Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46258
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dc.contributor.authorVenkataramana, P-
dc.contributor.authorSuryanarayana, B Sathya-
dc.contributor.authorRavindranath, L K-
dc.contributor.authorSeshagiri, V-
dc.contributor.authorRao, S Brahmaji-
dc.date.accessioned2019-03-20T07:13:43Z-
dc.date.available2019-03-20T07:13:43Z-
dc.date.issued1990-01-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46258-
dc.description53-55en_US
dc.description.abstractElectrochemical reduction of 1-anilinomalonyl-3- methyl-4-(substituted benzeneazo )-5-pyrazolones (Ia-d) has been carried out in Britton-Robinson buffers in the pH range of 2-10. All the compounds give single, well-defined, diffusion-controlled, irreversible reduction wave at d.m.e. and well-defined cathodic peak at hanging drop mercury electrode. Based on the results obtained from polarography, cyclic voltammetry and microcoulornetry, a plausible mechanism has been suggested.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-A Vol.29A(01) [January 1990]en_US
dc.titleElectrochemical behaviour of 1-anilinomalonyl- 3-methyl-4-(substituted benzeneazo)-5-Pyrazolonesen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.29A(01) [January 1990]

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