Superoxide protonation by weak acids in imidazolium based ionic liquids.
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Summary
The mechanism of the reduction of O2 in the presence of the different phenols was found to be very similar in [BMIm][TFSI] and in DMF: A 2-electron mechanism involving a succession of electrochemical and protonation steps.
- Type
- dissertation
- Published
- 2009-02-10
- Cited by
- 50
- References
- 0
- OpenAlex
- https://openalex.org/W19708214
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:11394770
Keywords
Service (business), Operations management, Business, Engineering management, Engineering
References
No references recorded for this paper.
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- Generation of superoxide ion in 1-butyl-1- methylpyrrolidinium trifluoroacetate and its application in the destruction of chloroethanes
- Carbon dioxide as carbon source: Activation via electrogenerated O2− in ionic liquids
- An investigation of the reaction between 1-butyl-3-methylimidazolium trifluoromethanesulfonate and superoxide ion
- Long term stability of superoxide ion in piperidinium, pyrrolidinium and phosphonium cations-based ionic liquids and its utilization in the destruction of chlorobenzenes
- Redox Chemistry of the Superoxide Ion in a Phosphonium-Based Ionic Liquid in the Presence of Water.
- Electrochemical oxygen reduction at soft interfaces catalyzed by the transfer of hydrated lithium cations
- A novel fabrication of a polymeric ionic liquid hybrid film modified electrode and its successful application to the electrogeneration of a superoxide anion in aqueous media.
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