A series of water-soluble sodium salts of 3-formyl-4-hydroxybenzenesulfonic acid thiosemicarbazones (or sodium 5-sulfonate-salicylaldehyde thiosemicarbazones) containing different substituents at the terminal nitrogen atom (H, Me, Et, Ph) and their copper(II) complexes have been prepared and characterised by elemental analysis, spectroscopic techniques (IR, UV-vis, ¹H NMR), ESI mass spectrometry, X-ray crystallography and cyclic voltammetry. The proligands and their copper(II) complexes exhibit moderate water solubility and good stability in aqueous environment, determined by investigating their proton dissociation and complex formation equilibria. The copper(II) complexes showed moderate anticancer activity in established human cancer cell lines, while the proligands were devoid of cytotoxicity. The anticancer activity of the copper(II) complexes correlates with their ability to induce ROS accumulation in cells, consistent with their redox potentials within the biological window, triggering the activation of antioxidation defense mechanisms in response to the ROS insult. These studies pave the way for the investigation of ROS-inducing copper(II) complexes as prospective antiproliferative agents in cancer chemotherapy.

Investigation of the cytotoxic potential of imidazole-derived thiosemicarbazones and their copper( ii ) complexes with CHCl ₂ CO ₂ ⁻ as a co-ligand.

X- and Q-band electron paramagnetic resonance (EPR) spectroscopy was used to characterize polycrystalline Cu(II) complexes that contained sodium 5-sulfonate salicylaldehyde thiosemicarbazones possessing a hydrogen, methyl, ethyl, or phenyl substituent at the terminal nitrogen. The ability of thiosemicarbazone proligands to generate superoxide radical anions and hydroxyl radicals upon their exposure to UVA irradiation in aerated aqueous solutions was evidenced by the EPR spin trapping technique. The UVA irradiation of proligands in neutral or alkaline solutions and dimethylsulfoxide (DMSO) caused a significant decrease in the absorption bands of aldimine and phenolic chromophores. Mixing of proligand solutions with the equimolar amount of copper(II) ions resulted in the formation of 1:1 Cu(II)-to-ligand complex, with the EPR and UV-Vis spectra fully compatible with those obtained for the dissolved Cu(II) thiosemicarbazone complexes. The formation of the complexes fully inhibited the photoinduced generation of reactive oxygen species, and only subtle changes were found in the electronic absorption spectra of the complexes in aqueous and DMSO solutions upon UVA steady-state irradiation. The dark redox activity of copper(II) complexes and proligand/Cu(II) aqueous solutions towards hydrogen peroxide which resulted in the generation of hydroxyl radicals, was confirmed by spin trapping experiments.

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.

A new method to functionalize layered simple hydroxides by post-synthesis modification is described. A layered cobalt hydroxide was modified with a molecule bearing a free amino group. We show here that it is possible to post-functionalize the metal hydroxide layers by performing in situ microwave assisted reactions with the free amino group, constituting a new appealing strategy for functionalization of layered solids. The obtained compounds are characterized by ancillary techniques and their magnetic properties were investigated, which show that the inorganic magnetic layers are not deeply affected by the post-functionalization process.

We report on the vacuum thermal deposition of bilayer thin films of the luminescent complex Ir(ppy)₃, tris[2-phenylpyridinato-C2,N]iridium(III), and the spin crossover complex [Fe(HB(tz)₃)₂], bis[hydrotris(1,2,4-triazol-1-yl)borate]iron(II). Switching the spin state of iron ions from the low spin to the high spin state around 337 K leads to a reversible jump of the luminescence intensity, while the spectrum shape and the luminescence lifetime remain unchanged. The luminescence modulation occurs due to the different UV light absorption properties of the iron complex in the two spin states and its magnitude can therefore be precisely adjusted by varying the film thickness. These multilayer luminescence switches hold potential for micro- and nanoscale thermal sensing and imaging applications.