Effect of porphyrin ligands on the catalytic CH4 oxidation activity of monocationic μ-nitrido-bridged iron porphyrinoid dimers by using H2O2 as an oxidant

Abstract

The μ-nitrido-bridged iron phthalocyanine homodimer is a potent molecule-based CH₄ oxidation catalyst that can effectively oxidize chemically stable CH₄ under mild reaction conditions in an acidic aqueous solution including an oxidant such as H₂O₂. The reactive intermediate is a high-valent iron-oxo species generated upon reaction with H₂O₂. However, a detailed comparison of the CH₄ oxidation activity of the μ-nitrido-bridged iron phthalocyanine dimer with those of μ-nitrido-bridged iron porphyrinoid dimers containing one or two porphyrin ring(s) has not been yet reported, although porphyrins are the most important class of porphyrinoids. Herein, we compare the catalytic CH₄ and CH₃CH₃ oxidation activities of a monocationic μ-nitrido-bridged iron porphyrin homodimer and a monocationic μ-nitrido-bridged heterodimer of an iron porphyrin and an iron phthalocyanine with those of a monocationic μ-nitrido-bridged iron phthalocyanine homodimer in an acidic aqueous solution containing H₂O₂ as an oxidant. It was demonstrated that the CH₄ oxidation activities of monocationic μ-nitrido-bridged iron porphyrinoid dimers containing porphyrin ring(s) were much lower than that of a monocationic μ-nitrido-bridged iron phthalocyanine homodimer. These findings suggested that the difference in the electronic structure of the porphyrinoid rings of monocationic μ-nitrido-bridged iron porphyrinoid dimers strongly affected their catalytic light alkane oxidation activities.