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The S2→S1 fluorescence of azulene in a naphthalene mixed crystal has been measured from 740 to 1000 nm at 4.2 K. Of the 25 in-plane fundamentals (exclusive of C–H stretches) of the S1 state, 20 are readily identifiable in emission. A number of other bands are present in the spectrum and these are tentatively identified as S1 out-of-plane vibrations induced by vibronic coupling to σπ* and/or πσ* excited electronic states. An emission previously assigned as T1→S0 phosphorescence is shown to be a combination band of S2→S1 fluorescence. The branching ratio of S2 →S0 fluorescence to S2→S1 fluorescence is approximately 7500 for xenon arc lamp excitation; this is an order of magnitude larger than the value reported for short pulse laser excitation. A summary of photophysical parameters for the low-lying electronic states of azulene, based on the most recent and reliable experimental data, is also presented.
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Gillispie et al. (1978) studied this question.
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