Mechanism of deactivation processes of excited iron(III) thiocyanato complexes with benacen‐type ligands

Abstract

The complexes [Fe(4-R-benacen)(CH3OH)(NCS)], where 4-R-benacen2−are tetradentate open-chainN,N′-ethylenebis(4-R-benzoylacetoneiminato)N2O2-ligands (R=H, Cl, Br,OCH3), are redox stable in the dark in methanolic solutions. Irradiation of the complexes into intraligand and/or ligand-to-metal charge-transfer bands induces a series of photophysical and photochemical deactivation processes leading to Fe(II) andCH2Oas final products in a2:1molar ratio. Formation of polystyrene containing bonded NCS group when irradiating the complexes in the presence of styrene monomer used as a radical scavenger indicates that the primary photoreduction of Fe(III) to Fe(II) is accompanied by the oxidation of NCS−ligand to•NCS radical. 4-R-benacen-ligands behave as an innocent moiety virtually not participating in the photoinduced redox processes. The quantum yield of Fe(II) formationΦFe(II)decreases significantly with increased wavelength of the incident radiation, and is slightly influenced by the peripheral groups R of the 4-R-benacen-ligands.