scholarly journals One-pot synthesis of symmetric imidazolium ionic liquids N,N-disubstituted with long alkyl chains

RSC Advances ◽  
2020 ◽  
Vol 10 (36) ◽  
pp. 21071-21081
Author(s):  
Giacomo Damilano ◽  
Demian Kalebić ◽  
Koen Binnemans ◽  
Wim Dehaen
Keyword(s):  
Ionic Liquids ◽  
High Yield ◽  
One Pot ◽  
Imidazolium Ionic Liquids ◽  
Alkyl Chains ◽  
One Pot Synthesis ◽  
Greener Synthesis ◽  
Long Chain

The modified Debus–Radziszewski reaction was used as a one-pot on-water reaction to allow a greener synthesis of long-chain 1,3-dialkylimidazolium acetate ionic liquids in high yield from long-chain linear amines.

Facile One-Pot Synthesis of 1-Alkyl-3-polyfluoroalkyl Imidazolium Ionic Liquids

Synlett ◽  
2009 ◽  
Vol 2009 (13) ◽  
pp. 2101-2104 ◽  
Author(s):  
Hoon Kim ◽  
Hyunjoo Lee ◽  
Dong Kim ◽  
Debby Natalia ◽  
Dihn Nguyen ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
One Pot ◽  
Imidazolium Ionic Liquids ◽  
One Pot Synthesis

ChemInform Abstract: Facile One-Pot Synthesis of 1-Alkyl-3-polyfluoroalkyl Imidazolium Ionic Liquids.

ChemInform ◽  
2009 ◽  
Vol 40 (52) ◽  
Author(s):  
Dong Sub Kim ◽  
Debby Natalia ◽  
Dihn Quan Nguyen ◽  
Dong Jin Suh ◽  
Honggon Kim ◽  
...  
Keyword(s):  
Ionic Liquids ◽  
One Pot ◽  
Imidazolium Ionic Liquids ◽  
One Pot Synthesis

Unexpected self-assembly, photoluminescence behavior, and film-forming properties of polysiloxane-based imidazolium ionic liquids prepared by one-pot thiol–ene reaction

2017 ◽  
Vol 41 (23) ◽  
pp. 14545-14550 ◽  
Author(s):  
Yujing Zuo ◽  
Zhiming Gou ◽  
Zhaoyue Li ◽  
Jinwan Qi ◽  
Shengyu Feng
Keyword(s):  
Ionic Liquid ◽  
Ionic Liquids ◽  
Self Assembly ◽  
High Yield ◽  
Imidazolium Ionic Liquid ◽  
One Pot ◽  
Ene Reaction ◽  
Imidazolium Ionic Liquids ◽  
Film Forming ◽  
Photoluminescence Behavior

The synthesis of a series of polysiloxane-based ionic liquids (PNLs) is reported via straightforward thiol–ene reaction with high yield using three kinds of imidazolium ionic liquid monomers.

One-Pot Synthesis of Ion-Containing CO2-Based Polycarbonates Using Protic Ionic Liquids as Chain Transfer Agents

2018 ◽  
Vol 51 (22) ◽  
pp. 9122-9130 ◽  
Author(s):  
Zhaohe Huang ◽  
Yanyan Wang ◽  
Na Zhang ◽  
Luhong Zhang ◽  
Donald J. Darensbourg
Keyword(s):  
Ionic Liquids ◽  
Chain Transfer ◽  
Protic Ionic Liquids ◽  
One Pot ◽  
One Pot Synthesis ◽  
Transfer Agents

One-Pot Synthesis of Silica Gel Confined Functional Ionic Liquids: Effective Catalysts for Deoximation under Mild Conditions.

ChemInform ◽  
2004 ◽  
Vol 35 (15) ◽  
Author(s):  
Dongmei Li ◽  
Feng Shi ◽  
Shu Guo ◽  
Youquan Deng
Keyword(s):  
Ionic Liquids ◽  
Silica Gel ◽  
One Pot ◽  
Mild Conditions ◽  
One Pot Synthesis

One-pot synthesis of cobalt-coordinated N-doped carbon catalysts via co-synthesis of ionic liquids and cobalt porphyrins

2015 ◽  
Vol 51 (93) ◽  
pp. 16637-16640 ◽  
Author(s):  
Yuan Chen ◽  
Lingling Fu ◽  
Zhigang Liu
Keyword(s):  
Ionic Liquids ◽  
One Pot ◽  
One Pot Synthesis ◽  
Cobalt Porphyrins ◽  
Carbon Catalysts

Cobalt-coordinated N-doped carbon (CoNC) was fabricated by heating cobalt porphyrins and ionic liquids.

Demulsification of water in crude oil emulsion using long chain imidazolium ionic liquids and optimization of parameters

Fuel ◽  
2018 ◽  
Vol 229 ◽  
pp. 126-134 ◽  
Author(s):  
Nastaran Hazrati ◽  
Ali Akbar Miran Beigi ◽  
Majid Abdouss
Keyword(s):  
Ionic Liquids ◽  
Crude Oil ◽  
Oil Emulsion ◽  
Optimization Of Parameters ◽  
Imidazolium Ionic Liquids ◽  
Long Chain

A new one-pot synthesis of μ-oxo dimeric iron(III) porphyrins from meso-tetraarylporphyrins

2009 ◽  
Vol 13 (08n09) ◽  
pp. 854-858 ◽  
Author(s):  
Qiang Liu ◽  
Yan-Zhi Gong ◽  
Chang-Jun Gong ◽  
Qing-Hong Li ◽  
Can-Cheng Guo
Keyword(s):  
Synthetic Methods ◽  
High Yield ◽  
Reaction Intermediates ◽  
Ferrous Chloride ◽  
Iron Porphyrins ◽  
One Pot ◽  
Convenient Procedure ◽  
One Pot Synthesis ◽  
New Synthesis ◽  
The One

A new synthesis of μ-oxo dimeric iron(III) porphyrins from meso-tetraarylporphyrins in one-pot procedure is reported. μ-oxo dimeric iron(III) porphyrin was obtained in high yield (up to 93%) from the reaction of meso-tetraarylporphyrin with ferrous chloride in DMF at pH 8–11. Compared with other synthetic methods of μ-oxo dimeric iron(III) porphyrin from meso-tetraarylporphyrins, the one-pot procedure has higher yields of μ-oxo dimeric iron(III) porphyrins and is a simpler and more convenient procedure. In order to evaluate the range of applicability of this method, μ-oxo dimeric iron(III) porphyrins with different substituents were prepared by the reaction of the corresponding meso-tetraarylporphyrins with ferrous chloride. The results showed that it was possible to apply this one-pot procedure to the synthesis of other μ-oxo dimeric iron porphyrins in excellent yields. A mechanism for the formation of μ-oxo dimeric iron porphyrins was proposed based on the reaction intermediates characterized by HPLC and UV-vis methods.

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