Abstract
We report the first observation of thermally activated delayed fluorescence (TDF) from an excited-state intramolecular proton-transfer (ESIPT) molecule, a hydroxyl-substituted tetraphenyl imidazole derivative (HPI-Ac), in degassed solutions as well as in low-temperature organic matrixes. In the absence of oxygen, the blue emission of an identical spectral feature was observed in the nanosecond ( approximately 4.4 ns) and microsecond ( approximately 25 micros) time domains, and the fluorescence intensity increased with temperature. From the temperature dependence of the time-resolved spectra of HPI-Ac, the energy gap between the first-excited singlet state and the lowest triplet state was determined to be 7.6 +/- 0.3 kJ/mol (630 +/- 25 cm-1), and the limiting rate constant of intrinsic reverse intersystem crossing was estimated to be 1.3 (+/-0.5) x 107 s-1.
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