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We have generated a high-spin Fe(III)-OOH complex supported by tetramethylcyclam via protonation of its conjugate base and characterized it in detail using various spectroscopic methods. This Fe(III)-OOH species can be converted quantitatively to an Fe(IV)═O complex via O-O bond cleavage; this is the first example of such a conversion. This conversion is promoted by two factors: the strong Fe(III)-OOH bond, which inhibits Fe-O bond lysis, and the addition of protons, which facilitates O-O bond cleavage. This example provides a synthetic precedent for how O-O bond cleavage of high-spin Fe(III)-peroxo intermediates of non-heme iron enzymes may be promoted.

Characterization of a High-Spin Non-Heme FeIII–OOH Intermediate and Its Quantitative Conversion to an FeIV═O Complex

Characterization of a High-Spin Non-Heme Fe^III–OOH Intermediate and Its Quantitative Conversion to an Fe^IV═O Complex