Copolymerizations of 4-methylene-2-styryl-1,3-dioxolane (1) and 4-methylene-%methyl-Z-styryl-1,3-dioxolane (2) with electron-deficient monomers, such as maleic anhydride (MA) and acrylonitrile (AN) were investigated. Only homopolymer of 1 was obtained from the copolymerization of 1 with MA in the pr
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.
📜 SIMILAR VOLUMES
Photoinitiated polymerization of 4-methylene-2-phenyl-1,3-dioxolane ( 1) was carried out using either tris(4-methylphenyl)sulfonium hexafluoroantimonate or 4-decyloxyphenyl phenyliodonium hexafluoroantimonate as initiators. 1 H-NMR analyses confirmed exclusive ring-opening while DSC and SEC were use