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The complexes trans-[Fe(4-R-benacen)(CH3OH)N3], where 4-R-benacen2- are tetradentate open-chain N2O2-Schiff base N,N'-ethylenebis(4-R-benzoylacetoneiminato) ligands (R =H, Cl, Br,OCH3, CH3) are redox stable in the dark. Under the impact of ultraviolet and/or visible radiation they undergo photochemical reactions, yielding Fe(II) and formaldehyde CH2O as final products. As an intermediate, _CH2OH radicals were identified by EPR spin trapping technique. The efficiency of the photoredox processes, expressed by the quantum yield of Fe(II) formation, Fi Fe(II) is strongly wavelength dependent and influenced by the peripheral groups R of the tetradentate ligands. It was found, that along with a frequently observed decrease in the quantum yield with decreasing the photon energy of incident radiation (Fi Fe(II) at 313 nm < Fi Fe(II) at 366 nm
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1857--1865
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- Department of Inorganic Chemistry, Slovak Technical University,Radlinského 9, 81237 Bratislava, Slovakia
autor
- Department of Inorganic Chemistry, Slovak Technical University,Radlinského 9, 81237 Bratislava, Slovakia
Bibliografia
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Bibliografia
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bwmeta1.element.baztech-article-BUJ1-0024-0169