Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40825
Full metadata record
DC FieldValueLanguage
dc.contributor.authorSharma, Pratibha-
dc.contributor.authorDave, Archana-
dc.contributor.authorMishra, Nirankar N-
dc.contributor.authorNarad, Sandeep R-
dc.contributor.authorKapoor, Neeta-
dc.date.accessioned2017-03-20T06:39:33Z-
dc.date.available2017-03-20T06:39:33Z-
dc.date.issued1997-05-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40825-
dc.description449-452en_US
dc.description.abstractPresent note deals with the electrochemical behaviour of N-sulphonamoylphenyl-3-aminophenyl-5methyl- 4 -[4'(2"-pyrimidinyl)sulphonamoyl]-phenylazopyrazoles. All the studies have been carried out in DMF-water admixture using Britton-Robinson buffers of varying pH. A single, well defined, diffusion-controlled reduction wave is obtained which shifted towards more negative potential with increase in the pH. On the basis of number of protons consumed and electron transferred, a plausible mechanism has also 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.36A(05) [May 1997]en_US
dc.titleElectrochemical studies on somesynthesised N-sulphonamoylphenyl- 3-aminophenyl- 5-methyl-4-[ 4'(2"-pyrimidinyl)sulphonamoyl]- phenylazopyrazolesen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.36A(05) [May 1997]

Files in This Item:
File Description SizeFormat 
IJCA 36A(5) 449-452.pdf117.05 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.