Experimental and theoretical studies on hydrogen bond-promoted fixation of carbon dioxide and epoxides in cyclic carbonates

2012 ◽  
Vol 14 (31) ◽  
pp. 11021 ◽  
Author(s):  
Jin-Quan Wang ◽  
Jian Sun ◽  
Wei-Guo Cheng ◽  
Kun Dong ◽  
Xiang-Ping Zhang ◽  
...  
2019 ◽  
Vol 43 (7-8) ◽  
pp. 248-256
Author(s):  
Quan-Yao Liu ◽  
Lei Shi ◽  
Ning Liu

Hydroxyl- and carboxyl-functionalized imidazolium halides are used as efficient bifunctional organocatalysts for the synthesis of cyclic carbonates from CO2 and epoxides under mild reaction conditions. Control experiments suggest that the cycloaddition reaction is realized by the combination of the nucleophilic halide anions with hydroxyl and carboxyl groups as hydrogen bond donors. Moreover, the bifunctional organocatalysts can be easily recycled five times by simple filtration; however, a loss of activity was observed.


2015 ◽  
Vol 17 (8) ◽  
pp. 5959-5965 ◽  
Author(s):  
Mengshuai Liu ◽  
Kunqi Gao ◽  
Lin Liang ◽  
Fangxiao Wang ◽  
Lei Shi ◽  
...  

Experimental and DFT studies demonstrated that additional EG could cooperate with ILs to facilitate the cycloaddition reactionviahydrogen bond activation.


2018 ◽  
Vol 6 (4) ◽  
pp. 5322-5332 ◽  
Author(s):  
Felipe de la Cruz-Martínez ◽  
Javier Martínez ◽  
Miguel A. Gaona ◽  
Juan Fernández-Baeza ◽  
Luis F. Sánchez-Barba ◽  
...  

Synlett ◽  
2017 ◽  
Vol 28 (18) ◽  
pp. 2439-2444 ◽  
Author(s):  
Frank Jensen ◽  
Troels Skrydstrup ◽  
Mathias Flinker ◽  
Sara Lopez ◽  
Dennis Nielsen ◽  
...  

Three disilanes, (CH3)3SiSi(CH3)3, Cl(CH3)2SiSi(CH3)2Cl, and Cl2(CH3)SiSi(CH3)Cl2, all representing components of the Direct Process residue for the industrial synthesis of chloromethylsilanes, were evaluated for their abilities to reduce carbon dioxide to carbon monoxide upon treatment with fluoride salts. In particular, Cl(CH3)2SiSi(CH3)2Cl proved to be highly efficient upon the use of stoichiometric amounts of potassium bifluoride. DFT calculations performed on the reduction steps with (CH3)3SiSi(CH3)3 and fluorinated analogues of this disilane suggest that the previously proposed pathway involving an intermediate silacarboxylic acid is plausible.


1982 ◽  
Vol 87 (B12) ◽  
pp. 10215 ◽  
Author(s):  
Fraser P. Fanale ◽  
W. Bruce Banerdt ◽  
R. Steven Saunders ◽  
L. A. Johansen ◽  
James R. Salvail

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