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Article Dans Une Revue Molecules Année : 2022

Weak coordinating character of organosulfonates in oriented silica films: an efficient approach for immobilizing cationic metal-transition complexes

Résumé

Iron (II) tris(2,2′-bipyridine) complexes, [Fe(bpy)3]2+, have been synthesized and immobilized in organosulfonate-functionalized nanostructured silica thin films taking advantage of the stabilization of [Fe(H2O)6]2+ species by hydrogen bonds to the anionic sulfonate moieties grafted to the silica nanopores. In a first step, thiol-based silica films have been electrochemically generated on indium tin oxide (ITO) substrates by co-condensation of 3-mercaptopropyltrimethoxysilane (MPTMS) and tetraethoxysilane (TEOS). Secondly, the thiol function has been modified to sulfonate by chemical oxidation using hydrogen peroxide in acidic medium as an oxidizing agent. The immobilization of [Fe(bpy)3]2+ complexes has been performed in situ in two consecutive steps: (i) impregnation of the sulfonate functionalized silica films in an aqueous solution of iron (II) sulfate heptahydrate; (ii) dipping of the iron-containing mesostructures in a solution of bipyridine ligands in acetonitrile. The in situ formation of the [Fe(bpy)3]2+ complex is evidenced by its characteristic optical absorption spectrum, and elemental composition analysis using X-ray photoelectron spectroscopy. The measured optical and electrochemical properties of immobilized [Fe(bpy)3]2+ complexes are not altered by confinement in the nanostructured silica thin film.
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hal-03796349 , version 1 (04-10-2022)

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Samuel Ahoulou, Clara Richart, Cédric Carteret, Sébastien Pillet, Neus Vilà, et al.. Weak coordinating character of organosulfonates in oriented silica films: an efficient approach for immobilizing cationic metal-transition complexes. Molecules, 2022, 27 (17), pp.5444. ⟨10.3390/molecules27175444⟩. ⟨hal-03796349⟩
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