No abstract

Ultrafast pump−probe studies of room-temperature solutions of 3-hydroxyflavone (3-HF) and some 4‘-substituted derivatives have been undertaken. Transient absorption attributable to the two zwitterionic forms of the excited tautomer arising from excited-state intramolecular proton transfer (ESIPT) was observed across most of the visible spectral region. For 3-HF in methylcyclohexane and acetonitrile, the ESIPT was found to be so rapid that it was only possible to assign a time constant of 35 fs to the process. In ethanol, however, a time constant of 60 fs was determined. The slower ESIPT in this solvent was attributed to the greater strength of the solute−solvent interactions. For the derivatives of 3-HF in all three solvents, the ESIPT step was also found to be instrument-limited. In addition to the femtosecond kinetics, there was also a picosecond component of the kinetics that is attributed to ESPT in molecules that are intermolecularly hydrogen bonded to the solvent.

Donor–acceptor Stenhouse adducts (DASAs) are negative photochromes that hold great promise for a variety of applications. Key to optimizing their switching properties is a detailed understanding of the photoswitching mechanism, which, as yet, is absent. Here we characterize the actinic step of DASA-photoswitching and its key intermediate, which was studied using a combination of ultrafast visible and IR pump–probe spectroscopies and TD-DFT calculations. Comparison of the time-resolved IR spectra with DFT computations allowed to unambiguously identify the structure of the intermediate, confirming that light absorption induces a sequential reaction path in which a Z–E photoisomerization of C2–C3 is followed by a rotation around C3–C4 and a subsequent thermal cyclization step. First and second-generation DASAs share a common photoisomerization mechanism in chlorinated solvents with notable differences in kinetics and lifetimes of the excited states. The photogenerated intermediate of the second-generation DASA was photo-accumulated at low temperature and probed with time-resolved spectroscopy, demonstrating the photoreversibility of the isomerization process. Taken together, these results provide a detailed picture of the DASA isomerization pathway on a molecular level.

The triplet excited state properties of two BODIPY phenothiazine dyads (BDP-1 and BDP-2) with different lengths of linker and orientations of the components were studied. The triplet state formation of BODIPY chromophore was achieved via photoinduced electron transfer (PET) and charge recombination (CR). BDP-1 has a longer linker between the phenothiazine and the BODIPY chromophore than BDP-2. Moreover, the two chromophores in BDP-2 assume a more orthogonal geometry both at the ground and in the first excited state (87°) than that of BDP-1 (34-40°). The fluorescence of the BODIPY moiety was significantly quenched in the dyads. The charge separation (CS) and CR dynamics of the dyads were studied with femtosecond transient absorption spectroscopy (k = 2.2 × 10 s and 2 × 10 s for BDP-1 and BDP-2, respectively; k = 4.5 × 10 and 1.5 × 10 s for BDP-1 and BDP-2, respectively; in acetonitrile). Formation of the triplet excited state of the BODIPY moiety was observed for both dyads upon photoexcitation, and the triplet state quantum yield depends on both the linker length and the orientation of the chromophores. Triplet state quantum yields are 13.4 and 97.5% and lifetimes are 13 and 116 μs for BDP-1 and BDP-2, respectively. The spin-orbit charge transfer (SO-CT) mechanism is proposed to be responsible for the efficient triplet state formation. The dyads were used for triplet-triplet annihilation (TTA) upconversion, showing an upconversion quantum yield up to 3.2%.