Open Access
Open access
volume 27 issue 17 pages 5702

Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives

Publication typeJournal Article
Publication date2022-09-04
scimago Q1
wos Q2
SJR0.865
CiteScore8.6
Impact factor4.6
ISSN14203049
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Abstract

Besides their extremely useful properties as solvent, ionic liquids (ILs) are now considered to be highly instructive tools for enhancing the rates of chemical reactions. The ionic nature of the IL anion and cation seems to be the origin of this fascinating function of ILs as organocatalyst/promoter through their strong Coulombic forces on other ionic species in the reaction and also through the formation of hydrogen bonds with various functional groups in substrates. It is now possible to tailor-make ILs for specific purposes as solvent/promoters in a variety of situations by carefully monitoring these interactions. Despite the enormous potentiality, it seems that the application of ILs as organocatalysts/promoters for chemical reactions have not been fully achieved so far. Herein, we review recent developments of ILs for promoting the nucleophilic reactions, focusing on fluorination. Various aspects of the processes, such as organocatalytic capability, reaction mechanisms and salt effects, are discussed.

Found 
Found 

Top-30

Journals

1
Catalysts
1 publication, 7.69%
Journal of Fluorine Chemistry
1 publication, 7.69%
Molecules
1 publication, 7.69%
Russian Chemical Reviews
1 publication, 7.69%
Acta Chimica Sinica
1 publication, 7.69%
Catalysis Letters
1 publication, 7.69%
Reaction Chemistry and Engineering
1 publication, 7.69%
RSC Advances
1 publication, 7.69%
Journal of Molecular Structure
1 publication, 7.69%
Bulletin of the Korean Chemical Society
1 publication, 7.69%
Nature Communications
1 publication, 7.69%
ChemistrySelect
1 publication, 7.69%
Circular Economy in Engineering Design and Production
1 publication, 7.69%
1

Publishers

1
2
3
Springer Nature
3 publications, 23.08%
MDPI
2 publications, 15.38%
Elsevier
2 publications, 15.38%
Royal Society of Chemistry (RSC)
2 publications, 15.38%
Wiley
2 publications, 15.38%
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
1 publication, 7.69%
Shanghai Institute of Organic Chemistry
1 publication, 7.69%
1
2
3
  • We do not take into account publications without a DOI.
  • Statistics recalculated weekly.

Are you a researcher?

Create a profile to get free access to personal recommendations for colleagues and new articles.
Metrics
13
Share
Cite this
GOST |
Cite this
GOST Copy
Oh Y., Kim D. W., Lee S. Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives // Molecules. 2022. Vol. 27. No. 17. p. 5702.
GOST all authors (up to 50) Copy
Oh Y., Kim D. W., Lee S. Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives // Molecules. 2022. Vol. 27. No. 17. p. 5702.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.3390/molecules27175702
UR - https://doi.org/10.3390/molecules27175702
TI - Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives
T2 - Molecules
AU - Oh, Young-Ho
AU - Kim, Dong Wook
AU - Lee, Sungyul
PY - 2022
DA - 2022/09/04
PB - MDPI
SP - 5702
IS - 17
VL - 27
PMID - 36080470
SN - 1420-3049
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2022_Oh,
author = {Young-Ho Oh and Dong Wook Kim and Sungyul Lee},
title = {Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives},
journal = {Molecules},
year = {2022},
volume = {27},
publisher = {MDPI},
month = {sep},
url = {https://doi.org/10.3390/molecules27175702},
number = {17},
pages = {5702},
doi = {10.3390/molecules27175702}
}
MLA
Cite this
MLA Copy
Oh, Young-Ho, et al. “Ionic Liquids as Organocatalysts for Nucleophilic Fluorination: Concepts and Perspectives.” Molecules, vol. 27, no. 17, Sep. 2022, p. 5702. https://doi.org/10.3390/molecules27175702.