2005
DOI: 10.1016/j.jelechem.2005.06.013
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Heterogeneous electron-transfer kinetics of nitro compounds in room-temperature ionic liquids

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Cited by 89 publications
(103 citation statements)
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References 51 publications
(93 reference statements)
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“…It has been reported that the long-term diffusive response in the dielectric spectrum reflect ion reorientation [26]. A marked decrease in the electron transfer rate constant was observed in the reduction of nitro-aromatic compounds in ionic liquids [52]. This change was attributed to the increase in the inner-sphere reorganization energy because of ion-pairing processes.…”
Section: Half-wave Potentials and Heterogeneous Electron Transfer Kinmentioning
confidence: 97%
“…It has been reported that the long-term diffusive response in the dielectric spectrum reflect ion reorientation [26]. A marked decrease in the electron transfer rate constant was observed in the reduction of nitro-aromatic compounds in ionic liquids [52]. This change was attributed to the increase in the inner-sphere reorganization energy because of ion-pairing processes.…”
Section: Half-wave Potentials and Heterogeneous Electron Transfer Kinmentioning
confidence: 97%
“…1 In general, the amino aryl compounds can be obtained by the reduction of the nitro aryl compounds. There are several approaches to realize the reduction process: metal/acid reduction, 2,3 catalytic hydrogenation, 4-6 electrolytic reduction, 7 homogeneous catalytic transfer hydrogenation, 8 heterogeneous catalytic transfer hydrogenation, 9-13 etc. However, these methods have certain shortcomings:…”
Section: Introductionmentioning
confidence: 99%
“…[9][10][11][12][13][14][15][16][17][18][19][20][21][22] Reports on more fundamental investigations such as the rate of heterogeneous electron transfer in this media have been less common. Hapiot and co-workers recently reported the heterogeneous rate constants for the reduction of a series of nitroaromatic and aliphatic compounds in 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)A C H T U N G T R E N N U N G imide and triethylbutylammonium bis(trifluoromethylsulfonyl)-imide [23] as well as for the oxidation of ferrocene in 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide. [16] Doherty and co-workers also measured the heterogeneous rate constants for the reduction of benzaldehyde in two different ionic liquids.…”
mentioning
confidence: 99%