Suppr超能文献

与刚性溶质相互作用时的水排列:多构型葑酮 -(HO)水合物

Water Arrangements upon Interaction with a Rigid Solute: Multiconfigurational Fenchone-(HO) Hydrates.

作者信息

Burevschi Ecaterina, Chrayteh Mhamad, Murugachandran S Indira, Loru Donatella, Dréan Pascal, Sanz M Eugenia

机构信息

Department of Chemistry, King's College London, London SE1 1DB, U.K.

PhLAM─Physique des Lasers, Atomes et Molécules, University of Lille, CNRS, UMR 8523, F-59000 Lille, France.

出版信息

J Am Chem Soc. 2024 Apr 17;146(15):10925-10933. doi: 10.1021/jacs.4c01891. Epub 2024 Apr 8.

Abstract

Insight into the arrangements of water molecules around solutes is important to understand how solvation proceeds and to build reliable models to describe water-solute interactions. We report the stepwise solvation of fenchone, a biogenic ketone, with 4-7 water molecules. Multiple hydrates were observed using broadband rotational spectroscopy, and the configurations of four fenchone-(HO), three fenchone-(HO), two fenchone-(HO), and one fenchone-(HO) complexes were characterized from the analysis of their rotational spectra in combination with quantum-chemical calculations. Interactions with fenchone deeply perturb water configurations compared with the pure water tetramer and pentamer. In two fenchone-(HO) complexes, the water tetramer adopts completely new arrangements, and in fenchone-(HO), the water pentamer is no longer close to being planar. The water hexamer interacts with fenchone as the least abundant book isomer, while the water heptamer adopts a distorted prism structure, which forms a water cube when including the fenchone oxygen in the hydrogen bonding network. Differences in hydrogen bonding networks compared with those of pure water clusters show the influence of fenchone's topology. Specifically, all observed hydrates except one show two water molecules binding to fenchone through each oxygen lone pair. The observation of several water arrangements for fenchone-(HO) complexes highlights water adaptability and provides insight into the solvation process.

摘要

深入了解溶质周围水分子的排列对于理解溶剂化过程以及构建可靠模型来描述水 - 溶质相互作用至关重要。我们报告了冰片酮(一种生物源酮)与4 - 7个水分子的逐步溶剂化过程。使用宽带旋转光谱观察到了多种水合物,并通过结合量子化学计算对其旋转光谱进行分析,表征了四个冰片酮 -(H₂O)、三个冰片酮 -(H₂O)、两个冰片酮 -(H₂O)和一个冰片酮 -(H₂O)配合物的构型。与纯水四聚体和五聚体相比,与冰片酮的相互作用极大地扰乱了水的构型。在两个冰片酮 -(H₂O)配合物中,水四聚体采用了全新的排列方式,而在冰片酮 -(H₂O)中,水五聚体不再接近平面结构。水六聚体与冰片酮相互作用时呈现出最不常见的书页异构体,而水七聚体采用扭曲的棱柱结构,当在氢键网络中包含冰片酮的氧时会形成一个水立方。与纯水团簇相比,氢键网络的差异显示了冰片酮拓扑结构的影响。具体而言,除了一个之外,所有观察到的水合物都显示有两个水分子通过每个氧孤对与冰片酮结合。对冰片酮 -(H₂O)配合物几种水排列的观察突出了水的适应性,并为溶剂化过程提供了深入见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9042/11027134/a1e0acc80edf/ja4c01891_0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验