Polymerization of Diallyl Alkyl Isocyanurates
Autor: | Tsukasa Matsumoto, Mikio Hirabayashi, Tsuneo Nakanishi, Akinori Kameyama, Katsuyuki Watanabe, Akira Matsumoto, Hiroyuki Aota |
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Rok vydání: | 1998 |
Předmět: |
Steric effects
chemistry.chemical_classification Gel point Polymers and Plastics Bulk polymerization Kinetics Radical polymerization technology industry and agriculture macromolecular substances General Chemistry Chain length chemistry Polymerization Polymer chemistry Materials Chemistry Ceramics and Composites Alkyl |
Zdroj: | Journal of Macromolecular Science, Part A. 35:1889-1893 |
ISSN: | 1520-5738 1060-1325 |
DOI: | 10.1080/10601329808000559 |
Popis: | Polymerizations of several diallyl alkyl isocyanurates were investigated to explore in more detail the steric effect observed in the polymerization of triallyl isocyanurate [3, 5], as compared to its isomer triallyl cyanurate, by changing alkyl groups from methyl, propyl, hexyl, and octyl up to lauryl. The rate of polymerization, the gel point, the cyclization constant, and the primary chain length were evaluated. For example, the primary chain length increased with an increase in the bulkiness of the alkyl group as expected, although in the polymerization of diallyl lauryl isocyanurate it decreased as a reflection of reduced rate of propagation due to the enhanced steric effect arising from a very bulky lauryl group. |
Databáze: | OpenAIRE |
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