Enhanced Four‐Electron Oxygen Reduction Selectivity of Clamp‐Shaped Cobalt(II) Porphyrin(2.1.2.1) Complexes

Abstract

The molecular structure, electrochemistry, spectroelectrochemistry and electrocatalytic oxygen reduction reaction (ORR) features of two Co^II porphyrin(2.1.2.1) complexes bearing Ph or F₅ Ph groups at the two meso-positions of the macrocycle are examined. Single crystal X-ray analysis reveal a highly bent, nonplanar macrocyclic conformation of the complex resulting in clamp-shaped molecular structures. Cyclic voltammetry paired with UV/Vis spectroelectrochemistry in PhCN/0.1 M TBAP suggest that the first electron addition corresponds to a macrocyclic-centered reduction while spectral changes observed during the first oxidation are consistent with a metal-centered Co^II /Co^III process. The activity of the clamp-shaped complexes towards heterogeneous ORR in 0.1 M KOH show selectivity towards the 4e^- ORR pathway giving H₂ O. DFT first-principle calculations on the porphyrin catalyst indicates a lower overpotential for 4e^- ORR as compared to the 2e^- pathway, consistent with experimental data.