scholarly journals A structural investigation of ionic liquid mixtures

2016 ◽  
Vol 18 (12) ◽  
pp. 8608-8624 ◽  
Author(s):  
Richard P. Matthews ◽  
Ignacio J. Villar-Garcia ◽  
Cameron C. Weber ◽  
Jeraime Griffith ◽  
Fiona Cameron ◽  
...  

The role of hydrogen bonding, π+–π+ stacking and anion–π+ interactions on the structure of ionic liquid mixtures has been elucidated through a combined theoretical and experimental approach.

2016 ◽  
Vol 18 (48) ◽  
pp. 32723-32734 ◽  
Author(s):  
Kaixin Li ◽  
Yibo Yan ◽  
Jun Zhao ◽  
Junxi Lei ◽  
Xinli Jia ◽  
...  

The intra- and inter-hydrogen bonding networks that govern the catalytic activity of Brønsted acidic ionic liquids were identified.


AIChE Journal ◽  
2012 ◽  
Vol 59 (5) ◽  
pp. 1657-1667 ◽  
Author(s):  
Qiwei Yang ◽  
Huabin Xing ◽  
Baogen Su ◽  
Zongbi Bao ◽  
Jun Wang ◽  
...  

2012 ◽  
Vol 116 (4) ◽  
pp. 1360-1369 ◽  
Author(s):  
Shruti Trivedi ◽  
Shubha Pandey ◽  
Sheila N. Baker ◽  
Gary A. Baker ◽  
Siddharth Pandey

Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 721 ◽  
Author(s):  
Young-Ho Oh ◽  
Hyoju Choi ◽  
Chanho Park ◽  
Dong Wook Kim ◽  
Sungyul Lee

We review recent works for nucleophilic fluorination of organic compounds in which the Coulombic interactions between ionic species and/or hydrogen bonding affect the outcome of the reaction. SN2 fluorination of aliphatic compounds promoted by ionic liquids is first discussed, focusing on the mechanistic features for reaction using alkali metal fluorides. The influence of the interplay of ionic liquid cation, anion, nucleophile and counter-cation is treated in detail. The role of ionic liquid as bifunctional (both electrophilic and nucleophilic) activator is envisaged. We also review the SNAr fluorination of diaryliodonium salts from the same perspective. Nucleophilic fluorination of guanidine-containing of diaryliodonium salts, which are capable of forming hydrogen bonds with the nucleophile, is exemplified as an excellent case where ionic interactions and hydrogen bonding significantly affect the efficiency of reaction. The origin of experimental observation for the strong dependence of fluorination yields on the positions of -Boc protection is understood in terms of the location of the nucleophile with respect to the reaction center, being either close to far from it. Recent advances in the synthesis of [18F]F-dopa are also cited in relation to SNAr fluorination of diaryliodonium salts. Discussions are made with a focus on tailor-making promoters and solvent engineering based on ionic interactions and hydrogen bonding.


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