Coumarin-pyridine push-pull fluorophores: Synthesis and photophysical studies.

[Display omitted] • Coumarin-pyridine fluorophores were obtained via C-H functionalization and Boger reaction. • 4-Alkylcoumarin fluorophores have emission and absorption maxima at 402–415 and 210–307 nm, respectively. • Obtained 4-alkylcoumarin fluorophores are characterized by quantum yields of 6–19%. • Derivatives of 4-phenylcoumarin did not exhibit any noticeable fluorescence. A series of coumarin-pyridine-based push-pull fluorophores were prepared starting from 1,2,4-triazines by using direct C-H functionalization (S N H-reaction)–Diels-Alder–retro Diels-Alder domino reaction sequence. This efficient synthetic strategy allowed to obtain a series of 19 coumarin-pyridine fluorophores. Their photophysical properties were studied. While pyridine-substituted derivatives of 4-alkylcoumarins may be considered as alternative to coumarin dyes characterized by emission maxima mainly in a visible region with wavelengths of 402–415 nm, absorption in the UV range at 210–307 nm, and good photoluminescence quantum yields of 6–19%, all the derivatives of 4-phenylcoumarin did not exhibit any noticeable fluorescence. More detailed photophysical studies were carried out for two the most representative derivatives of 4-alkyl-coumarin-pyridines to demonstrate their positive solvatochromism, and the collected data were analyzed by using Lippert-Mataga equation, as well as Kosower and Dimroth/Reichardt scales. The obtained results demonstrate that the combining two chromophore systems, such as 2,5-diarylpyridine and coumarin ones, is promising in terms of improving the photophysical properties of the new coumarin-pyridine hybrid compounds. [ABSTRACT FROM AUTHOR]