2010
DOI: 10.1016/j.jelechem.2010.07.016
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The electrochemical reduction of 1,4-benzoquinone in 1-ethyl-3-methylimidazolium bis(trifluoromethane-sulfonyl)-imide, [C2mim][NTf2]: A voltammetric study of the comproportionation between benzoquinone and the benzoquinone dianion

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Cited by 28 publications
(11 citation statements)
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“…For example, the electrochemical reduction of nitrobenzene and 4-nitrophenol in [C 4 dmim][NTf 2 ] [4], has been shown to follow the same generic mechanism in both ionic liquids and conventional solvents, such as dimethylformamide and dimethyl sulfoxide. Furthermore, the mechanism observed for the reduction of benzoquinone in [C 2 mim][NTf 2 ] is consistent with that reported in dimethyl formamide, propylene carbonate, and acetonitrile [5].…”
Section: Introductionsupporting
confidence: 86%
“…For example, the electrochemical reduction of nitrobenzene and 4-nitrophenol in [C 4 dmim][NTf 2 ] [4], has been shown to follow the same generic mechanism in both ionic liquids and conventional solvents, such as dimethylformamide and dimethyl sulfoxide. Furthermore, the mechanism observed for the reduction of benzoquinone in [C 2 mim][NTf 2 ] is consistent with that reported in dimethyl formamide, propylene carbonate, and acetonitrile [5].…”
Section: Introductionsupporting
confidence: 86%
“…The introduction of lithiumorganic hybrid flow battery systems can be traced back to the work of Senoh et al in 2011 [222] based on the two-electron reactions of 1,4-benzoquinone and its derivatives for lithium secondary batteries. The reaction mechanisms in non-aqueous media are similar to those of anthraquinone [181,182], as described in Section 4.1.7. and in the literature [224]:…”
Section: All-poly(boron-dipyrromethene) Redox Flow Battery (Asymmetric)mentioning
confidence: 97%
“…Extensive modeling of aw ide diversityo fv oltammetric systems has been undertaken using small microelectrodes in order to provide ab etter possibility of extracting kinetic parameters. Systems studied include O 2 /O 2 C À , [45] Br À /Br 2 , [48] nitrobenzenes, [49] aryl amines, [50] NO 2 /NO 2 À /NO 2 + , [51] I À /I 2, [52] aromatic diamines, [53] arenes, [54] Li/Li + , [55] benzoquinone, [56] hydroquinone, [57] and H + /H 2 . [58] In many cases the values of k 0 obtained correspond to quasi-reversible behaviour and, as such, do not provide ap erfect test of the validity of Butler-Volmer kinetics since the behaviour is approximately Nernstian.…”
Section: Voltammetry In Ionic Liquidsmentioning
confidence: 99%