Structure and Orientation of the Imidazolium Cation at the Room-Temperature Ionic Liquid/SiO2Interface Measured by Sum-Frequency Vibrational Spectroscopy†

2007 ◽  
Vol 111 (18) ◽  
pp. 4990-4999 ◽  
Author(s):  
Julie B. Rollins ◽  
Brian D. Fitchett ◽  
John C. Conboy
2011 ◽  
Vol 306-307 ◽  
pp. 1693-1697
Author(s):  
Xiao Nan Li ◽  
Mei Shan Pei ◽  
Lu Yan Wang ◽  
Li Wang

Phase behavior of ternary systems involving PEO-PPO-PEO block copolymer (Pluronic P123), room-temperature ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate [Bmim]PF6, and glycerol is investigated at 25 °C by using small-angle X-ray scattering (SAXS) techniques. In this ternary system, the structures formed in the binary P123/[Bmim]PF6 system, hexagonal phase (H1) and lamellar phase (Lα), are still obtained. At lower P123/[Bmim]PF6 ratio, the H1 phase can accommodate more than 30 % glycerol. At higher P123/[Bmim]PF6 ratio, the Lα phase only accommodates less than 2 % glycerol and Lα changes to H1 with increasing the glycerol content. Moreover, a phase separation takes place at a higher glycerol content. Solvatophobic interactions between hydrophobic groups of [Bmim]PF6 and P123, coulombic force existing in the polyoxyethylene chain and imidazolium cation, H-bond between P123 and glycerol, accompanying with the force ascribe to the nitrogen of the imidazole ring and the oxygen of alcohol are helpful for the formation of long-range ordered structure.


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