Random copolymerization of trimethylene carbonate (TMC) with e-caprolactone (CL) catalyzed by rare earth chloride-epoxide or rare earth isopropoxide has been investigated for the first time. It was found that in the presence of epoxide, rare earth chlorides have high activities for the copolymerizat
Copolymerizations of carbon dioxide and epoxides in the presence of rare earth coordinate catalyst
β Scribed by Jin-Tang Guo; Xin-Ying Wang; Yong-Shen Xu; Jing-Wu Sun
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 73 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Abstract
Carbon dioxide (CO~2~) as a direct material was copolymerized with epoxides to synthesize new aliphatic polycarbonates, and the copolymerization was catalyzed by the coordinate catalyst composed of rare earth yttrium phosphonate and triisobutylaluminum [Y(P~204~)~3~βA1(iβBu)~3~]. The epoxides used in this research included epichlorohydrin (ECH) and some new glycidol ether (GE) monomers prepared by the reaction of ECH and phenol or alcohol, such as Ξ±βallyl glycidol ether, Ξ²βchloroethyl glycidol ether, benzene glycidol ether, mβtolyl glycidol ether, and benzyl glycidol ether. The copolymers were characterized by infrared (IR), ^1^H nuclear magnetic resonance (βNMR), and dynamic mechanical analysis. The results show that Y(P~204~)~3~βA1(iβBu)~3~ had better catalytic activity in the copolymerization of CO~2~ with epoxide, and the copolymerization rate of aryl GE was distinctly higher than that of aliphatic GE. Dynamic mechanical analysis indicated the glass transition temperature T~g~ of the copolymers GEβCO~2~ were lower than that of ECHβCO~2~. Β© 2003 Wiley Periodicals, Inc. J Appl Polym Sci 87: 2356β2359, 2003
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