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- W2048786075 abstract "Abstract Depending on the structure of the hydroxyiminoanthraquinone, the radical anion formed upon addition of one electron can either be stable in aprotic media, as already reported in the case of hydroxyanthraquinones, or protonated by the parent compound. Such a self-protonation induces the disproportionation of the semi-iminoquinone which becomes a shortlived species. The latter mechanism is studied in detail: it corresponds to a transition between the DISP1 and DISP2 regimes observed experimentally under mixed kinetic-diffusion control. The pertinent rate constants have been determined." @default.
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- W2048786075 date "1986-07-01" @default.
- W2048786075 modified "2023-10-01" @default.
- W2048786075 title "Mechanism of the eletrochemical reduction of hydroxyiminoanthraquinones in DMF" @default.
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- W2048786075 doi "https://doi.org/10.1016/0022-0728(86)87068-1" @default.
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