Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/22740
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPujari, S R-
dc.contributor.authorBhosale, P N-
dc.contributor.authorRao, P M R-
dc.contributor.authorPatil, S R-
dc.date.accessioned2013-10-28T09:53:52Z-
dc.date.available2013-10-28T09:53:52Z-
dc.date.issued2003-05-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/22740-
dc.description251-256en_US
dc.description.abstractPhotophysical properties of bifunctional N-phenylanthranilic acid (NPAA) have been studied as a dopant in polystyrene (PS) films. The PS films containing fluorescent NPAA were prepared from the solutions in non-polar and polar solvents. The fluorescence spectra of PS films prepared by using non-polar solvents depend on the concentration of NPAA in the film. The films containing lower concentration have exhibited sharp emission band at 412 nm corresponding to normal emission while the films containing higher concentration of NPAA have shown broad emission band peaking at 466 nm. The broad emission band is attributed to as arising due to formation of dimeric species by hydrogen bonding between two neighbouring NPAA molecules in the films. The modification observed in the fluorescence excitation and absorption spectra of the films with dopant concentration allows to consider the interaction between dopant molecules. In case of NPAA doped poly(vinyl acetate) films, there is an evidence for the destabilization of dimeric species as the fluorescence corresponds to the normal emission only.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.sourceIJCT Vol.10(3) [May 2003]en_US
dc.titlePhotophysical studies of N-phenylanthranilic acid in polymer filmsen_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.10(3) [May 2003]

Files in This Item:
File Description SizeFormat 
IJCT 10(3) 251-256.pdf1.26 MBAdobe PDFView/Open


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