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Structure and dynamics of ionic liquids: Trimethylsilylpropyl-substituted cations and bis(sulfonyl)amide anions

机译:离子液体的结构和动力学:三甲基甲硅烷基丙基取代的阳离子和双(磺酰基)酰胺阴离子

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Ionic liquids with cationic organosilicon groups have been shownto have a number of useful properties, including reduced viscosities relative to the homologous cations with hydrocarbon substituents on the cations. We report structural and dynamical properties of four ionic liquids having a trimethylsilylpropyl functional group, including 1-methyl-3-trimethylsilylpropylimidazolium (Si-C-3-mim(+)) cation paired with three anions: bis(fluorosulfonyl)imide (FSI-), bis(trifluoromethanesulfonyl) imide (NTf-), and bis(pentafluoroethanesulfonyl) imide (BETI-), as well as the analogous N-methyl-N-trimethylsilylpropylpyrrolidinium (Si-C-3-pyrr(+)) cation paired with NTf-. This choice of ionic liquids permits us to systematically study how increasing the size and hydrophobicity of the anions affects the structural and transport properties of the liquid. Structure factors for the ionic liquids were measured using high energy X-ray diffraction and calculated from molecular dynamics simulations. The liquid structure factors reveal first sharp diffraction peaks (FSDPs) for each of the four ionic liquids studied. Interestingly, the domain size for Si-C-3-mim(+)/NTf2 indicated by the maxima for these peaks is larger than for the more polar ionic liquid with a similar chain length, 1-pentamethyldisiloxymethyl-3-methyl-imidazolium bis(trifluoromethanesulfonyl) imide (SiOSi-mim(+)/NTf2). For the series of Si-C3-mim+ ionic liquids, as the size of the anion increases, the position of FSDP indicates that the intermediate range order domains decrease in size, contrary to expectation. Diffusivities for the anions and cations are compared for a series of both hydrocarbon-substituted and silicon-substituted cations. All of the anions show the same scaling with temperature, size, and viscosity, while the cations show two distinct trends-one for hydrocarbon-substituted cations and another for organosilicon-substituted cations, with the latter displaying increased friction. Published by AIP Publishing.
机译:已显示具有阳离子有机硅基团的离子液体具有许多有用的性质,包括相对于在阳离子上具有烃取代基的同源阳离子而言,粘度降低。我们报告了具有三甲基甲硅烷基丙基官能团的四种离子液体的结构和动力学性质,包括与三个阴离子配对的1-甲基-3-三甲基甲硅烷基丙基咪唑鎓(Si-C-3-mim(+))阳离子:双(氟磺酰基)酰亚胺(FSI- ),双(三氟甲磺酰基)酰亚胺(NTf-)和双(五氟乙磺酰基)酰亚胺(BETI-)以及与之配对的类似N-甲基​​-N-三甲基甲硅烷基丙基吡咯烷鎓(Si-C-3-pyrr(+))阳离子NTf-。离子液体的选择使我们能够系统地研究增加阴离子的大小和疏水性如何影响液体的结构和传输性能。使用高能X射线衍射测量离子液体的结构因子,并根据分子动力学模拟进行计算。液体结构因子揭示了所研究的四种离子液体中的每一种的第一个尖锐的衍射峰(FSDP)。有趣的是,由这些峰的最大值表示的Si-C-3-mim(+)/ NTf2的畴尺寸大于具有相似链长的极性更强的离子液体1-戊二甲基二甲硅烷氧基甲基-3-甲基咪唑鎓双(三氟甲磺酰基)酰亚胺(SiOSi-mim(+)/ NTf2)。对于一系列Si-C3-mim +离子液体,随着阴离子尺寸的增加,FSDP的位置表明中间范围有序域的尺寸减小,这与预期相反。比较了一系列烃取代和硅取代阳离子的阴离子和阳离子的扩散率。所有阴离子在温度,尺寸和粘度上均显示相同的结垢,而阳离子则显示出两种不同的趋势,一种是烃取代的阳离子,另一种是有机硅取代的阳离子,后者表现出增加的摩擦力。由AIP Publishing发布。

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