Toward understanding macrocycle specificity of iron on the dioxygen-binding ability: a theoretical study

Abstract

In an effort to examine the interaction between dioxygen and iron-macrocyclic complexes, and to understand how this interaction was affected by those different macrocyclic ligands, dioxygen binding with iron-porphyrin, iron-phthalocyanine, iron-dibenzotetraaza[14]annulene, and iron-salen complexes is investigated by means of quantum chemical calculations utilizing Density Functional Theory (DFT). Based on the analysis of factors influencing the corresponding dioxygen binding process, it showed that different macrocyclic ligands possess different O–O bond distances, and different electronic configurations for the bound O₂ and non-aromatic macrocyclic ligands favor dioxygen activation. Furthermore, the smaller the energy gap between the HOMO of iron–macrocyclic complexes and the LUMO of dioxygen, the more active the bound O₂ becomes, with a longer O–O bond distance and a shorter Fe–O bond length.