## Abstract 2‐Methylene‐1,3‐dioxepane 6 polymerized with a quantitative ring opening to form poly‐ϵ‐caprolactone via a free radical mechanism. On the other hand, 2‐methylene‐1,3‐dioxolane (ethylene ketene acetal) 4 and 2‐methylene‐1,3‐dioxane 5, under the same conditions, generated polymers with mi
Photoinitiated ring-opening polymerization of 2-methylene-1,3-dioxepane
✍ Scribed by Takeshi Endo; Makoto Okawara; W. J. Bailey; Kazufumi Azuma; Kazuo Nate; Hitoshi Yokono
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1983
- Tongue
- English
- Weight
- 200 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0887-6258
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📜 SIMILAR VOLUMES
BF 3 rOEt 2 -initiated polymerizations of 2-methylene-1,3-dioxepane gave polymers composed of both ring-retained and ring-opened structures. The ring-opening content increased with an increase in polymerization temperature. Poly(4,7-dimethyl-2-methylene-1,3-dioxepane) propagated slower during BF 3 r
The stable cyclic ketene acetal, 2-metbylene-1,3-dioxepane, 7, has been polymerized cat ionically in pentane, CHzClj and THF at 25°C to form a polymer which is composed of both ring-opened (40-50% ) and ring-retained (50-60%) structures. Init iatiorr was catalyzed by using H2S0, -supported on activa