## 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
Group-transfer alternating copolymerization of 2-phenyl-1,3,2-dioxaphosphorinane with trimethylsilyl 2-(acryloyloxy)ethanesulfonate
✍ Scribed by Shiro Kobayashi; Jun-ichi Kadokawa
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 401 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
This paper describes a new class of reaction, group‐transfer alternating copolymerization (GTAC), between 2‐phenyl‐1,3,2‐dioxaphosphorinane (1) and trimethylsilyl 2‐(acryloyloxy)ethanesulfonate (2). The copolymerization took place without any added catalyst and proceeded via quantitative trimethylsilyl group‐transfer process to give a 1:1 alternating copolymer 3a having a ketene silyl acetal group in the main chain. Results of spectroscopy as well as alkaline hydrolysis and bromination of the copolymer confirmed the structure.
📜 SIMILAR VOLUMES
## Abstract Ring‐opening polymerization of 2‐phenyl‐1,3,2‐dioxaphosphorinane (a six‐membered cyclic phosphonite, 4) has been initiated with a new catalyst system of a halobenzene and NiBr~2~. The polymerization proceeded in a living nature to produce poly(phosphinate) consisting exclusively of a “n
## Abstract Copolymerization of ethylene chlorophosphonite (ECP) with 2‐phenyl‐1,3‐dioxolane (PhD) and the flame‐retardant effect of the copolymer on polyester fabric were investigated. (1) Copolymerization occurred without added catalyzer. The number‐average molecular weight ranged from 600 to 100