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控制质子离子液体中的微妙能量平衡:色散力与氢键竞争。

Controlling the subtle energy balance in protic ionic liquids: dispersion forces compete with hydrogen bonds.

机构信息

Universität Rostock, Institut für Chemie, Abteilung für Physikalische Chemie, Dr.-Lorenz-Weg 1, 18059, Rostock (Germany).

出版信息

Angew Chem Int Ed Engl. 2015 Feb 23;54(9):2792-5. doi: 10.1002/anie.201411509. Epub 2015 Jan 13.

Abstract

The properties of ionic liquids are determined by the energy-balance between Coulomb-interaction, hydrogen-bonding, and dispersion forces. Out of a set of protic ionic liquids (PILs), including trialkylammonium cations and methylsulfonate and triflate anions we could detect the transfer from hydrogen-bonding to dispersion-dominated interaction between cation and anion in the PIL [(C6 H13 )3 NH][CF3 SO3 ]. The characteristic vibrational features for both ion-pair species can be detected and assigned in the far-infrared spectra. Our approach gives direct access to the relative strength of hydrogen-bonding and dispersion forces in a Coulomb-dominated system. Dispersion-corrected density functional theory (DFT) calculations support the experimental findings. The dispersion forces could be quantified to contribute about 2.3 kJ mol(-1) per additional methylene group in the alkyl chains of the ammonium cation.

摘要

离子液体的性质取决于库仑相互作用、氢键和色散力之间的能量平衡。在一组质子离子液体(PILs)中,包括三烷基铵阳离子和甲基磺酸盐和三氟甲磺酸盐阴离子,我们可以检测到 PIL[(C6H13)3NH][CF3SO3]中阳离子和阴离子之间从氢键到色散力主导相互作用的转变。在远红外光谱中可以检测到并分配这两种离子对物种的特征振动特征。我们的方法可以直接测量在库仑主导体系中氢键和色散力的相对强度。经色散校正的密度泛函理论(DFT)计算支持实验结果。色散力可以量化为铵阳离子烷基链中每增加一个亚甲基贡献约 2.3 kJ/mol。

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