Rutheniumethynyl-Triarylamine Organic-Inorganic Mixed-Valence Systems: Regulating Ru-N Electronic Coupling by Different Aryl Bridge Cores.

Abstract

Four rutheniumethynyl-triarylamine complexes 1-4 with different aryl bridge cores were prepared. The solid structures of complexes 2-4 were fully confirmed by X-ray single-crystal diffraction analysis. Two consecutive one-electron oxidation processes of complexes 1-4 were attributed to the ruthenium and nitrogen centers, as revealed by cyclic voltammetry and square-wave voltammogram. Results also showed decreasing potential difference ΔE of complexes 1, 3, and 4, with the largest value for 2. Upon chemical oxidation of complexes 1-4 by 1.0 eq oxidation reagents FcPF6 or AgSbF6 , the mixed-valence complexes, except for 2+ , show characteristic broad NIR absorptions in the UV-vis-NIR spectroscopic experiments. NIR multiple absorptions were assigned to NAr2 →RuCp*(dppe) intervalence charge transfer (IVCT) and metal-to-ligand charge transfer transitions by TDDFT calculations. Coupling parameter (Hab ) from Hush theory revealed that increasing electronic communication in 1+ , 3+ , and 4+ . Electron density distribution of the HOMO for neutral molecules (1, 3, and 4) and spin density distribution of the corresponding single-oxidized states (1+ , 3+ , and 4+ ) increases progressively on the bridge as the size of the aromatic system increases, proving incremental contributions from bridge cores during oxidation.