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- W2020113269 endingPage "771" @default.
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- W2020113269 abstract "The kinetics of nucleophilic aromatic substitution of three nitrothiophene derivatives in different [1-butyl-3-methylimidazolium][N3]/ionic liquid binary mixtures was studied spectrophotometrically at 298 K. Ionic liquids differing for cation structure (imidazolium or pyrrolidinium) and for size, shape, and coordination ability of the anion ([BF4−], [PF6−], [SbF6−], and [NTf2−]) were used. Furthermore, in order to have a comparison with conventional organic solvents, the target reaction was also carried out in DMF solution at increasing concentration of NaN3 or [bmim][N3]. Data collected show that the reaction occurs faster in DMF than in ionic liquid solution. Furthermore, as a consequence of the ability of all solvent media to favor the leaving group departure, a simple linear dependence of the pseudo-first-order kinetic constant from nucleophile concentration was detected. The results of this kinetic investigation once more underline that ionic liquids are able to exert peculiar effects that can be understood also considering their three-dimensional organization." @default.
- W2020113269 created "2016-06-24" @default.
- W2020113269 creator A5047757372 @default.
- W2020113269 creator A5070055086 @default.
- W2020113269 creator A5087159187 @default.
- W2020113269 date "2009-12-29" @default.
- W2020113269 modified "2023-09-23" @default.
- W2020113269 title "Aryl Azides Formation Under Mild Conditions: A Kinetic Study in Some Ionic Liquid Solutions" @default.
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- W2020113269 doi "https://doi.org/10.1021/jo9022952" @default.
- W2020113269 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/20039644" @default.
- W2020113269 hasPublicationYear "2009" @default.
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