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Trapping of a Highly Reactive Oxoiron(IV) Complex in the Catalytic Epoxidation of Olefins by Hydrogen Peroxide
15
Citations
38
References
2019
Year
Chemical EngineeringEngineeringAlkene MetathesisBiochemistryNatural SciencesFe IvOrganic ChemistryHighly Reactive OxoironOrganometallic CatalysisCatalysisRedox ChemistryChemistryDeoxygenationCatalytic EpoxidationRedox BiologyHydrogen PeroxideNonheme OxoironCatalytic Synthesis
Abstract The generation of a nonheme oxoiron(IV) intermediate, [(cyclam)Fe IV (O)(CH 3 CN)] 2+ ( 2 ; cyclam=1,4,8,11‐tetraazacyclotetradecane), is reported in the reactions of [(cyclam)Fe II ] 2+ with aqueous hydrogen peroxide (H 2 O 2 ) or a soluble iodosylbenzene ( s PhIO) as a rare example of an oxoiron(IV) species that shows a preference for epoxidation over allylic oxidation in the oxidation of cyclohexene. Complex 2 is kinetically and catalytically competent to perform the epoxidation of olefins with high stereo‐ and regioselectivity. More importantly, 2 is likely to be the reactive intermediate involved in the catalytic epoxidation of olefins by [(cyclam)Fe II ] 2+ and H 2 O 2 . In spite of the predominance of the oxoiron(IV) cores in biology, the present study is a rare example of high‐yield isolation and spectroscopic characterization of a catalytically relevant oxoiron(IV) intermediate in chemical oxidation reactions.
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