New fluorescent molecular rotors (FMRs) were developed by modification of the Thioflavin T (ThT) structure via introduction of methyl and methoxy groups. Effects of the substituents on fluorescence properties and twisted intramolecular charge transfer (TICT) rate in the excited state of the molecules were studied using steady-state fluorescence and time-resolved absorption spectroscopy. Quantum chemical calculations of the molecules in the ground and excited states were carried out to aid interpretation of the experimental results. Only cationic forms of ThT derivatives have FMR properties and exhibit viscosity-dependent fluorescence. The TICT rate was found to be affected by the size of the molecular fragments, which experience mutual rotation, dihedral angle [Formula: see text] between the fragments in the ground state as well as their donor/acceptor properties.
An analysis of the results of complex experimental and theoretical studies of photoinduced changes in the spectral properties of photochromic diarylethene in various nanostructured systems is presented. The properties of diarylethene were studied in solutions in the presence of colloidal metal and semiconductor nanoparticles, as well as in the form of solid-phase composite nanostructured core-shell systems based on colloidal nanoparticles with a shell of diarylethene molecules (including in a polymer matrix). A photoinduced reversible change in the electronic and vibrational spectra of diarylethene in various studied matrices was found. The results can be used to create optoelectronic photo-switchable elements for ultra-high-capacity memory devices, photo-controlled molecular switches and sensors. Keywords: photochromism, diarylethenes, nanocomposites, quantum dots, electronic spectra, vibrational spectra, fluorescence, Ferster resonance energy transfer, quantum chemical calculations.
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