Synthesis, characterization and functionalization of titanium κ amidinato complexes from carbodiimides.

A series of titanium amidinato complexes were synthesized by stoichiometric insertion reactions of carbodiimides into bis(π-η:σ-η-pentafulvene)titanium complexes. NMR studies and single-crystal X-ray diffraction showed κ coordination of the former carbodiimides to the metal center. DFT calculations were performed, confirming the clear preference for a single nitrogen atom coordinating to the metal center with a high energy transition state for the formation of a chelating heteroallyl ligand.