Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/19163
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dc.contributor.authorBASHEIR A. EL-SHETARY-
dc.contributor.authorMOHAMED S-
dc.contributor.authorABDEL-MOEZ-
dc.contributor.authorFAROUK I. ZIDAN-
dc.contributor.authorSHAKER L. STEVAN-
dc.date.accessioned2023-03-14T06:33:23Z-
dc.date.available2023-03-14T06:33:23Z-
dc.date.issued1988-09-20-
dc.identifier.citationBASHEIR, A., MOHAMED, S. A. M., FAROUK, I. Z., & SHAKER, L. S. (1988). Department of Chemistry, Faculty of Education Ain Shams University, Cairo HeZ1'. 0p0Z1'. s. J. Chem. Soc. Pak, 10(2).en_US
dc.identifier.issn0253-5106-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/19163-
dc.description.abstractPolarographic studies of some sulphonic aryl (or napthol ) hydrazono -I-phenyl -3-methyl -2-pyraz01in-5-one have been carried out in ethyl alcohol B. R. buffer solutions in the pH range 1.8 - 12.0. The nurrber of reduction waves was found to depend on the pH value of the solution and the structure of the dye stuff. All the conpounds gave a single, well defined irreversible wave between values 2.0-9.0. The E Of this wave is pH dependent but its i remains almst constant throughout the entire range. The E was shifted towards more negative potential showing that protonation preceeds reduction. The sulphonic group causes a shift of the wave and plateau suffers a minimum at value higher than 9.0. The reduction corresponds to consumption of four electrons leading to the amine stage. A general npchanism for the reduction process is suggested and discussed.en_US
dc.language.isoenen_US
dc.publisherHEJ Research Institute of Chemistry, University of Karachi, Karachi.en_US
dc.titlePolarographic Behaviour of Some Sulphonic—aryl—hydrazono Dyes Pyrazolin-5-one Dyesen_US
dc.typeArticleen_US
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