The radical intermediates formed upon UVA irradiation of titanium dioxide suspensions in aqueous and non-aqueous environments were investigated applying the EPR spin trapping technique. The results showed that the generation of reactive species and their consecutive reactions are influenced by the solvent properties (e.g., polarity, solubility of molecular oxygen, rate constant for the reaction of hydroxyl radicals with the solvent). The formation of hydroxyl radicals, evidenced as the corresponding spin-adducts, dominated in the irradiated TiO₂ aqueous suspensions. The addition of ¹⁷O-enriched water caused changes in the EPR spectra reflecting the interaction of an unpaired electron with the ¹⁷O nucleus. The photoexcitation of TiO₂ in non-aqueous solvents (dimethylsulfoxide, acetonitrile, methanol and ethanol) in the presence of 5,5-dimethyl-1-pyrroline N-oxide spin trap displayed a stabilization of the superoxide radical anions generated via electron transfer reaction to molecular oxygen, and various oxygen- and carbon-centered radicals from the solvents were generated. The character and origin of the carbon-centered spin-adducts was confirmed using nitroso spin trapping agents.

The g-C₃N₄/TiO₂ nanopowders prepared by the annealing of melamine and TiO₂ P25 at 550 °C were investigated under dark and upon UV or visible-light photoactivation using X- and Q-band electron paramagnetic resonance (EPR) spectroscopy. The EPR spectra of powders monitored at room temperature and 100 K showed the impact of the initial loading ratio of melamine/TiO₂ on the character of paramagnetic centers observed. For the photocatalysts synthesized using a lower titania content, the paramagnetic signals characteristic for the g-C₃N₄/TiO₂ nanocomposites were already found before exposure. The samples annealed using the higher TiO₂ loading revealed the photoinduced generation of paramagnetic nitrogen bulk centers (g-tensor components g₁ = 2.005, g₂ = 2.004, g₃ = 2.003 and hyperfine couplings from the nitrogen A₁ = 0.23 mT, A₂ = 0.44 mT, A₃ = 3.23 mT) typical for N-doped TiO₂. The ability of photocatalysts to generate reactive oxygen species (ROS) upon in situ UV or visible-light photoexcitation was tested in water or dimethyl sulfoxide by EPR spin trapping using 5,5-dimethyl 1-pyrroline N-oxide. The results obtained reflect the differences in photocatalyst nanostructures caused by the differing initial ratio of melamine/TiO₂; the photocatalyst prepared by the high-temperature treatment of melamine/TiO₂ wt. ratio of 1:3 revealed an adequate photoactivity in both spectral regions.

Graphitic carbon nitride (g-C₃N₄) is a conjugated polymer, which recently drew a lot of attention as a metal-free and UV and visible light responsive photocatalyst in the field of solar energy conversion and environmental remediation. This is due to its appealing electronic band structure, high physicochemical stability and earth-abundant nature. In the present work, bulk g-C₃N₄ was synthesized by thermal decomposition of melamine. This material was further exfoliated by thermal treatment. S-doped samples were prepared from thiourea or further treatment of exfoliated g-C₃N₄ by mesylchloride. Synthesized materials were applied for photocatalytic removal of air pollutants (acetaldehyde and NO_x) according to the ISO 22197 and ISO 22197-1 methodology. The efficiency of acetaldehyde removal under UV irradiation was negligible for all g-C₃N₄ samples. This can be explained by the fact that g-C₃N₄ under irradiation does not directly form hydroxyl radicals, which are the primary oxidation species in acetaldehyde oxidation. It was proved by electron paramagnetic resonance (EPR) spectroscopy that the dominant species formed on the irradiated surface of g-C₃N₄ was the superoxide radical. Its production was responsible for a very high NO_x removal efficiency not only under UV irradiation (which was comparable with that of TiO₂), but also under visible irradiation.

A series of four water-soluble salicylaldehyde thiosemicarbazones with a positively charged trimethylammonium moiety ([H₂L^R]Cl, R = H, Me, Et, Ph) and four copper(II) complexes [Cu(HL^R)Cl]Cl (1–4) were synthesised with the aim to study (i) their antiproliferative activity in cancer cells and, (ii) for the first time for thiosemicarbazones, the interaction with membrane transport proteins, specifically organic cation transporters OCT1–3. The compounds were comprehensively characterised by analytical, spectroscopic and X-ray diffraction methods. The highest cytotoxic effect was observed in the neuroblastoma cell line SH-5YSY after 24 h exposure and follows the rank order: 3 > 2 > 4 > cisplatin > 1 >> [H₂L^R]Cl. The copper(II) complexes showed marked interaction with OCT1–3, comparable to that of well-known OCT inhibitors (decynium 22, prazosin and corticosterone) in the cell-based radiotracer uptake assays. The work paves the way for the development of more potent and selective anticancer drugs and/or OCT inhibitors.

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 (λ_max = 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.