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Investigation of Silyl-Amide Complexes as Catalysts for the Ring-Opening Polymerization of L-Lactide
Corresponding Author(s) : Chanwoo Lee
Asian Journal of Chemistry,
Vol. 26 No. 13 (2014): Vol 26 Issue 13
Abstract
A series of silyl-amide complexes (= M{N(SiMe3)2}2) were examined as the catalysts for the ring-opening polymerization of L-lactide. The poly(L-lactic acid) (PLLA) synthesized with the Zn complex showed a Mn near the theoretical value with narrow dispersity. The Zn complex without 1-dodecanol added also gave a poly(L-lactic acid) with Mn near 10,000 Da, although its molecular weight distribution was wide. The poly(L-lactic acid) obtained with the Sn complex in the absence of 1-dodecanol had a Mn higher than 40,000 Da, suggesting that the Sn catalyst involved in the insertion reaction with lactide should have higher activity for the polymerization. This steric space makes the coordination of L-lactide easier and causes faster rate of conversion in the early stage of the polymerization despite its small polarization.
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F.E. Kohn, J.W.A. Van Den Berg, G. Van De Ridder and J. Feijen, J. Appl. Polym. Sci., 29, 4265 (1984); doi:10.1002/app.1984.070291255.
J.W. Leenslag and A.J. Pennings, Polymer, 28, 1695 (1987); doi:10.1016/0032-3861(87)90012-7.
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M. Ajioka, E. Enomoto, K. Suzuki and A. Yamaguchi, Bull. Chem. Soc. Jpn., 68, 2125 (1995); doi:10.1246/bcsj.68.2125.
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J. Cai, K.J. Zhu and S.L. Yang, Polymer, 39, 4409 (1998); doi:10.1016/S0032-3861(97)10346-9.
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H. Ma and J. Okuda, Macromolecules, 38, 2665 (2005); doi:10.1021/ma048284l.
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C.W. Lee, S. Kuno and Y. Kimura, Macromolecular Res., 21, 385 (2013); doi:10.1007/s13233-013-1033-6.
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