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首页> 外文期刊>Angewandte Chemie >Controlling the Subtle Energy Balance in Protic Ionic Liquids: Dispersion Forces Compete with Hydrogen Bonds
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Controlling the Subtle Energy Balance in Protic Ionic Liquids: Dispersion Forces Compete with Hydrogen Bonds

机译:控制质子离子液体中的微妙能量平衡:色散力与氢键竞争

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摘要

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 [(C6H13)(3)NH][CF3SO3]. 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 2.3kJmol(-1) per additional methylene group in the alkyl chains of the ammonium cation.
机译:离子液体的性质取决于库仑相互作用,氢键和分散力之间的能量平衡。在一组质子离子液体(PIL)中,包括三烷基铵阳离子,甲基磺酸根和三氟甲磺酸根阴离子,我们可以检测PIL [(C6H13)(3)NH]中阳离子与阴离子之间从氢键转移到分散为主的相互作用的转移。 [CF3SO3]。两种离子对物质的特征振动特征都可以被检测到,并在远红外光谱中进行分配。我们的方法可以直接获得库仑控制系统中氢键和分散力的相对强度。色散校正的密度泛函理论(DFT)计算支持实验结果。可以对分散力进行定量,以使铵阳离子烷基链中每个额外的亚甲基贡献约2.3kJmol(-1)。

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