In situ spectroelectrochemistry of 2,5-diphenyl-1,3,4-oxadiazole

被引:17
|
作者
Kress, L [1 ]
Neudeck, A [1 ]
Petr, A [1 ]
Dunsch, L [1 ]
机构
[1] IFW DRESDEN EV,INST FESTKORPERFORSCH,ABT ELEKTROCHEM & LEITFAHIGE POLYMERE,D-01069 DRESDEN,GERMANY
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1996年 / 414卷 / 01期
关键词
2,5-diphenyl-1,3,4-oxadiazole; reduction mechanism; cyclic voltammetry; spectroelectrochemistry;
D O I
10.1016/0022-0728(96)04645-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The electrochemical reduction of 2,5-diphenyl-1,3,4-oxadiazole has been studied by both cyclic voltammetry and spectroelectrochemistry. The in situ spectroscopic techniques were applied to obtain structural information on the products of the follow-up reactions. Time-resolved UV-vis spectroscopy, with spectra measured on a time scale of 20 ms by a diode array spectrometer, was used in cyclic voltammetry to obtain up to 60 single spectra in the forward and backward scans. The radical anion of 2,5-diphenyl-1,3,4-oxadiazole, which is formed in the electron transfer reaction at the electrode, was studied by ESR spectroscopy. Furthermore, paramagnetic products of the follow-up reactions were detected. A reaction mechanism is formulated that includes an irreversible protonation reaction and, in parallel, a reversible ion-pairing reaction with the supporting electrolyte cation for the electrochemically generated radical anion and an irreversible follow-up reaction for the dianion of 2,5-diphenyl-1,3,4-oxadiazole.
引用
收藏
页码:31 / 40
页数:10
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