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Issue 4, 2020
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Isoselective ring-opening polymerization and asymmetric kinetic resolution polymerization of rac-lactide catalyzed by bifunctional iminophosphorane–thiourea/urea catalysts

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Abstract

A series of iminophosphorane–thiourea/urea bifunctional catalysts was synthesized and utilized for the isoselective ring-opening polymerization of rac-lactide. The ROPs were promoted efficiently, affording the polylactides with controlled molecular weight, narrow molecular weight distribution and well-defined end groups without undesired side reactions. The experiment data revealed that ROPs of rac-LA are a “controlled/living” process. The highest stereoselectivity (Pm) was up to 0.80 using rac-IPU-1 under mild reaction conditions. The mechanistic study indicated that stereoselective ROPs of rac-LA were mainly controlled by a chain-end control mechanism when using rac/(R,R)-IPTU-1/IPU-1 as catalysts. Additionally, the ee values of −11% at 0 °C and −17% at −40 °C were achieved at about 50% conversion using (S)-IPU-2 as a chiral catalyst. The selectivity factor (s = kL/kD) of 1.6 indicated that a clear kinetic resolution occurred and the enantiomorphic site control mechanism was involved.

Graphical abstract: Isoselective ring-opening polymerization and asymmetric kinetic resolution polymerization of rac-lactide catalyzed by bifunctional iminophosphorane–thiourea/urea catalysts

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Supplementary files

Article information


Submitted
09 Oct 2019
Accepted
15 Dec 2019
First published
16 Dec 2019

New J. Chem., 2020,44, 1648-1655
Article type
Paper

Isoselective ring-opening polymerization and asymmetric kinetic resolution polymerization of rac-lactide catalyzed by bifunctional iminophosphorane–thiourea/urea catalysts

C. Lv, L. Zhou, R. Yuan, Q. Mahmood, G. Xu and Q. Wang, New J. Chem., 2020, 44, 1648 DOI: 10.1039/C9NJ05074D

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