A novel synthetic route to poly(β-ketone)s via poly(alkoxyethyne)s
✍ Scribed by Shin-ichiro Shoda; Akio Komenoi; Tomochika Fujioka; Yasunori Okumura; Shiro Kobayashi
- Book ID
- 102482743
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 360 KB
- Volume
- 197
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Isopropoxyethyne (1a) and tert‐butoxyethyne (1b) were polymerized using group 5 and 6 transition metal catalysts to give poly(isopropoxyethyne) (2a) and poly(tert‐butoxyethyne) (2b), respectively. The weight‐average molecular weight (M̄~w~) of the resulting poly(alkoxyethyne)s was up to 1.0 × 10^4^. Among the transition metal catalysts, a tungsten alkoxide or a molybdenum alkoxide having low Lewis acidity were found to effectively promote the polymerization without causing side reactions. Poly(tert‐butoxyethyne) was successfully converted to poly(β‐ketone) 3 by acid hydrolysis of the tert‐butyl vinyl moiety.
📜 SIMILAR VOLUMES