Highly Electron‐Rich β‐Diketiminato Systems: Synthesis and Coordination Chemistry of Amino‐Functionalized “<i>N</i>‐nacnac” Ligands

Abstract

The synthesis of a class of electron-rich amino-functionalized β-diketiminato (N-nacnac) ligands is reported, with two synthetic methodologies having been developed for systems bearing backbone NMe₂ or NEt₂ groups and a range of N-bound aryl substituents. In contrast to their (Nacnac)H counterparts, the structures of the protio-ligands feature the bis(imine) tautomer and a backbone CH₂ group. Direct metalation with lithium, magnesium, or aluminium alkyls allows access to the respective metal complexes through deprotonation of the methylene function; in each case X-ray structures are consistent with a delocalized imino-amide ligand description. Transmetalation using lithium N-nacnac complexes is then exploited to access p- and f-block metal complexes, which allow for like-for-like benchmarking of the N-nacnac ligand family against their more familiar Nacnac counterparts. In the case of Sn^II , the degree of electronic perturbation effected by introduction of the backbone NR₂ groups appears to be constrained by the inability of the amino group to achieve effective conjugation with the N₂ C₃ heterocycle. More obvious divergence from established structural norms is observed for complexes of the harder Yb^II ion, with azaallyl/imino and even azaallyl/NMe₂ coordination modes being demonstrated by X-ray crystallography.