Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/46813
Full metadata record
DC FieldValueLanguage
dc.contributor.authorBasu, Sekhar-
dc.contributor.authorPaul, Tapan K-
dc.contributor.authorRoy, Sarmila-
dc.date.accessioned2019-03-26T11:15:03Z-
dc.date.available2019-03-26T11:15:03Z-
dc.date.issued1989-09-
dc.identifier.issn0975-0975(Online); 0376-4710(Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/46813-
dc.description729-734en_US
dc.description.abstractEffects of Triton X-100 micelles on the absorption and emission properties of tetrakis(sulphonatophenyl)porphyrin (TPPS) have been studied. An analysis of the absorption spectra in terms of four-orbital model of porphyrin excited state reveals that there is no ground state complex formation. The TPPS molecule is strongly hydrophilic so there is very little possibility of its solubilization within neutral Triton X-100 micelles. Enhancement of fluorescence intensity with increase in surfactant concentration is caused by the surface adsorption of the TPPS molecule at the hydrophilic mantle of the micelle, i.e. the Stern layer, where it is exposed to water, and van der Waals interaction is the main binding force. The inhibition of the radiation less decay by micellar aggregates, rationalized in terms of rigidization of the TPPS by the local environment of the micelle, is further confirmed from fluorescence polarization spectroscopy.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.28A(09) [September 1989]en_US
dc.titleAbsorption and fluorescence spectra of tetrakis(sulphonatophenyl) porphyrin in Triton X-100 micelles: Analysis in terms of four-orbital model parameteren_US
dc.typeArticleen_US
Appears in Collections:IJC-A Vol.28A(09) [September 1989]

Files in This Item:
File Description SizeFormat 
IJCA 28A(9) 729-734.pdf3.63 MBAdobe PDFView/Open


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