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Study of the reduction mechanism of the N-oxides of pyridine monocarboxylic acids at mercury electrodes

✍ Scribed by M.A. Zón; M. Angulo; J.M. Rodríguez Melladore

Publisher
Elsevier
Year
1994
Tongue
English
Weight
714 KB
Volume
365
Category
Article
ISSN
1572-6657

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The polarographic reduction of erythrosin, the disodium salt of 2',4',5',7'-tetraiodofluorescein, was examined at pH 4.7. Three reduction steps were found. The first step involves two electrons and the reduction of the quinone group as in fluorescein. The second step results from the removal of the