Journal
CHEMPHOTOCHEM
Volume 5, Issue 4, Pages 296-297Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cptc.202100065
Keywords
dibenzophenazine; excited states; quantum chemistry; time-resolved spectroscopy; transient absorption
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Funding
- EUs Horizon 2020 OCTA project [778158]
- Deutsche Forschungsgemeinschaft [396890929/GRK 2482]
- Strategic Research Fund of the HHU Dusseldorf
- MEXT (Ministry of Education, Culture, Science and Technology, Japan) [JP15H00997, JP17H05155, JP19H05716]
- Japan Prize Foundation
- Asahi Glass Foundation
- Mitsubishi Foundation
- Deutsche Forschungsgemeinschaft (DFG) [INST 208/704-1 FUGG]
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The photophysics of DBPHZ in solution was studied through spectroscopic methods, showing that the solvent type has weak effects on the photophysical properties. The first excited singlet state has a short lifetime and moderate fluorescence yield, while the lowest triplet state is populated with higher yields. Quantum chemical computations suggest an efficient intersystem crossing mechanism towards the triplet manifold.
The photophysics of dibenzo[a,j]phenazine (DBPHZ) in solution was investigated by steady-state and time-resolved spectroscopy. The nature of the solvent (methanol, acetonitrile, dichloromethane and cyclohexane were considered) only weakly affects the photophysical properties. The first excited singlet state features a lifetime of the order of 1 ns. Its fluorescence emission is centered around 420 nm and occurs with moderate yields of approximate to 0.1. The lowest triplet state is populated with yields of approximate to 0.3. Quantum chemical computations suggest that a 3n pi* state energetically close to the primarily excited singlet state is responsible for the efficient intersystem crossing towards the triplet manifold.
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