2012
DOI: 10.1039/c2ra21772d
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What causes the low viscosity of ether-functionalized ionic liquids? Its dependence on the increase of free volume

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Cited by 108 publications
(129 citation statements)
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“…All these imidazolium-based materials including the imidazolium chloride salts and the imidazolium tetrachloroaluminates displayed the same order of magnitudes of ionic conductivities in mesophase, but the conductivity in isotropic phase was a magnitude greater or more than that in mesophase due to decrease of viscosity [48]. In comparison with the imidazolium chloride salts, the imidazolium tetrachloroaluminates presented a higher conductivity increase both in mesophase and in isotropic phase due to stronger interaction among AlCl 4 À and imidazolium cations, although very little difference in conductivity was observed in the imidazolium-based salts with the same anions.…”
Section: Conductivities Of the Imidazolium-based Lc Materialsmentioning
confidence: 90%
“…All these imidazolium-based materials including the imidazolium chloride salts and the imidazolium tetrachloroaluminates displayed the same order of magnitudes of ionic conductivities in mesophase, but the conductivity in isotropic phase was a magnitude greater or more than that in mesophase due to decrease of viscosity [48]. In comparison with the imidazolium chloride salts, the imidazolium tetrachloroaluminates presented a higher conductivity increase both in mesophase and in isotropic phase due to stronger interaction among AlCl 4 À and imidazolium cations, although very little difference in conductivity was observed in the imidazolium-based salts with the same anions.…”
Section: Conductivities Of the Imidazolium-based Lc Materialsmentioning
confidence: 90%
“…Ruiz et al demonstrated that the conductivity of 1-butyl-1-methylpyrrolidinium bis{(trifluoromethyl)sulfonyl}imide ([Pyrr 14 ][TFSI]) could be increased significantly from 2.5 mS · cm À1 to 45 mS · cm À1 at 25 8C by mixing the IL with acetonitrile. [11] The substitution of alkyl groups with a similarly sized, flexible ether group onto the cation structure has been shown previously to reduce the viscosity of the IL. [11] The substitution of alkyl groups with a similarly sized, flexible ether group onto the cation structure has been shown previously to reduce the viscosity of the IL.…”
Section: Introductionmentioning
confidence: 93%
“…This trend is observable in imidazolium, [45] ammonium, [46] sulfonium, [25] phosphonium, [47] and pyrazolium [15] ILs reported in the literature. These reduction in viscosities may be attributed to the increased flexibility of the cation chain, [11,12] or a reduction in inter-cationic association of the ethereal groups relative to the similarly sized alkyl groups. [46] Increasing the length of the alkyl chain (i. there is a balance on the resulting IL transport properties between the relative increase in cation size (molecular weight) and the promotional effects of introducing higher degrees of ether functionality.…”
Section: Viscositymentioning
confidence: 99%
“…Replacing an alkyl chain by an alkoxy chain in the IL cation shows a significant effect on the electrolyte viscosity (η) (Table ). Zheng et al . measured these to be highly variable and strongly dependent on the structures of the cation and ether moiety.…”
Section: Examples Of Ils and Pilsmentioning
confidence: 99%