Yalcin Dilek, Christofferson Andrew J, Drummond Calum J, Greaves Tamar L
School of Science, College of Science, Engineering and Health, RMIT University, GPO Box 2476, Melbourne, Victoria 3001, Australia.
Phys Chem Chem Phys. 2020 May 21;22(19):10995-11011. doi: 10.1039/d0cp00201a. Epub 2020 May 5.
Ionic liquids (ILs) are increasingly receiving interest for a wide range of applications. However, for many applications their cost and/or viscosity can be too high. This can be addressed by using protic ionic liquids as cheaper alternatives, and through mixing with molecular solvents. However, mixing ILs with a molecular solvent adds another dimension to the compositional space, as well as increasing the complexity of solvent-solute interactions. In this study, we have investigated the solvation properties of binary mixtures of PILs with molecular solvents. The selected binary solvent systems are the PILs ethylammonium nitrate (EAN) and propylammonium nitrate (PAN) combined with either water, methanol, acetonitrile or DMSO. In addition, water is combined with the other molecular solvents for comparison. The mole fractions of the secondary solvents were 0, 0.25, 0.5, 0.75, 0.9 and 1 for all combinations, which resulted in a total of 66 solvent mixtures. The solvation properties in each of these mixtures were determined from spectroscopic measurements of 4 well-known solvatochromic probe molecules as solutes. The solvation properties were comparatively investigated, and interpreted, in terms of the specific and non-specific interactions between PIL-solvent, PIL-solute and solvent-solute. All 66 solvent mixtures were also analysed using FTIR with no probe molecules present. In addition, through molecular dynamics simulations, the dye-solvent interactions were simulated for two of the dye molecules in water-EAN binary systems, and the radial distribution functions for the key interactions were obtained. The results showed that the solvation parameters of the binary mixtures deviated considerably from the ideal solvation behaviour. In many cases, bulk compositions and the estimated excess compositions in the solvation shells of the probes were different, suggesting preferential solvation, the extent of which is solute dependent. Our results clearly show that using PILs in a mixture with molecular solvents can strongly enhance the solvation capability.
离子液体(ILs)在广泛的应用中越来越受到关注。然而,对于许多应用来说,它们的成本和/或粘度可能过高。这可以通过使用质子离子液体作为更便宜的替代品,以及与分子溶剂混合来解决。然而,将离子液体与分子溶剂混合会给组成空间增加另一个维度,同时也增加了溶剂 - 溶质相互作用的复杂性。在本研究中,我们研究了质子离子液体与分子溶剂二元混合物的溶剂化性质。所选的二元溶剂体系是硝酸乙铵(EAN)和硝酸丙铵(PAN)这两种质子离子液体,它们分别与水、甲醇、乙腈或二甲基亚砜(DMSO)混合。此外,将水与其他分子溶剂混合进行比较。对于所有组合,第二溶剂的摩尔分数分别为0、0.25、0.5、0.75、0.9和1,这总共产生了66种溶剂混合物。这些混合物中每种的溶剂化性质是通过对4种著名的溶剂显色探针分子作为溶质进行光谱测量来确定的。从质子离子液体 - 溶剂、质子离子液体 - 溶质和溶剂 - 溶质之间的特异性和非特异性相互作用方面,对溶剂化性质进行了比较研究和解释。所有66种溶剂混合物在不存在探针分子的情况下也使用傅里叶变换红外光谱(FTIR)进行了分析。此外,通过分子动力学模拟,对水 - EAN二元体系中的两种染料分子的染料 - 溶剂相互作用进行了模拟,并获得了关键相互作用的径向分布函数。结果表明,二元混合物的溶剂化参数与理想溶剂化行为有很大偏差。在许多情况下,本体组成和探针溶剂化壳层中估计的过量组成不同,表明存在优先溶剂化,其程度取决于溶质。我们的结果清楚地表明,将质子离子液体与分子溶剂混合使用可以显著提高溶剂化能力。