Microscopic origins of the ferromagnetic exchange coupling in oxoverdazyl-based Cu(II) complex

Abstract

The exchange channels governing the experimentally reported coupling constant (Jexpt=6 cm-1) value in the verdazyl-ligand based Cu(II) complex [Cu(hfac)2(imvdz)] are inspected using wave function-based difference dedicated configuration interaction calculations. The interaction between the two spin 1/2 holders is summed up in a unique coupling constant J. Nevertheless, by gradually increasing the level of calculation, different mechanisms of interaction are turned on step by step. In the present system, the calculated exchange interaction then appears alternatively ferromagnetic/antiferromagnetic/ferromagnetic. Our analysis demonstrates the tremendously importance of some specific exchange mechanisms. It is actually shown that both parts of the imvdz ligand simultaneously influence the ferromagnetic behavior which ultimately reaches Jcalc=6.3 cm -1, in very good agreement with the experimental value. In accordance with the alternation of J, it is shown that the nature of the magnetic behavior results from competing channels. First, an antiferromagnetic contribution can be essentially attributed to single excitations involving the π network localized on the verdazyl part. In contrast, the σ ligand-to-metal charge transfer (LMCT) involving the imidazole moiety affords a ferromagnetic contribution. The distinct nature σ/π of the mechanisms is responsible for the net ferromagnetic behavior. The intuitively innocent part of the verdazyl-based ligands is deeply reconsidered and opens new routes into the rational design of magnetic objects. © 2010 American Institute of Physics.