A 1,2,3-triazolate lithium salt with ionic liquid properties at room temperature

2018 ◽  
Vol 54 (65) ◽  
pp. 9035-9038 ◽  
Author(s):  
D. Flachard ◽  
J. Rolland ◽  
M. M. Obadia ◽  
A. Serghei ◽  
R. Bouchet ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Room Temperature ◽  
Lithium Salt ◽  
Triethylene Glycol

A triethylene glycol-based 1,2,3-triazolate lithium salt with ionic liquid properties at room temperature is synthesized in three steps including copper-catalysed cycloaddition between alkyne-functionalized monomethoxy-triethylene glycol and azidomethyl pivalate, followed by the deprotection of the methyl pivalate group and further lithiation of the 1H-1,2,3-triazole intermediate.

Quaternary Ammonium Room-Temperature Ionic Liquid/Lithium Salt Binary Electrolytes: Electrochemical Study

2008 ◽  
Vol 155 (6) ◽  
pp. A421 ◽  
Author(s):  
Shiro Seki ◽  
Yasutaka Ohno ◽  
Hajime Miyashiro ◽  
Yo Kobayashi ◽  
Akira Usami ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Quaternary Ammonium ◽  
Room Temperature ◽  
Lithium Salt ◽  
Room Temperature Ionic Liquid ◽  
Electrochemical Study ◽  
Liquid Lithium

Spontaneous polyiodide formation by unbalancing of charge in room-temperature ionic liquid-lithium salt solutions

2018 ◽  
Vol 503 ◽  
pp. 25-30 ◽  
Author(s):  
Hiroaki Kishimura ◽  
Masami Aono ◽  
Yoshiki Kyuko ◽  
Shoki Nagaya ◽  
Shu Koyama ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Room Temperature ◽  
Lithium Salt ◽  
Room Temperature Ionic Liquid ◽  
Liquid Lithium ◽  
Salt Solutions

Room Temperature Ionic Liquid−Lithium Salt Mixtures: Optical Kerr Effect Dynamical Measurements

2010 ◽  
Vol 114 (25) ◽  
pp. 8350-8356 ◽  
Author(s):  
Bruno G. Nicolau ◽  
Adam Sturlaugson ◽  
Kendall Fruchey ◽  
Mauro C. C. Ribeiro ◽  
M. D. Fayer
Keyword(s):  
Ionic Liquid ◽  
Kerr Effect ◽  
Room Temperature ◽  
Lithium Salt ◽  
Room Temperature Ionic Liquid ◽  
Liquid Lithium ◽  
Optical Kerr Effect ◽  
Salt Mixtures

Preparation and Characterization of a Novel Room Temperature Dicationic Ionic Liquid and its Application in the Synthesis of Xanthenediones Under Solvent-Free Conditions

2018 ◽  
Vol 21 (8) ◽  
pp. 602-608 ◽  
Author(s):  
Zainab Ehsani-Nasab ◽  
Ali Ezabadi
Keyword(s):  
Ionic Liquid ◽  
Room Temperature ◽  
Reaction Times ◽  
Significant Loss ◽  
Solvent Free ◽  
Acidity Function ◽  
Efficient Catalyst ◽  
Solvent Free Conditions ◽  
Hammett Acidity Function ◽  
Dicationic Ionic Liquid

Aim and Objective: In the present work, 1, 1’-sulfinyldiethylammonium bis (hydrogen sulfate) as a novel room temperature dicationic ionic liquid was synthesized and used as a catalyst for xanthenediones synthesis. Material and Method: The dicationic ionic liquid has been synthesized using ethylamine and thionyl chloride as precursors. Then, by the reaction of [(EtNH2)2SO]Cl2 with H2SO4, [(EtNH2)2SO][HSO4]2 was prepared and after that, it was characterized by FT-IR, 1H NMR, 13C NMR as well as Hammett acidity function. This dicationic ionic liquid was used as a catalyst for the synthesis of xanthenediones via condensation of structurally diverse aldehydes and dimedone under solvent-free conditions. The progress of the reaction was monitored by thin layer chromatography (ethyl acetate/n-hexane = 3/7). Results: An efficient solvent-free method for the synthesis of xanthenediones has been developed in the presence of [(EtNH2)2SO][HSO4]2 as a powerful catalyst with high to excellent yields, and short reaction times. Additionally, recycling studies have demonstrated that the dicationic ionic liquid can be readily recovered and reused at least four times without significant loss of its catalytic activity. Conclusion: This new dicationic ionic liquid can act as a highly efficient catalyst for xanthenediones synthesis under solvent-free conditions.

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