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Abstract: From both steady state and fluorescence lifetime measurements it reveals that due to photoexcitation of benzotriazole (BZ) part of the bichromophore, 9(1-H-benzotriazole-lylmethyl)-9H-carbazole (BHC), singlet–singlet energy transfer takes place to populate the lowest excited singlet of carbazole (CZ). CZ, thus being excited indirectly via energy transfer process, undergoes strong charge transfer (CT) reaction with the surrounding polar medium acetonitrile (ACN). On the other hand, very weak CT band was apparent when CZ part, within BHC, was directly excited. In less polar tetrahydrofuran (THF) and polar benzonitrile (BN) environment, lack of formation of CT band strongly suggests in favor of the electron-accepting behavior of ACN. Moreover, by measuring the emission spectra of BHC in microcrystals and of 30 bilayers mixed LB film at high mole fraction of BHC molecules, the possibility of excimer formation or aggregation has been ruled out. Thus, BHC, when dissolved in ACN, acts as a triad system of BZ–CZ–ACN where BZ acts as an antenna molecule and CZ as a reaction center. The possible role of the bichromophoric system BHC as an artificial photosynthetic or solar energy conversion device has been hinted. [Copyright &y& Elsevier]

The photophysical properties and the nature of the photoinduced electron transfer (PET) reactions within a synthesized anisole (A)−thioindoxyl (T) dyad system (24MBTO) have been studied by electrochemical, steady-state, and time-resolved spectroscopic techniques. Computations on the dyad were performed both in gas phase as well as solvent environment by TD-DFT method with B3LYP density function. The geometry optimization calculation of 24MBTO was done by 6−311G(d,p) basis function set implemented in the Gaussian package. The theoretical values of singlet vertical excitation energies were found to correlate well with the experimentally observed ones. The electrochemical measurements indicate the possibility of occurrence of PET reactions within 24MBTO between the linked redox centers A and T. Both steady-state and time-resolved spectroscopic measurements on the novel synthesized 24MBTO dyad demonstrate the formations of the two types of isomeric species:  Z- and E- forms, resulted from the charge separation reactions. From the detailed studies it reveals that the present thioaurone may behave as a versatile photoswitchable system. It has been hinted that the loss process (charge recombination) within 24MBTO could possibly be prevented by incorporating it within the hydrophobic cavity of -cyclodextrin (CD). [ABSTRACT FROM AUTHOR]