Molecular design and synthesis of methoxy-substitued spiropyrans with photomodulated NIR-fluorescence

This study focuses on the molecular design and synthesis of salt spiropyrans with near-IR fluorescence. The structure of the obtained compounds was confirmed by NMR, IR and mass spectroscopy. In the course of studying the spectral and photoluminescent characteristics, it was possible to reveal the e...

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Veröffentlicht in:Photochemical & photobiological sciences 2023-11, Vol.22 (11), p.2651-2673
Hauptverfasser: Pugachev, Artem D., Kozlenko, Anastasia S., Makarova, Nadezhda I., Rostovtseva, Irina A., Ozhogin, Ilya V., Dmitriev, Vitaly S., Borodkin, Gennady S., Tkachev, Valery V., Utenyshev, Andrey N., Sazykina, Marina A., Sazykin, Ivan S., Azhogina, Tatiana N., Karchava, Shorena K., Klimova, Maria V., Metelitsa, Anatoly V., Lukyanov, Boris S.
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Sprache:eng
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Zusammenfassung:This study focuses on the molecular design and synthesis of salt spiropyrans with near-IR fluorescence. The structure of the obtained compounds was confirmed by NMR, IR and mass spectroscopy. In the course of studying the spectral and photoluminescent characteristics, it was possible to reveal the effect of some substituents in various positions on the properties of spiropyran dyes. Due to the structural similarity of one of the isomers to cyanine dyes, the obtained compounds are of interest as potential fluorescent probes for bioimagimg, in particular, for DNA studies. To reveal their ability of binding to DNA molecules molecular docking was carried out. Toxic effects of compounds demonstrating NIR fluorescence were studied on biofilms, as well as using bacterial lux-biosensors. Graphical abstract
ISSN:1474-905X
1474-9092
DOI:10.1007/s43630-023-00479-1