Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/14630
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dc.contributor.authorJain, Rajeev-
dc.contributor.authorKaraiya, Shrinarayan-
dc.contributor.authorYadav, Ramji Lal-
dc.contributor.authorArya, Virendra K-
dc.date.accessioned2012-08-31T09:33:07Z-
dc.date.available2012-08-31T09:33:07Z-
dc.date.issued2012-09-
dc.identifier.issn0975-1084 (Online); 0022-4456 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/14630-
dc.description606-611en_US
dc.description.abstractThis study presents synthesis of 3-[4'-(substituted) sulphonamoylphenyl] azomethine indoles (SPAI) by refluxing indole-3-carboxaldehyde with sulfonamide derivatives. Electrochemical behaviour of SPAI was studied in Britton-Robinson (BR) buffer solution (pH 2.5-12.0) at dropping mercury electrode (DME) and glassy carbon electrode (GCE). Cathodic differential pulse polarographic peak was obtained at DME in pH range 2.5-6.5. Cyclic voltammogram exhibited a well defined, irreversible cathodic and anodic peak at GCE. At pH 6.5 and above, reduction peak exhibited a tendency to split into two peaks, indicating that 1H+/2e- reduction of 2-[4’-sulphonamoylphenyl]hydrazono-1,3-indanediones occurs in one 1H+ and one 2e- steps. A product of CPE was characterized by elemental and spectral analyses.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.sourceJSIR Vol.71(09) [September 2012]en_US
dc.subjectControlled potential electrolysis (CPE)en_US
dc.subjectCyclic voltammetryen_US
dc.subjectDifferential pulse polarographyen_US
dc.subject3-[4'-(substituted) Sulphonamoylphenyl] azomethine indoles (SPAI)en_US
dc.titleSynthesis and electrochemical behaviour of 3-[4'-(substituted) sulphonamoylphenyl] azomethine indolesen_US
dc.typeArticleen_US
Appears in Collections:JSIR Vol.71(09) [September 2012]

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