Goux Aurélie, Pratt Dominic, Dunsch Lothar
Abteilung Elektrochemie und leitfähige Polymere, Leibniz-Institut für Festkörper- und Werkstoffforschung Dresden, Helmholtzstrasse 20, 01069 Dresden, Germany.
Chemphyschem. 2007 Oct 8;8(14):2101-6. doi: 10.1002/cphc.200700235.
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.
采用原位电子自旋共振-紫外/可见光谱电化学方法,以深入了解对甲苯二胺在不同pH值的水溶液中进行阳极氧化时的中间体和反应产物。发现阳离子自由基的稳定性强烈依赖于pH值。虽然在pH为2和10时通过电子自旋共振光谱证明不存在稳定自由基,但在中等pH值下检测到该自由基,并将其归属于半醌二亚胺结构。在这些pH值下也观察到了该自由基的紫外/可见吸收。在所有pH值下,通过紫外/可见光谱跟踪电极反应过程中的对甲苯二亚胺中间体和三聚反应产物。