scholarly journals Mutual Lewis Acid-Base Interactions of Cations and Anions in Ionic Liquids

2012 ◽  
Vol 19 (1) ◽  
pp. 288-293 ◽  
Author(s):  
Markus Holzweber ◽  
Ralf Lungwitz ◽  
Denise Doerfler ◽  
Stefan Spange ◽  
Mihkel Koel ◽  
...  
Keyword(s):  
2018 ◽  
Vol 20 (9) ◽  
pp. 2075-2083 ◽  
Author(s):  
Shaojuan Zeng ◽  
Lei Liu ◽  
Dawei Shang ◽  
Jianpeng Feng ◽  
Haifeng Dong ◽  
...  

Cobalt ionic liquids with highly efficient and reversible absorption of NH3 through Lewis acid–base and hydrogen bond interactions were designed.


2014 ◽  
Vol 50 (95) ◽  
pp. 15041-15044 ◽  
Author(s):  
Fang Ding ◽  
Xi He ◽  
Xiaoyan Luo ◽  
Wenjun Lin ◽  
Kaihong Chen ◽  
...  

Carbonyl-containing anion-functionalized ionic liquids exhibit a significant enhancement in CO2 capacity and excellent reversibility.


2020 ◽  
Vol 56 (40) ◽  
pp. 5362-5365 ◽  
Author(s):  
Rajkumar Kore ◽  
Steven P. Kelley ◽  
Anand D. Sawant ◽  
Manish Kumar Mishra ◽  
Robin D. Rogers

Unique Lewis acid/base liquid coordination catalysts were compared to the known super acidic ionic liquid chloroaluminates and found to have higher catalytic activity in the alkylation of benzene.


1980 ◽  
Vol 45 (2) ◽  
pp. 335-338 ◽  
Author(s):  
Adéla Kotočová ◽  
Ulrich Mayer

The solvation effect of a number of nonaqueous polar solvents was studied on the oxidation-reduction properties of the [Co(en)3]3+-[Co(en)3]2+ system. Interactions of these ions with the solvent molecules are discussed in terms of their coordination, which is accompanied by a specific interaction of the Lewis acid-base type, namely formation of a hydrogen bond between the interacting particles. This is the main controlling factor of the redox properties of the studied system.


2021 ◽  
Vol 60 (6) ◽  
pp. 3893-3901
Author(s):  
Douglas Turnbull ◽  
Praveen Chaudhary ◽  
Paul Hazendonk ◽  
Stacey D. Wetmore ◽  
Michael Gerken
Keyword(s):  

2021 ◽  
Vol 27 (1) ◽  
pp. 17-23
Author(s):  
Guniganti Balakishan ◽  
Gullapalli Kumaraswamy ◽  
Vykunthapu Narayanarao ◽  
Pagilla Shankaraiah

Abstract A Cu(II)-catalyzed Csp2-Se and Csp2-Sulfur bond formation was achieved with moderate to good yields without the aid of Lewis acid and base. The reaction is compatible with a wide range of heterocycles such as benzothiazole, thiazole, and imidazole. Also, this typical protocol is found to be active in thio-selenation via S-H activation. Additionally, we proposed a plausible mechanistic pathway involving Cu(III) putative intermediate.


Author(s):  
Shotaro Tada ◽  
Norifumi Asakuma ◽  
Shiori Ando ◽  
Toru Asaka ◽  
Yusuke Daiko ◽  
...  

This paper reports on the relationship between the H2 chemisorption properties and reversible structural reorientation of the possible active site around Al formed in-situ within polymer-derived ceramics (PDCs) based on...


Sign in / Sign up

Export Citation Format

Share Document