Journal article
Directing a Non-Heme Iron(III)-Hydroperoxide Species on a Trifurcated Reactivity Pathway
The reactivity of [FeIII(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 H2O2 and presence or absence of sacrificial substrates. The outcome can be switched between: 1)catalysed H2O2 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)FeIIIO-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 FeIII/FeII redox potentials for the pro-catalysts.
Language: | English |
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Year: | 2018 |
Pages: | 5134-5145 |
ISSN: | 15213765 and 09476539 |
Types: | Journal article |
DOI: | 10.1002/chem.201704615 |
ORCIDs: | 0000-0002-6034-453X , 0000-0001-5063-6961 , 0000-0001-5587-0626 and Frandsen, Cathrine |