Conceptual

Atomic-Scale d-pi-d Spin Coupling in Metal-Organic Coordination Structures

Direct scanning-tunneling-microscopy observation of exchange coupling between iron d electrons and organic-radical pi systems in a well-defined two-Fe, four-radical coordination unit. Shows that simultaneous antiferromagnetic coupling of each metal to the radical ligands aligns the metal-dimer spins into a ferrimagnetic state, explained by density functional and valence bond theory.