Intramolecular C–H and C–F Bond Oxygenation Mediated by a Putative Terminal Oxo Species in Tetranuclear Iron Complexes

Herein we report the intramolecular arene C–H and C–F bond oxygenation by tetranuclear iron complexes. Treatment of [LFe₃(PhPz)₃OFe]­[OTf]₂ (1) or its fluorinated analog [LFe₃(F₂ArPz)₃OFe]­[OTf]₂ (5) with iodosobenzene results in the regioselective hydroxylation of a bridging pyrazolate ligand, converting a C–H or C–F bond into a C–O bond. The observed reactivity suggests the formation of terminal and reactive Fe-oxo intermediates. With the possibility of intramolecular electron transfer within clusters in 1 and 5, different reaction pathways (Fe^IV-oxo vs Fe^III-oxo) might be responsible for the observed arene hydroxylation.