A high-spin alkylperoxo-iron(iii) complex with cis -anionic ligands: implications for the superoxide reductase mechanism.

The N 3 O macrocycle of the 12-TMCO ligand stabilizes a high spin ( S = 5/2) [Fe III (12-TMCO)(OO t Bu)Cl] + (3-Cl) species in the reaction of [Fe II (12-TMCO)(OTf) 2 ] (1-(OTf) 2 ) with tert -butylhydroperoxide ( t BuOOH) in the presence of tetraethylammonium chloride (NEt 4 Cl) in acetonitrile at -20 °C. In the absence of NEt 4 Cl the oxo-iron(iv) complex 2 [Fe IV (12-TMCO)(O)(CH 3 CN)] 2+ is formed, which can be further converted to 3-Cl by adding NEt 4 Cl and t BuOOH. The role of the cis -chloride ligand in the stabilization of the Fe III -OO t Bu moiety can be extended to other anions including the thiolate ligand relevant to the enzyme superoxide reductase (SOR). The present study underlines the importance of subtle electronic changes and secondary interactions in the stability of the biologically relevant metal-dioxygen intermediates. It also provides some rationale for the dramatically different outcomes of the chemistry of iron(iii)peroxy intermediates formed in the catalytic cycles of SOR (Fe-O cleavage) and cytochrome P450 (O-O bond lysis) in similar N 4 S coordination environments.