羟基功能化离子液体中的氢键基序。

IF 11.7 1区 化学 Q1 CHEMISTRY, PHYSICAL
Anne Strate, Dietmar Paschek, Ralf Ludwig
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引用次数: 0

摘要

离子液体的独特性质源于其组成离子之间的库仑相互作用、氢键和色散相互作用的可调范围。在羟基功能化的il中,局部和定向氢键(h键)导致预期的离子对的形成,但也导致难以捉摸的阳离子团簇的形成。在这里,我们回顾了氢键基序在羟基功能化il的液相和气相中如何揭示氢键的一般性质。红外光谱、核磁共振、中子衍射和分子动力学模拟提供了关于散装液体离子离子中阳离子团簇的结构、强度和动力学的信息。低温离子振动预解(CIVP)光谱和密度泛函理论计算已经建立了一个清晰的图像,在气相形成的孤立的h键阳离子团簇内的特定接触。这些来自实验、模拟和理论的信息提供了对离子间氢键的基本理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydrogen-Bonding Motifs in Hydroxy-Functionalized Ionic Liquids.

The unique properties of ionic liquids (ILs) result from the tunable mélange of Coulomb interactions, hydrogen bonding, and dispersion interactions among the constituent ions. In hydroxy-functionalized ILs, local and directional hydrogen bonds (H-bonds) lead to the anticipated formation of ion pairs but also to the elusive formation of cationic clusters. Here, we review how hydrogen-bonding motifs in the bulk liquid and gas phase of hydroxy-functionalized ILs shed light on the general nature of hydrogen bonding. Infrared spectroscopy, nuclear magnetic resonance, neutron diffraction, and molecular dynamics simulations provide information about the structure, strength, and dynamics of cationic clusters in the bulk liquid ILs. Cryogenic ion vibrational predissociation (CIVP) spectroscopy along with density functional theory calculations has established a clear picture about the specific contacts within isolated H-bonded cationic clusters formed in the gas phase. This information from experiment, simulation, and theory provides a fundamental understanding of hydrogen bonding between the ions in ILs.

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来源期刊
CiteScore
28.00
自引率
0.00%
发文量
21
期刊介绍: The Annual Review of Physical Chemistry has been published since 1950 and is a comprehensive resource for significant advancements in the field. It encompasses various sub-disciplines such as biophysical chemistry, chemical kinetics, colloids, electrochemistry, geochemistry and cosmochemistry, chemistry of the atmosphere and climate, laser chemistry and ultrafast processes, the liquid state, magnetic resonance, physical organic chemistry, polymers and macromolecules, and others.
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