1. Directing a Non-Heme Iron(III)-Hydroperoxide Species on a Trifurcated Reactivity Pathway
- Author
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Wesley R. Browne, Christina Wegeberg, Christine J. McKenzie, Cathrine Frandsen, Frants Roager Lauritsen, Steen Mørup, and Molecular Inorganic Chemistry
- Subjects
N,O ligands ,Denticity ,High-valent iron ,AMINOPYRIDYL LIGANDS ,OXYGEN ACTIVATION ,Disproportionation ,OXIDATION ,010402 general chemistry ,Photochemistry ,01 natural sciences ,Peroxide ,Medicinal chemistry ,Redox ,Aldehyde ,H O activation ,Catalysis ,peroxides ,chemistry.chemical_compound ,O ligands ,high-valent iron ,FE-III-OOH ,H2O2 activation ,Carboxylate ,iron(IV) ,COORDINATION SPHERE ,chemistry.chemical_classification ,hydroxyl radical ,RESONANCE RAMAN ,010405 organic chemistry ,Ligand ,MODEL COMPLEXES ,Organic Chemistry ,General Chemistry ,0104 chemical sciences ,ROOM-TEMPERATURE ,chemistry ,ACTIVE-SITES ,DIOXYGEN ACTIVATION - Abstract
The reactivity of [Fe III(tpena)] 2+ (tpena=N,N,N′-tris(2-pyridylmethyl)ethylenediamine-N′-acetate) as a catalyst for oxidation reactions depends on its ratio to the terminal oxidant H 2O 2 and presence or absence of sacrificial substrates. The outcome can be switched between: 1) catalysed H 2O 2 disproportionation, 2) selective catalytic oxidation of methanol or benzyl alcohol to the corresponding aldehyde, or 3) oxidative decomposition of the tpena ligand. A common mechanism is proposed involving homolytic O−O cleavage in the detected transient purple low-spin (S=1/2) [(tpenaH)Fe IIIO−OH] 2+. The resultant iron(IV) oxo and hydroxyl radical both participate in controllable hydrogen-atom transfer (HAT) reactions. Consistent with the presence of a weaker σ-donor carboxylate ligand, the most pronounced difference in the spectroscopic properties of [Fe(OOH)(tpenaH)] 2+ and its conjugate base, [Fe(OO)(tpenaH)] +, compared to non-heme iron(III) peroxide analogues supported by neutral multidentate N-only ligands, are slightly blue-shifted maxima of the visible absorption band assigned to ligand-to-metal charge-transfer (LMCT) transitions and, corroborating this, lower Fe III/Fe II redox potentials for the pro-catalysts.
- Published
- 2017
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