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The reaction mechanism of p-toluenediamine anodic oxidation: an in situ ESR-UV/Vis/NIR spectroelectrochemical study.
Authors:Aurélie Goux  Dominic Pratt  Lothar Dunsch
Affiliation:1. Abteilung Elektrochemie und leitf?hige Polymere, Leibniz‐Institut für Festk?rper‐ und Werkstoffforschung Dresden, Helmholtzstra?e 20, 01069 Dresden, Germany, Fax: (+49)?351‐4659‐811;2. Kao Corporation, KPSS, R&D Centre, Pfungstadter Stra?e 100, 64297 Darmstadt, Germany
Abstract:In situ ESR-UV/Vis spectroelectrochemistry is applied to obtain new insights into the intermediates and reaction products of the anodic oxidation of p-toluenediamine in aqueous solution at different pH values. A strong pH dependence of the stability of the cation radical is found. While the absence of a stable radical was proved by ESR spectroscopy at pH 2 and 10, this radical is detected at medium pH values and assigned to the semiquinonediimine structure. The UV/Vis absorption of the radical is observed at these pH values as well. The p-toluenediimine intermediate and the trimeric reaction product were followed during the electrode reaction by UV/Vis spectroscopy at all pH values.
Keywords:electrochemistry  EPR spectroscopy  oxidation  toluenediamine  UV/Vis spectroscopy
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