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水在不同组成的水再矿化混合物中的微观结构特征。

Microscopic structural features of water in aqueous-reline mixtures of varying compositions.

机构信息

Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai 400076, India.

出版信息

Phys Chem Chem Phys. 2021 Feb 14;23(6):3779-3793. doi: 10.1039/d0cp05341d. Epub 2021 Feb 3.

Abstract

Reline, a mixture of urea and choline chloride in a 2 : 1 molar ratio, is one of the most frequently used deep eutectic solvents. Pure reline and its aqueous solution have large scale industrial use. Owing to the presence of active hydrogen bond formation sites, urea and choline cations can disrupt the hydrogen-bonded network in water. However, a quantitative understanding of the microscopic structural features of water in the presence of reline is still lacking. We carry out extensive all-atom molecular dynamics simulations to elucidate the effect of the gradual addition of co-solvents on the microscopic arrangements of water molecules. We consider four aqueous solutions of reline, between 26.3 and 91.4 wt%. A disruption of the local hydrogen-bonded structure in water is observed upon inclusion of urea and choline chloride. The extent of deviation of the water structure from tetrahedrality is quantified using the tetrahedral order parameter (q). Our analyses show a monotonic increase in the structural disorder as the co-solvents are added. Increase in the q values are observed when highly electro-negative hetero-atoms like nitrogen, oxygen of urea and choline cations are counted as partners of the central water molecules. Further insights are drawn from the characterization of the hydrogen-bonded network in water and we observe the gradual rupturing of water-water hydrogen bonds and their subsequent replacement by the water-urea hydrogen bonds. A negligible contribution from the hydrogen bonds between water and bulky choline cations has also been found. Considering all the constituents as the hydrogen bond partners we calculate the possibility of a successful hydrogen bond formation with a central water molecule. This gives a clear picture of the underlying mechanism of water replacement by urea.

摘要

复配,即尿素和氯化胆碱摩尔比为 2:1 的混合物,是最常使用的深共熔溶剂之一。纯复配及其水溶液具有大规模的工业用途。由于存在形成氢键的活性氢原子键合位点,尿素和胆碱阳离子可以破坏水中的氢键网络。然而,对于复配存在时水中微观结构特征的定量理解仍然缺乏。我们进行了广泛的全原子分子动力学模拟,以阐明共溶剂逐渐添加对水分子微观排列的影响。我们考虑了四种浓度在 26.3 至 91.4wt%之间的复配水溶液。当加入尿素和氯化胆碱时,观察到水中局部氢键结构的破坏。通过使用四面体有序参数(q)来量化水分子结构偏离四面体的程度。我们的分析表明,随着共溶剂的加入,结构无序度呈单调增加。当将尿素和胆碱阳离子中的高电负性杂原子(如氮、氧)计为中心水分子的配体时,q 值会增加。通过对水中氢键网络的特征进行进一步分析,我们观察到水-水氢键逐渐断裂,并被水-尿素氢键取代。还发现水与庞大的胆碱阳离子之间的氢键几乎没有贡献。考虑所有成分作为氢键配体,我们计算了与中心水分子形成氢键的可能性。这清楚地说明了尿素取代水的潜在机制。

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