Comparison reveals Fe hydroxo complex oxidizes 10-fold slower than Mn hydroxo in PCET reactions, indicating metal identity impact.
Mononuclear FeIII- and MnIII-hydroxo units are involved in proton-coupled electron-transfer (PCET) reactions in the lipoxygenase enzymes. While Fe and Mn forms of these enzymes utilize nearly identical active sites, there exist few synthetic model complexes where FeIII- and MnIII-hydroxo species share the same coordination sphere. In this work, we generated the FeIII-hydroxo complex [FeIII(OH)(dpaq)]⁺ (2) from the previously reported FeIII-aqua complex [FeIII(OH₂)(dpaq)]²⁺ (1) by base titration in both CH₃CN and H₂O. Although the FeIII-aqua complex is low-spin (S = 1/2), X-band EPR data (g = 8.4 and 4.3) and a room-temperature solution magnetic moment (5.90 μB in CD₃CN) indicate that 2 is high spin (S = 5/2). From additional experiments, we determined O-H BDFEs for the FeII-aqua complex in CH₃CN (62.5 kcal mol⁻¹) and in H₂O (62.1 kcal mol⁻¹). These values are 15 kcal mol⁻¹ lower than the O-H BDFE of the analogous MnII-aqua complex, [MnII(OH₂)(dpaq)]⁺, in CH₃CN, highlighting a reduced oxidizing capability of the FeIII-hydroxo species in PCET reactions. Comparative kinetic studies with 1,2-diphenylhydrazine reveal that 2 oxidizes this substrate 10-fold slower than the MnIII-hydroxo analogue. These results show how metal identity affects the thermodynamics and reactivity of PCET by metal(III)-hydroxo complexes at parity of coordination sphere.
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Puthiyadath et al. (2025) studied this question.
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