## Abstract 1‐Propen‐1‐ylidene dicyanide was copolymerized in bulk with vinyl acetate and five substituted styrenes. The reactivity ratios of these copolymerizations were calculated by the Fineman‐Ross or the Kelen‐T¨︁udős method. The penultimate model describes satisfactorily the deviation from th
Polymérisation et copolymérisation d'acétoxy-2 alcadiènes-1,3 – l'acétate de (cyclopentène-1 yle)-1 vinyle et l'acétate de (méthyl-3 butadiène-1,3) yle- 2 – formation des polycétones correspondantes
✍ Scribed by Bonnans-Plaisance, Chantal ;Casals, Pierre-François ;Levesque, Guy
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1979
- Weight
- 489 KB
- Volume
- 180
- Category
- Article
- ISSN
- 0025-116X
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✦ Synopsis
Abstract
The polymerization of 1‐(1‐cyclopentenyl)vinyl acetate (1) and (3‐methyl‐1,3‐butadien‐2‐yl) acetate (7) under radical conditions, leading to 1,4‐polymers, and the copolymerization with vinyl monomers were studied. The reactivity ratios are compared with those previously described for some acetoxydienes. Polyketones and copolyketones were obtained by alkaline hydrolysis of the polymers of 1 and 7 and copolymers of 1 and 7 with styrene.
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