A series of bimetallic Salen aluminum (III) complexes with different steric substituents were synthesized.
These complexes were used as catalysts to produce polylactide in the ring-opening polymerization of racemic
lactide. A kinetic research of polymerization demonstrated that the steric substituents on the phenolate ring of
the complexes had remarkable infl uence on the stereoselectivity and the polymerization activity. The highest
stereoselectivity was obtained with bulky substituent on the ortho position of the salicylidene moieties. Kinetic
studies using all these complexes indicated that the polymerizations were fi rst-ordered with respect to lactide
monomers. All these complexes gave highly isotactic polylactides with controlled molecular weight and
narrow molecular weight distributions.
Cite This Article
APA Style
Sun, Z., Duan, R., Zhang, H., Pang, X., Wang, X. et al. (2015). Highly stereoselective polymerization of racemic lactide by bimetallic schiff base complexes. Journal of Renewable Materials, 3(2), 82-90. https://doi.org/10.7569/JRM.2014.634133
Vancouver Style
Sun Z, Duan R, Zhang H, Pang X, Wang X, Chen X. Highly stereoselective polymerization of racemic lactide by bimetallic schiff base complexes. J Renew Mater. 2015;3(2):82-90 https://doi.org/10.7569/JRM.2014.634133
IEEE Style
Z. Sun, R. Duan, H. Zhang, X. Pang, X. Wang, and X. Chen "Highly Stereoselective Polymerization of Racemic Lactide by Bimetallic Schiff Base Complexes," J. Renew. Mater., vol. 3, no. 2, pp. 82-90. 2015. https://doi.org/10.7569/JRM.2014.634133