Styrylbenzoquinoline dyads as a new type of fluorescing photochromes operating via [2 + 2] photocycloaddition mechanism: Optimization of the structure.

We synthesized and studied a novel bichromophoric dyad in which bridging methylene groups link two styrylbenzo[f]quinoline (SBQ) photochromes to a salicylic acid residue. The dyad was designed for use as a fluorescent P-type photochrome acting via a [2 + 2] photocycloaddition (PCA) reaction. Compared to previously studied dyads, a change in the attachment handle and shortening of the bridging groups resulted in simultaneous rise of the quantum yields of both fluorescence and PCA.

[2+2] Photocycloaddition in a bichromophoric dyad: photochemical concerted forward reaction following Woodward-Hoffmann rules and photoinduced stepwise reverse reaction of the ring opening predissociation.

A novel biphotochromic dyad with styrylbenzo[]quinoline photochromes was designed and synthesized to study the [2+2] photocycloaddition (PCA) reaction leading to cyclobutane with two benzo[]quinoline (BQ) substituents and the reverse four-membered ring opening reaction. In the dyad, PCA occurs in a concerted manner according to the Woodward-Hoffmann rules in the ππ* excited state after excitation of the whole conjugated π-system comprising the ethylene group. Nanosecond time-resolved emission spectroscopy indicated formation of an excimer as a possible intermediate of the PCA reaction.

Oxidative C-H/C-H Coupling of Dipyrromethanes with Azines by TiO-Based Photocatalytic System. Synthesis of New BODIPY Dyes and Their Photophysical and Electrochemical Properties.

Oxidative C-H/C-H coupling reactions of dipyrromethanes with azines in the presence of a heterophase oxidative photocatalytic system (O/TiO/visible light irradiation) were carried out. As a result of cyclization of obtained compounds with boron trifluoride etherate, new hetaryl-containing derivatives of 4,4-difluoro-4-boron-3,4-diaza--indacene were synthesized. For the obtained compounds, absorption and luminescence spectra, quantum yields of luminescence as well as cyclic volt-amperograms were measured.

Fluorescence from 3,5-diphenyl-8-CF-BODIPYs with amino substituents on the phenyl rings: Quenching by aromatic molecules.

The photoluminescence from n-hexane solutions of the dyes obtained by the introduction of amino groups into the meta position of the phenyl rings of 3,5-diphenyl-8-CF-BODIPY was found to be strongly quenched by some aromatic molecules (benzene and toluene). On the contrary, the introduction of an amino group into the para position does not lead to significant quenching. The quenching of photoluminescence from the meta derivatives obeys the mixed static + dynamic mechanism.

Studying the size-selective precipitation of colloidal quantum dots by decomposing the excitation-emission matrix.

The exciton peak in the excitation-emission matrix (EEM) of colloidal quantum dots implicitly contains information about inhomogeneous broadening and the photoluminescence (PL) and photoluminescence excitation (PLE) spectra of individual particles in the vicinity of the absorption onset. A numerical procedure for extracting this information has been developed and applied to the EEMs of polydisperse InP/ZnS core/shell colloidal quantum dots and their supernatant solutions obtained by partial precipitation with a non-solvent. The inhomogeneous broadenings obtained in this way have been converted by the sizing curve into particle-size distributions.