Diversity Observed in the Nanostructure of Protic Ionic Liquids

被引:226
|
作者
Greaves, Tamar L. [1 ]
Kennedy, Danielle F. [1 ]
Mudie, Stephen T. [2 ]
Drummond, Calum J. [1 ,3 ]
机构
[1] CSIRO Mol & Hlth Technol, Clayton, Vic 3169, Australia
[2] Australian Synchrotron, Clayton, Vic 3169, Australia
[3] CSIRO Mat Sci & Engn, Clayton, Vic 3169, Australia
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2010年 / 114卷 / 31期
基金
澳大利亚研究理事会;
关键词
X-RAY-SCATTERING; PHYSICOCHEMICAL PROPERTIES; MOLECULAR-INTERACTIONS; ETHYLAMMONIUM NITRATE; MICELLE FORMATION; CARBOXYLIC-ACIDS; TEMPERATURE; DYNAMICS; ORGANIZATION; BEHAVIOR;
D O I
10.1021/jp103863z
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The nanostructure of a series of 20 protic ionic liquids (PILs) has been investigated using small- and wide-angle X-ray scattering (SAXS and WAXS). The PILs contained alkylammonium, dialkylammonium, trialkylammonium, and cyclic ammonium cations combined with organic or inorganic anions. The presence of hydroxyl and methoxy substituents on the alkyl chains of the cations was also explored Many of the PILs showed a nanostructure resulting from segregation of the polar and nonpolar components of the ionic liquid It was found that this segregation was enhanced for longer alkyl chains, with a corresponding increase in the length scale, whereas the presence of hydroxyl groups on the alkyl chains led to much less ordered liquids. The broad range of protic ionic liquids studied allowed several structure property relationships to be established. The solvophobic effect was shown to be dependent on the nanostructure of the PILs. These PILs support amphiphile self-assembly, and it was shown that the less structured PILs had more "water-like" behavior in the diversity of lyotropic liquid-crystal phases supported, and the thermal stability ranges for these phases
引用
收藏
页码:10022 / 10031
页数:10
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