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dc.creatorYau, Josephen_US
dc.creatorKasha, Michaelen_US
dc.date.accessioned2006-06-15T13:39:36Z
dc.date.available2006-06-15T13:39:36Z
dc.date.issued1975en_US
dc.identifier1975-RH-02en_US
dc.identifier.urihttp://hdl.handle.net/1811/9387
dc.descriptionAuthor Institution: Department of Chemistry, Florida State Universityen_US
dc.description.abstractThe N-heterocyclic acridine exhibits two different fluorescences, depending on the nature of the solvent. In a hydroxylic solvent (EPA) glass, acridine exhibits a blue $\Pi$,$\Pi^{*}$ fluorescence, resembling that of the parent polyacene, anthracene. However, in a hydrocarbon glass, acridine shows a broad, structureless, green fluorescence. At $77^{\circ} K$, the lifetime of this emission is $2.5 \mu$sec in hydrocarbon glass. This emission is assigned as the n,$\Pi^{*}$ fluorescence. The lowest absorption spectra of acridine also show characteristic differences in the two kinds of solvents. The excitation spectrum of each fluorescence agrees with the corresponding absorption spectrum. Because of its long lifetime, the $\Pi$,$\Pi^{*}$ fluorescence is not observed readily in a fluid medium at room, temperature. In a low temperature glass, intersystem crossing competes favorably with the n,$\Pi^{*}$ fluorescence. Hence, the phosphorescence quantum yield of acridine is much higher in a hydrocarbon than in a hydroxylic solvent.en_US
dc.format.extent119251 bytes
dc.format.mimetypeimage/jpeg
dc.language.isoEnglishen_US
dc.publisherOhio State Universityen_US
dc.titlen,$\Pi^{*}$ AND $\Pi$,$\Pi^{*}$ FLUORESCENCES IN ACRIDINEen_US
dc.typearticleen_US


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