Rare Earth Metal Complexes Supported by a Tripodal Tris(amido) Ligand System Featuring an Arene Anchor

Abstract

A new tripodal tris(amido) ligand system featuring an arene anchor was developed and applied to the coordination chemistry of rare earth metals. Two tris(amido) ligands with a 1,3,5-triphenylbenzene backbone were prepared in two steps from commercially available reagents on a gram scale. Salt metathesis and alkane elimination reactions were exploited to prepare mononuclear rare earth metal complexes in moderate to good yields. For salt metathesis reactions, while metal tribromides yielded neutral metal tris(amido) complexes, metal trichlorides led to the formation of ate complexes with an additional chloride bound to the metal center. The new compounds were characterized by X-ray crystallography, elemental analysis, and 1H and 13C nuclear magnetic resonance spectroscopy. The rare earth metal complexes exhibit a trigonal planar coordination geometry for the [MN3] fragment in the solid state rather than a trigonal pyramidal geometry, commonly observed for rare earth metal tris(amido) complexes such as M[N(SiMe3)2]3. Moreover, the arene anchor of the tripodal ligands is engaged in a nonnegligible interaction with the rare earth metal ions. Density functional theory calculations were performed to gain insight into the bonding interactions between the tripodal ligands and the rare earth metal ions. While LUMOs of these rare earth metal complexes are mainly π* orbitals of the arene with a minor component of metal-based orbitals, HOMO-15 and HOMO-16 of a lanthanum complex show that the arene anchor serves as a π donor to the trivalent lanthanum ion.