Electrochemical studies of CO2in imidazolium ionic liquids using silver as a working electrode: a suitable approach for determining diffusion coefficients, solubility values, and electrocatalytic effects

RSC Advances ◽  
2014 ◽  
Vol 4 (110) ◽  
pp. 65176-65183 ◽  
Author(s):  
Irene Reche ◽  
Iluminada Gallardo ◽  
Gonzalo Guirado
2011 ◽  
Vol 56 (9) ◽  
pp. 3209-3218 ◽  
Author(s):  
Tzi-Yi Wu ◽  
Shyh-Gang Su ◽  
H. Paul Wang ◽  
Yuan-Chung Lin ◽  
Shr-Tusen Gung ◽  
...  

2019 ◽  
Vol 21 (5) ◽  
pp. 2567-2571 ◽  
Author(s):  
Marcileia Zanatta ◽  
Víctor U. Antunes ◽  
Cláudio F. Tormena ◽  
Jairton Dupont ◽  
Francisco P. dos Santos

Diffusion-ordered spectroscopy (DOSY) is a powerful method for the NMR analysis of ionic liquids. Thus the dynamic-structural behaviour of imidazolium ionic liquids has been investigated by measurements of direct 1H diffusion coefficients in different solvents.


2021 ◽  
Vol 105 ◽  
pp. 103210
Author(s):  
Mariusz Zalewski ◽  
Tomasz Krawczyk ◽  
Agnieszka Siewniak ◽  
Aleksander Sobolewski

2021 ◽  
Vol 412 ◽  
pp. 128624
Author(s):  
Tian-Lin Ren ◽  
Xi-Wen Ma ◽  
Xiao-Qiong Wu ◽  
Li Yuan ◽  
Yang-Li Lai ◽  
...  

2021 ◽  
Vol 341 ◽  
pp. 130029
Author(s):  
Wenyan Yin ◽  
Khaled Tawfik Alali ◽  
Milin Zhang ◽  
Jingyuan Liu ◽  
Dalei Song ◽  
...  

Author(s):  
Justyna Łuczak ◽  
Jan Hupka ◽  
Jorg Thöming ◽  
Christian Jungnickel

2015 ◽  
Vol 11 ◽  
pp. 1641-1648 ◽  
Author(s):  
A Srinivas Reddy ◽  
Kenneth K Laali

Reaction of benzyl and ethyl allenoates with TMSX (X = I, Br, Cl) and with NH4SCN were investigated in MeCN, DMF, and in imidazolium ionic liquids [BMIM][NTf2] and [BMIM][PF6] as solvent, in the presence and absence of Selectfluor. Comparative product analysis studies demonstrate that the ability of Selectflour to promote oxidative/electrophilic dihalogenation/dithiocyanation with TMSX/NH4SCN (as observed previously for 1-arylallenes) is diminished in allenoates, most significantly in reactions with TMSCl, and essentially disappearing in reactions with NH4SCN, in favor of nucleophilic/conjugate addition. The study underscores the contrasting reactivity patterns in 1-arylallenes and allenoates toward electrophilic and nucleophilic additions in halofunctionalization with TMSX/Selectfluor and thiocyanation reactions with NH4SCN/Selectfluor. These competing pathways are influenced by the nature of the anion, allene structure, and the choice of solvent.


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