Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/40212
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAmeerunisha, S-
dc.contributor.authorZacharias, P S-
dc.date.accessioned2017-02-07T11:30:25Z-
dc.date.available2017-02-07T11:30:25Z-
dc.date.issued1998-08-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/40212-
dc.description696-701en_US
dc.description.abstractThe absorption and emission spectra of the schiff base (I) derived from 2,6-diformyl-4-methylphenol and o-aminobenzoic acid have been investigated in various solvents like N,N- dimethylformamide, acetonitrile, methanol and chloroform. Only in N,N-dimethylformamide, formation of phenoxide and cleavage of the imine bond is observed accompanied by changes in absorption and emission spectra. Results on the metal complexes of schiff base (I) indicate that the generation of phenoxide and cleavage of -CH=N-bond are retarded by chelation with metal ions like Cd2+ or Z2+ without quenching the emission, whereas chelation with Cu2+ or Fe2+ ions results in complete quenching of emission.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.37A(08) [August 1998]en_US
dc.titleFluorescence emission in schiff bases of 2,6-diformyl-4-methylphenol: Effect of chelation on the emissionen_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.37A(08) [August 1998]

Files in This Item:
File Description SizeFormat 
IJCA 37A(8) 696-701.pdf546.11 kBAdobe PDFView/Open


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