Abstract

The tridentate ligand N-(2-((2,6-diisopropylphenylimino)methyl)phenyl)quinolin-8-amine (HL) was prepared. Treatment of HL with 1 equiv of Ln(CH2SiMe3)3(THF)2 afforded the corresponding rare-earth metal bis(alkyl) complexes LLn(CH2SiMe3)2(THF)n (Ln = Sc, n = 0 (1); Y, n = 1 (2); Lu, n = 0 (3)) in high yields. Variable-temperature 1H NMR spectral analysis showed that these complexes were fluxional at room temperature. Complexes 1 and 3 were THF-free, where the metal center adopted a square-pyramidal geometry, while in 2 the metal center generated a distorted octahedral geometry owing to the coordination of a THF molecule. All these complexes catalyzed the ring-opening polymerization of ε-caprolactone with high activities in living fashion, among which the Lu complex was proved to be more active than its Sc and Y analogues.

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