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dc.contributor.authorSaji Alex-
dc.contributor.authorBasheer, M C-
dc.contributor.authorArun, K T-
dc.contributor.authorRamaiah, D-
dc.contributor.authorSuresh Das-
dc.date.accessioned2014-10-18T06:36:44Z-
dc.date.available2014-10-18T06:36:44Z-
dc.date.issued2007-
dc.identifier.citationJournal of Physical Chemistry A 111(17):3226-3230;3 May 2007en_US
dc.identifier.issn1089-5639-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1685-
dc.description.abstractThe squaraine dye bis(2,4,6-trihydroxyphenyl)squaraine (SqH) was earlier reported to form J-type dimer aggregates in acetonitrile solutions at higher concentrations. Subsequent studies have suggested that concentration-dependent changes in the absorption spectrum of SqH in acetonitrile could be attributed to shifts in the acid-base equilibrium due to the presence of water as an impurity. In this work, we describe our studies on the effect of varying acid and dye concentration on the absorption spectra of the bromo and iodo substituted dyes, bis(3,5-dibromo-2,4,6-trihydroxyphenyl)squaraine (SqBr) and bis(3,5-diiodo-2,4,6-trihydroxyphenyl)squaraine (SqI). Analysis of the changes in the absorption spectra as a function of dye concentration and the nature of the solvent composition confirmed the formation of J-type dimer aggregates in aprotic solvents in this class of dyes. Further confirmation for the formation of the J-type dimer aggregates could be obtained by comparing the differences in the triplet excited state properties of the neutral and aggregated forms of the dyes using time-resolved spectroscopy.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectLangmuir-blodgett-filmsen_US
dc.subjectExcited-state propertiesen_US
dc.subjectPhotodynamic therapyen_US
dc.subjectAqueous-mediaen_US
dc.subjectBis(2,4,6-trihydroxyphenyl)squaraineen_US
dc.subjectPhotochemistryen_US
dc.subjectDNAen_US
dc.subjectCytotoxicityen_US
dc.subjectPhotophysicsen_US
dc.titleAggregation properties of heavy atom substituted squaraine dyes: Evidence for the formation of J-type dimer aggregates in aprotic solventsen_US
dc.typeArticleen_US
niist.citation-
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