KOBUNSHI RONBUNSHU
Online ISSN : 1881-5685
Print ISSN : 0386-2186
ISSN-L : 0386-2186
Pyridine-Catalyzed Polymerization of α-Cyanovinyl Acetate
Seizo MASUDATadatoshi OTA
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1979 Volume 36 Issue 5 Pages 343-346

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Abstract

α-Cyanovinyl acetate (α-CN·VAc) is polymerized anionically at 70°C in the presence of pyridine, a weak base, although the presence of strong base such as butyllithium leads to decomposition of the monomer. The anionic polymerization accompanies radical polymerization at a relatively high temperature. Pyridine in concentration up to 0.12 mol/l works inhibitory for the radical polymerization of α-CN·VAc, while it serves efficiently as anionic catalyst in the presence of p-benzoquinone. The rate of the anionic polymerization is directly proportional to the concentration of pyridine. In the anionic bulk-copolymerization of α-CN·VAc (M1) and styrene (M2), pyridine-benzoquinone catalyst gives r1=10.0 and r2=0.01.

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© The Society of Polymer Science, Japan
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