Dinuclear oxidative addition reactions using an isostructural series of Ni2, Co2, and Fe2 complexes

Abstract

A family of low-valent Ni₂, Co₂, and Fe₂ naphthyridine–diimine (NDI) complexes is presented. Ligand-based π* orbitals are sufficiently low-lying to fall within the metal 3d manifold, resulting in electronic structures that are highly delocalized across the conjugated [NDI]M₂ system. This feature confers stability to metal–metal interactions during two-electron redox reactions, as demonstrated in a prototypical oxidative addition of allyl chloride.