Cation Alkyl Side Chain Length and Symmetry Effects on the Surface Tension of Ionic Liquids

被引:83
|
作者
Almeida, Hugo F. D. [1 ]
Freire, Mara G. [1 ]
Fernandes, Ana M. [2 ]
Lopes-da-Silva, Jose A. [2 ]
Morgado, Pedro [3 ]
Shimizu, Karina [3 ]
Filipe, Eduardo J. M. [3 ]
Canongia Lopes, Jose N. [3 ,4 ]
Santos, Luis M. N. B. F. [5 ]
Coutinho, Joao A. P. [1 ]
机构
[1] Univ Aveiro, Dept Quim, CICECO, P-3810193 Aveiro, Portugal
[2] Univ Aveiro, Dept Quim, QOPNA Unit, P-3810193 Aveiro, Portugal
[3] Univ Lisbon, Inst Super Tecn, Ctr Quim Estrutural, P-1049001 Lisbon, Portugal
[4] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2750154 Oeiras, Portugal
[5] Univ Porto, Fac Ciencias, Dept Quim & Bioquim, Ctr Invest Quim, P-4169007 Oporto, Portugal
关键词
MOLECULAR-FORCE FIELD; PHYSICAL-PROPERTIES; THERMODYNAMIC PROPERTIES; REFRACTIVE-INDEX; TEMPERATURE; DENSITY; ANION; WATER; PRESSURE; SOLUBILITY;
D O I
10.1021/la501308q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aiming at providing a comprehensive study of the influence of the cation symmetry and alkyl side chain length on the surface tension and surface organization of ionic liquids (ILs), this work addresses the experimental measurements of the surface tension of two extended series of ILs, namely R,R'-dialkylimidazolium bis-Rtrifluoromethyl)sulfonyllimide ([C(n)C(n)im][NTf2]) and R-alkyl-3-methylimidazolium bis[ (trifluoromethyl)sulfonyl] imide ([C-n C(1)im]-[NTf2D, and their dependence with temperature (from 298 to 343 K). For both series of ILs the surface tension decreases with an increase in the cation side alkyl chain length up to aliphatic chains no longer than hexyl, here labeled as critical alkyl chain length (CACL). For ILs with aliphatic moieties longer than CACL the surface tension displays an almost constant value up to [C(12)C(1)im][NTf2] or [C(16)C(1)im][NTf2]. These constant values further converge to the surface tension of long chain n-alkanes, indicating that, for sufficiently long alkyl side chains, the surface ordering is strongly dominated by the aliphatic tails present in the IL. The enthalpies and entropies of surface were also derived and the critical temperatures were estimated from the experimental data. The trend of the derived thermodynamic Properties highlights the effect of the structural organization of the IL at the surface with visible trend shifts occurring at a well-defined CACL in both symmetric and asymmetric series of ILs. Finally, the structure of a long-alkyl side chain IL at the vacuum-liquid interface was also explored using Molecular Dynamics simulations. In general, it was found that for the symmetric series of ILs, at the outermost polar layers, more cations point one of their aliphatic tails outward and the other inward, relative to the surface, than cations pointing both tails outward. The number of the former, while being the preferred conformation, exceeds the latter by around 75%.
引用
收藏
页码:6408 / 6418
页数:11
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