Fused-ring derivatives of quinoxalines: Spectroscopic characterization and photoinduced processes investigated by EPR spin trapping technique

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Abstract

10-Ethyl-7-oxo-7,10-dihydropyrido[2,3-f]quinoxaline derivatives, synthesized as promising biologically/photobiologically active compounds were characterized by UV/vis, FT-IR and fluorescent spectroscopy. Photoinduced processes of these derivatives were studied by EPR spectroscopy, monitoring in situ the generation of reactive intermediates upon UVA (λmax = 365 nm) irradiation. The formation of reactive oxygen species and further oxygen- and carbon-centered radical intermediates was detected and possible reaction routes were suggested. To quantify the investigated processes, the quantum yields of the superoxide radical anion spin-adduct and 4-oxo-2,2,6,6-tetramethylpiperidine N-oxyl generation were determined, reflecting the activation of molecular oxygen by the excited state of the quinoxaline derivative. © 2014 by the authors.

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Barbieriková, Z., Dvoranová, D., Bella, M., Milata, V., Czímerová, A., & Brezová, V. (2014). Fused-ring derivatives of quinoxalines: Spectroscopic characterization and photoinduced processes investigated by EPR spin trapping technique. Molecules, 19(8), 12078–12098. https://doi.org/10.3390/molecules190812078

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