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LIFETIME BROADENING IN THE ROTATIONALLY RESOLVED ELECTRONIC SPECTRA OF SOME FURAN DERIVATIVES AND ANALOGS IN THE GAS PHASE

Please use this identifier to cite or link to this item: http://hdl.handle.net/1811/31363

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Title: LIFETIME BROADENING IN THE ROTATIONALLY RESOLVED ELECTRONIC SPECTRA OF SOME FURAN DERIVATIVES AND ANALOGS IN THE GAS PHASE
Creators: Alvarez-Valtierra, Leonardo; Pratt, D. W.; Yi, John T.
Issue Date: 2007
Abstract: Fluorescence lifetimes of the electronic origin and some higher vibronic bands of dibenzofuran (DBF) }, (2006), 244302.} and dibenzothiophene (DBT) have been determined from the analyses of their rotationally resolved S$_1\leftarrow\,\,$S$_0$ fluorescence excitation spectra in the gas phase. A decrease by a factor of eight in the fluorescence lifetime has been observed for DBT with respect to DBF, where presumably the heavy atom effect plays a significant role in the intersystem crossing mechanism of these heterocycles. The high resolution spectra of the electronic origin transitions of two non-concatenated furan derivatives, 2,5-diphenylfuran (DPF) and 2,5-diphenyl-1,3,4-oxadioxole (DPO), exhibit similar lifetime broadening, about four times greater than that of DBF. Detailed information about radiationless transitions in the "statistical" limit will be discussed.
URI: http://hdl.handle.net/1811/31363
Other Identifiers: 2007-FD-05
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