecular hydroxyl·quinuclidine H-bond was quantified by comparing the H-bonding properties of a series of hydroxycresols with the corresponding series of bisphenols. In the hydroxycresols, the intramolecular H-bond forms a 6-membered ring, and X-ray crystallography showed that the H-bond is distorted away from the ideal linear O–H⋯O geometry by up to 35°. In the bisphenols, the intramolecular H-bond forms an 8-membered ring, and the geometry is close to ideal, with the OH bond of the donor pointing directly at the lone pair of the acceptor. The presence of the intramolecular H-bonding interactions in solution was confirmed using 1H NMR spectroscopy, and NMR titrations were used to measure the association constants for formation 1 : 1 complexes with quinuclidine in n-octane. Compared with the non-cooperative H-bond formed by benzyl alcohol with quinuclidine, the strength of the intermolecular H-bond formed by the hydroxycresols increased by between −8 kJ mol−1 and −14 kJ mol−1, depending on the substituent para to the phenol OH donor. Electron-withdrawing substituents make the phenol a better H-bond donor, and the increase in the strength of the intramolecular H-bond leads to an increase in the strength of the intermolecular H-bond with quinuclidine. For the bisphenols, the cooperative effects were very similar: the substituent effects were practically identical, and the presence of the intramolecular H-bond increased the strength of the intermolecular interaction by between −10 kJ mol−1 and −16 kJ mol−1. The results show that cooperativity in H-bonded networks depends strongly on the polarity of the interacting groups but is relatively insensitive to the precise geometric arrangement.

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来源期刊
Chemical Science
Chemical Science CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
14.40
自引率
4.80%
发文量
1352
审稿时长
2.1 months
期刊介绍: Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.
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