Comparing the Thermodynamic Properties and Reactivity of Fe III - and Mn III –Hydroxo Complexes

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.