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- W2081617963 abstract "The electŕochemical reduction of phenazine, P, in tetrahydrofuran is examined when no proton donor is added. The anion radical obtained after the first electron uptake is stable. The dianion is slowly protonated by residual water to PH−, which is deprotonated, upon reoxidation , by the OH− ions. Upon addition of proton donors of increasing strength, protonation of the species P−2, P.−, PH− and P is observed. The neutral radical PH. gives very rapidly, via an antidisproportionation, P and PH2. The different reduction mechanisms are discussed." @default.
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- W2081617963 date "1991-01-01" @default.
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- W2081617963 title "Reduction mechanism of phenazine in tetrahydrofuran. Influence of added proton donors" @default.
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- W2081617963 doi "https://doi.org/10.1016/0013-4686(91)85277-e" @default.
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