首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Rotational Diffusion of Charged and Nondipolar Solutes in Ionic Liquid-Organic Solvent Mixtures: Evidence for Stronger Specific Solute-Solvent Interactions in Presence of Organic Solvent
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Rotational Diffusion of Charged and Nondipolar Solutes in Ionic Liquid-Organic Solvent Mixtures: Evidence for Stronger Specific Solute-Solvent Interactions in Presence of Organic Solvent

机译:离子液体-有机溶剂混合物中带电和非偶极溶质的旋转扩散:在有机溶剂存在下更强的比溶质与溶剂相互作用的证据

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摘要

Rotational diffusion of a charged solute, rhodamine 110 (R110), and a nondipolar solute, 2,5-dimethyl-1,4-dioxo-3,6-diphenylpyrrolo[3,4-c]-pyrrole (DMDPP), has been investigated in ionic liquids, 1-butyl-3methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIM][Tf2N]) and 1-butyl-3-methylimidazolium tris(pentafluoroethyl)trifluorophosphate ([BMIM][FAP]), with 0.8 mole fraction of dibenzyl ether (DBE). This study has been undertaken to find Out how specific interactions between the solute and the ionic liquid are affected upon dilution with a nondipolar solvent. It has been observed that at a given viscosity (eta) and temperature (T), the reorientation times of R110 increase by 40-60% in the ionic liquid-organic solvent mixtures compared to ones in the corresponding neat ionic liquids. In the case of DMDPP, the influence of DBE is less pronounced, and its reorientation times increase by 25-50% at a given eta/T. The addition of DBE weakens the numerous interactions prevailing between the cations and the anions of the ionic liquids, which results in stronger specific interactions between the solutes and the constituent ions, consequently leading to slower rotation of the
机译:带电荷的溶质若丹明110(R110)和非偶极溶质2,5-二甲基-1,4-二氧代-3,6-二苯基吡咯并[3,4-c]-吡咯(DMDPP)的旋转扩散在离子液体中研究了1-丁基-3甲基咪唑双(三氟甲基磺酰基)酰亚胺([BMIM] [Tf2N])和1-丁基-3-甲基咪唑三(五氟乙基)三氟磷酸酯([BMIM] [FAP]),摩尔分数为0.8二苄基醚(DBE)。进行了这项研究以发现溶质和离子液体之间的特定相互作用在用非偶极溶剂稀释后如何受到影响。已经观察到,在给定的粘度(η)和温度(T)下,与相应的纯离子液体相比,在离子液体-有机溶剂混合物中,R110的重取向时间增加了40-60%。在DMDPP的情况下,DBE的影响不太明显,在给定的eta / T下,其重新定向时间增加了25-50%。 DBE的添加削弱了阳离子与离子液体阴离子之间的大量相互作用,这导致溶质与组成离子之间更强的比相互作用,从而导致离子液体的旋转变慢。

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