Zirconium and hafnium complexes bearing pyrrolidine derived salalen-type {ONNO} ligands and their application for ring-opening polymerization of lactides.

Dalton Trans

Key Laboratory of Nonferrous Metals Chemistry and Resources Utilization of Gansu Province, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, Gansu, P. R. China.

Published: August 2017

The reactions of pyrrolidine derived salalen-type {ONNO} ligands (S)-L-H with 1 equiv. M(OPr)(HOPr) (M = Zr or Hf) in diethyl ether yielded complexes [LM(OPr)] (L = L, M = Zr (1); L = L, M = Zr (2), Hf (3); L = L, M = Zr (4), Hf (5)). All of these complexes were well characterized by NMR spectroscopy, elemental analyses and single-crystal X-ray analysis in the case of complexes 1 and 3-5. X-ray structural determination revealed that these complexes were analogous mononuclear species and had a similar structure in which the metal centers were six-coordinated to two oxygen atoms and two nitrogen atoms of one ligand and two oxygen atoms of two isopropoxy groups. All of these complexes efficiently initialized the ring-opening polymerization of lactides to afford polymers with controlled molecular weight and narrow polydispersity. Furthermore, the ring-opening polymerization of rac-lactide catalyzed by complexes 1-5 afforded isotactic-enriched polymers in solution (P = 0.74-0.80) and under melt conditions (P = 0.63-0.72).

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http://dx.doi.org/10.1039/c7dt02113eDOI Listing

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