Three D–D–π-A triphenylamine–coumarin sensitizers were designed and synthesized with a triphenylamine and coumarin double donor and a cyanoacrylic acid acceptor. Thiophene, bithiophene and phenylthiophene were used as π-bridges, respectively, and the effects of different π-bridges on the photophysical properties and photovoltaic performance were investigated. With the incorporation of an additional thiophene unit, the bithiophene π-bridge contributes to better light absorption and hence superior J_SC compared with the thiophene π-bridge. Although the dye with phenylthiophene π-bridge exhibits an inferior absorption spectrum to that with the thiophene π-bridge, it gives a photoelectrical conversion efficiency of 4.99% and exhibits the best photovoltaic performance of the three sensitizers, ascribed to its efficient photon-to-current conversion efficiency, slow charge recombination rate and good electron injection efficiency.

A series of new fluorinated quinoline analogs were synthesized using Tebufloquin as the lead compound, 2-fluoroaniline, ethyl 2-methylacetoacetate, and substituted benzoic acid as raw materials. Their structures were confirmed by ¹H NMR, ¹³C NMR, and HRMS. The compound 8-fluoro-2,3-dimethylquinolin-4-yl 4-(tert-butyl)benzoate (2b) was further determined by X-ray single-crystal diffraction. The antifungal activity was tested at 50 μg/mL, and the bioassay results showed that these quinoline derivatives had good antifungal activity. Among them, compounds 2b, 2e, 2f, 2k, and 2n exhibited good activity (>80%) against S. sclerotiorum, and compound 2g displayed good activity (80.8%) against R. solani.