Coordination structure conversion of protonated bisporphyrinato terbium(iii) double-decker complexes and creation of a Kondo assembly by electron injection on the Au(111) surface.

The first step towards the synthesis of single-molecule magnet (SMM)-based spintronics devices is the organization and manipulation of magnetic molecules on surfaces. Our previous studies on bulk crystals demonstrated that protonated porphyrinato double-decker complexes [Tb(Hoep)(oep)] (oep = 2,3,7,8,12,13,17,18-octaethylporphyrinato) are not SMMs; however, once a hydrogen is removed to produce their neutral radical forms, [Tb(oep)], they convert to SMMs. These intriguing properties encouraged us to examine the electronic/spin properties of these complexes and their chemical conversion ability after their transfer onto a metal substrate, similar to the environment required for the practical application of SMMs.