The electrochemical behavior of nitrofurazone in dimethylformamide has been studied by cyclic voltammetry and in-situ thin-layer spectroelectrochemistry.The redox reactions are complicated at platinium electrode,and a...The electrochemical behavior of nitrofurazone in dimethylformamide has been studied by cyclic voltammetry and in-situ thin-layer spectroelectrochemistry.The redox reactions are complicated at platinium electrode,and a possible electrochemical mechanism of nitrofurazone is proposed.展开更多
The electrooxidation behavior of 3, 3′,5, 5′-tetramethylbenzidine(TMB) was investigated using a platinum minigrid optically transparent thin-layer spectroelectrochemical cell. TMB underwent one two-electron electroo...The electrooxidation behavior of 3, 3′,5, 5′-tetramethylbenzidine(TMB) was investigated using a platinum minigrid optically transparent thin-layer spectroelectrochemical cell. TMB underwent one two-electron electrooxidation process to yield quinonediimine in the pH range from 2.0 to < 4.0, and two consecutive one-electron electrooxidation processes, gave the mediate product free radical of TMB first, then gave the oxidation product quinonediimine in the pH range from 4.0 to < 7.0. In the pH range from 7.0 to 10.0, the electrooxidation of TMB was also one two-electron electrooxidation process to yield an azo compound. The formal potential E0'and the electron transfer number of the electrooxidation of TMB at pH 2.0 and pH 8.4 were determined by spectroelectrochemical techniques.展开更多
文摘The electrochemical behavior of nitrofurazone in dimethylformamide has been studied by cyclic voltammetry and in-situ thin-layer spectroelectrochemistry.The redox reactions are complicated at platinium electrode,and a possible electrochemical mechanism of nitrofurazone is proposed.
基金The project was supported by the National Natural Science Foundation of China(Grant No.20075013).
文摘The electrooxidation behavior of 3, 3′,5, 5′-tetramethylbenzidine(TMB) was investigated using a platinum minigrid optically transparent thin-layer spectroelectrochemical cell. TMB underwent one two-electron electrooxidation process to yield quinonediimine in the pH range from 2.0 to < 4.0, and two consecutive one-electron electrooxidation processes, gave the mediate product free radical of TMB first, then gave the oxidation product quinonediimine in the pH range from 4.0 to < 7.0. In the pH range from 7.0 to 10.0, the electrooxidation of TMB was also one two-electron electrooxidation process to yield an azo compound. The formal potential E0'and the electron transfer number of the electrooxidation of TMB at pH 2.0 and pH 8.4 were determined by spectroelectrochemical techniques.
