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Spontaneous copolymerization of 4-methylene-1,3-dioxolanes with maleic anhydride

✍ Scribed by Fukuda, Hiroyuki ;Hirota, Masahiro ;Nakashima, Yoshihiro


Publisher
John Wiley and Sons
Year
1982
Weight
411 KB
Volume
20
Category
Article
ISSN
0360-6376

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✦ Synopsis


Abstract

The copolymerization of methylenedioxolanes, such as 4‐methylene‐1,3‐dioxolane (I) and 2,2‐dimethyl‐4‐methylene‐1,3‐dioxolane (II), with maleic anhydride (Manh) gives rise spontaneously to the alternating copolymers by the participation of charge‐transfer (CT) complexes. The formation of CT complexes I‐Manh and II‐Manh was ascertained by UV and NMR spectroscopies. The equilibrium constants (K) could not be determined but were assumed to be small (K ≪ 1). For comparison with these systems an investigation of I‐dimethyl maleate (DMM) and II‐DMM systems was carried out to estimate K values 0.115 and 0.157 L/mol, respectively. To clarify the copolymerization mechanism I‐Manh‐acryronitrile was terpolymerized. Consequently it was concluded that the spontaneous copolymerization of I‐Manh and II‐Manh systems is effected by the CT complex monomer mechanism.


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