Investigating the Synergistic Influence of Redox‐Inactive Metal Ions at the Secondary Coordination Sphere of Non‐Heme Iron Complexes on Oxygen Reduction Reaction

The secondary coordination sphere (SCS) around the substrate binding site of a catalyst, such as a proton relay, formation of a hydrogen bonding network, and electrostatic effects, plays a critical role in controlling the selectivity and rate of oxygen reduction reaction (ORR). Herein, we report the ORR study of a series of FeIII complexes having a uniform primary coordination sphere and an unlike SCS. The Fe(III) complex, lacking any secondary coordination sphere (SCS) modifications, exhibited slow oxygen reduction reaction (ORR) kinetics in the presence of decamethylferrocene (Fc*) and trifluoroacetic acid (TFAH) in oxygen-saturated acetonitrile. The presence of redox-inactive metal ions (Mn+), such as Mg2+ and Ca2+, at SCS enhances the ORR rate, which can be attributed to the presence of the electrostatic effect created by these Mn+ ions. Strikingly, no benign effect was noticed when Sr2+, Ba2+, Y3+, and Nd3+ were present at the SCS. Interestingly, all the Fe complexes revealed catalytic H2O2 disproportionation and H2O2 reduction reaction (H2O2RR). The study highlights the importance of modifying the SCS on the ORR and H2O2RR by a series of molecular non-heme Fe(III) complexes.