Solute–solvent hydrogen-bonding in room temperature ionic liquids studied by Raman spectroscopy

2012 ◽  
Vol 14 (39) ◽  
pp. 13676 ◽  
Author(s):  
Akira Kobayashi ◽  
Koji Osawa ◽  
Masahide Terazima ◽  
Yoshifumi Kimura

2007 ◽  
Vol 111 (45) ◽  
pp. 13028-13032 ◽  
Author(s):  
Yasuhiro Umebayashi ◽  
Takushi Mitsugi ◽  
Shuhei Fukuda ◽  
Takao Fujimori ◽  
Kenta Fujii ◽  
...  




2002 ◽  
Vol 4 (5) ◽  
pp. 517-520 ◽  
Author(s):  
Ajay Aggarwal ◽  
N. Llewellyn Lancaster ◽  
Alick R. Sethi ◽  
Tom Welton


Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 355
Author(s):  
Fabricio R. Bisogno ◽  
Rosario Fernández ◽  
Jose María Lassaletta ◽  
Gonzalo de de Gonzalo

Room temperature ionic liquids (RTILs) have been widely used as (co)solvents in several catalytic processes modifying, in most of the cases, the catalyst activity and/or the selectivity for the studied reactions. However, there are just a few examples of their use in hydrogen bonding organocatalysis. In this paper, we show the positive effect of a set of imidazole-based ionic liquids ([bmim]BF4 and [hmim]PF6) in the enantioselective addition of formaldehyde tert-butylhydrazone to prochiral α-keto esters catalyzed by a sugar-based chiral thiourea. Reactions performed in the presence of low percentages of RTILs led to an increase of the catalyst activity, thereby making possible to work at lower temperatures. Thus, the chiral tert-butyl azomethyl tertiary alcohols could be obtained with moderate to good conversions and higher enantioselectivities for most of the studied substrates when using up to 30 vol% of [hmim]PF6 as a cosolvent in processes performed in toluene.





2013 ◽  
Vol 42 (1) ◽  
pp. 63-65 ◽  
Author(s):  
Rong Lu ◽  
Wei Wang ◽  
Shuwei Yuan ◽  
Anchi Yu


2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Naohiro Hatano ◽  
Takahiro Takekiyo ◽  
Hiroshi Abe ◽  
Yukihiro Yoshimura

We have investigated the nonspherical anion effect on the trans-trans (TT) and gauche-trans (GT) equilibrium in pure 1-butyl-3-methylimidazolium ([bmim]+)-based room temperature ionic liquids (RTILs) by the Raman spectroscopy. The intensity ratio of the [bmim]+ cation in [bmim]+-based RTILs having nonspherical anions changes with nature of the anions. However, the enthalpy change of the [bmim]+ cation is approximately −1.0 kJ/mol for all [bmim]+-based RTILs used in this study and is independent of the anionic species. The present results indicate that the conformational stability of the [bmim]+ cation in [bmim]+-based RTILs including nonspherical anions is driven by the entropic contribution associated with the orientation and configuration of the [bmim]+ cation with respect to the counteranion.



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