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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >Lifetime Broadening in the Rotationally Resolved Electronic Spectra of Dibenzothiophene,2,5-Diphenylfuran, and 2,5-Diphenyl-1,3,4-oxadiazole in the Gas Phase. IntersystemCrossing Dynamics in the Statistical Limit
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Lifetime Broadening in the Rotationally Resolved Electronic Spectra of Dibenzothiophene,2,5-Diphenylfuran, and 2,5-Diphenyl-1,3,4-oxadiazole in the Gas Phase. IntersystemCrossing Dynamics in the Statistical Limit

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The fluorescence lifetime of the zero point vibrational level of the first excited electronic state ofdibenzothiophene (DBT) has been determined to be 1.0 ns by analysis of its rotationally resolved S1 r S0fluorescence excitation spectrum. The S1 lifetime of DBT is substantially shorter than those observed forfluorene (FLU), carbazole (CAR), and dibenzofuran (DBF), analogs of DBT in which the heavy sulfur atomis replaced by lighter ones. The electronic origin bands through the series CAR, FLU, DBF, and DBT exhibita monotonic increase in Lorentzian broadening in their Voigt line shape profiles. Two other heterocyclicmolecules manifest similar photophysical properties; 2,5-diphenylfuran and 2,5-diphenyl-1,3,4-oxadiazole.Lorentzian line shape broadenings of - 76 MHz were observed in the high-resolution spectra of their originbands. Possible reasons for the short fluorescence lifetimes of these heterocycles are discussed.

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