School of Chemistry, Monash University, 17 Rainforest Walk, Clayton, VIC 3800, Australia.
Department of Pathophysiology, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan.
J Phys Chem B. 2020 Oct 15;124(41):9182-9194. doi: 10.1021/acs.jpcb.0c07732. Epub 2020 Oct 2.
Ionic liquids (ILs) such as choline dihydrogen phosphate exhibit an extraordinary solubilizing ability for proteins such as cytochrome C when mixed with 20 wt % water. Most widely used imidazolium-based ionic liquids coupled with dihydrogen phosphate do not exhibit the same solubilizing properties, suggesting that a multifunctional cation such as choline might play a key role in enhancing these properties of ionic liquid mixtures with water. In this theoretical work, we compare intermolecular interactions between the water molecule and ionic liquid ions in two ion-paired clusters of choline- and 1-butyl-3-methyl-imidazolium-based ionic liquids coupled with acetate, dihydrogen phosphate, and mesylate. Gibbs free energy (GFE) of solvation of water in these ionic liquids was calculated. Incorporation of a water molecule into ionic liquid clusters was accompanied by negative GFEs of solvation in both types of cations. These results were in good agreement with previously reported experimental GFEs of solvation of water in ILs. Compared to imidazolium-based clusters, strong interionic interactions of choline ionic liquids resulted in more negative GFEs due to their smaller deformation upon the addition of a water molecule, with dihydrogen phosphate and mesylate predicting the lowest GFEs of -30.1 and -43.5 kJ/mol, respectively. Lower GFEs of solvation of water in choline-based clusters were also accompanied with smaller entropic penalties, suggesting that water easily incorporates itself into the existing ionic network. Analysis of the intramolecular bonds within the water molecule showed that the choline hydroxyl group donates electron density to the neighboring water molecule, leading to additional polarization. The predicted infrared spectra of clusters of ionic liquids with water showed a pronounced red shift due to strongly polarized O-H bonds, in excellent agreement with the experimentally measured infrared spectra of ionic liquid mixtures with water. Increased polarization of water in choline-based ionic liquids undoubtedly creates more effective solvents for stabilizing biological molecules such as proteins.
离子液体(ILs),如磷酸二氢胆碱,当与 20wt%的水混合时,对细胞色素 C 等蛋白质表现出非凡的溶解能力。最广泛使用的基于咪唑的离子液体与磷酸二氢结合时,并不表现出相同的溶解特性,这表明多功能阳离子,如胆碱,可能在增强离子液体与水混合物的这些特性方面发挥关键作用。在这项理论工作中,我们比较了水和离子液体离子在两个离子对簇之间的分子间相互作用,这两个离子对簇由胆碱和 1-丁基-3-甲基咪唑鎓基离子液体与醋酸盐、磷酸二氢和甲磺酸盐偶联而成。计算了这些离子液体中水的溶剂化吉布斯自由能(GFE)。在这两种阳离子中,水分子掺入离子液体簇伴随着溶剂化的负 GFE。这些结果与之前报道的离子液体中水的实验 GFE 吻合较好。与基于咪唑的簇相比,胆碱离子液体的强离子间相互作用导致更负的 GFE,因为它们在加入水分子时的变形较小,磷酸二氢和甲磺酸盐分别预测出最低的 GFE 值为-30.1 和-43.5kJ/mol。胆碱基簇中水的溶剂化更低的 GFE 也伴随着较小的熵罚,这表明水很容易融入现有的离子网络。对水分子内分子键的分析表明,胆碱羟基基团向相邻水分子提供电子密度,导致额外的极化。离子液体与水的簇的预测红外光谱由于强烈极化的 O-H 键而显示出明显的红移,与离子液体与水的混合物的实验测量的红外光谱非常吻合。胆碱基离子液体中水的极化增加无疑为稳定蛋白质等生物分子创造了更有效的溶剂。