Faculty of Chemistry and Chemical Technology, University of Ljubljana , SI-1000 Ljubljana, Slovenia.
J Phys Chem B. 2014 Feb 6;118(5):1426-35. doi: 10.1021/jp412344a. Epub 2014 Jan 24.
Molar conductivities, Λ, of dilute solutions of the ionic liquids (ILs) 1-ethyl-3-methylimidazolium tetrafluoroborate ([emim][BF4]), 1-butyl-3-methylimidazolium tetrafluoroborate ([bmim][BF4]), 1-butyl-3-methylimidazolium hexafluorophosphate ([bmim][PF6]), 1-hexyl-3-methylimidazolium tetrafluoroborate ([hmim][BF4]), and 1-hexyl-3-methylimidazolium bis-(trifluoromethanesulfonyl)amide ([hmim][NTf2]) in acetonitrile (AN) were determined as a function of temperature in the range 273.15-313.15 K. The data were analyzed with Barthel’s lcCM model to obtain limiting molar conductivities, Λ(∞)(T), and association constants, K(A)°(T) of these electrolytes. The temperature dependence of these parameters, as well as the extracted limiting cation conductivities, λ(i)(∞), were discussed. Additionally, dielectric spectra for [hmim][NTf2] + AN were analyzed in terms of ion association and ion solvation and compared with the inference from conductivity. It appears that in dilute solutions the imidazolium ring of the cations is solvated by ∼6 AN molecules that are slowed by a factor of ∼8-10 compared to the bulk-solvent dynamics. Ion association of imidazolium ILs to contact ion pairs is only moderate, similar to common 1:1 electrolytes in this solvent.
在 273.15-313.15 K 的温度范围内,测定了离子液体 1-乙基-3-甲基咪唑四氟硼酸盐([emim][BF4])、1-丁基-3-甲基咪唑四氟硼酸盐([bmim][BF4])、1-丁基-3-甲基咪唑六氟磷酸盐([bmim][PF6])、1-己基-3-甲基咪唑四氟硼酸盐([hmim][BF4])和 1-己基-3-甲基咪唑双(三氟甲烷磺酰基)酰胺([hmim][NTf2])在乙腈(AN)中的稀溶液摩尔电导率 Λ 随温度的变化。用 Barthel 的 lcCM 模型对数据进行了分析,得到了这些电解质的极限摩尔电导率 Λ(∞)(T)和缔合常数 K(A)°(T)。讨论了这些参数的温度依赖性,以及提取的极限阳离子电导率 λ(i)(∞)。此外,还根据离子缔合和离子溶剂化对 [hmim][NTf2]+AN 的介电谱进行了分析,并与电导率的推断进行了比较。在稀溶液中,阳离子的咪唑环似乎被 ∼6 个 AN 分子溶剂化,与本体溶剂动力学相比,这些分子的速度减慢了 ∼8-10 倍。离子液体的离子缔合作用仅为中等程度,与该溶剂中的常见 1:1 电解质相似。