## Abstract The stereochemistry of alternating copolymerization of carbon dioxide with __S__‐(–)‐3‐phenyl‐1,2‐epoxypropane (**5**) using a diethylzinc/water system as catalyst was investigated. The optically active copolymer, poly[(oxycarbonyloxy)‐1‐benzylethylene] (**6**), was hydrolyzed and the e
Copolymerization of 3,3,3-trifluoro-1,2-epoxypropane with N-phenylmaleimide using organozinc initiators
✍ Scribed by Yoji Ikeda; Yasuhiko Yoshida; Kenji Ishihara; Hiroshi Hamana; Tadashi Narita; Tokio Hagiwara
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 367 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
Novel copolymers consisting of 3,3,3‐trifluoro‐1,2‐epoxypropane (TFEP) and N‐phenylmaleimide (PMI) units were prepared by the copolymerization of TFEP with PMI initiated with an organozinc compound. Using [Zn(OCH~3~)~2~ · (C~2~H~5~ZnOCH~3~)~4~] as an initiator, the copolymer chains consisted mainly of TFEP‐TFEP sequences. The TFEP‐PMI sequence content in the copolymer chains was small. On the other hand, using (C~2~H~5~ZnOCH~3~)~4~ as an initiator, only low molecular weight copolymers were formed. Those copolymers were suggested to have block structure, poly(TFEP)‐block‐poly(PMI), by the ^19^F NMR analysis. The copolymers showed higher thermostability than poly‐(TFEP).
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