Kinetics of ring-opening radical polymerization of vinyloxiranes
β Scribed by Osamu Ito; Tatsushi Ishizuka; Masashi Iino; Minoru Matsuda; Takeshi Endo; Tsutomu Yokozawa
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 375 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0538-8066
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β¦ Synopsis
Ring-opening radical polymerization has been followed by the flash photolysis method. As a n initiator radical, the arylthiyl radical (ArS') was used; the addition reaction rate constants of ArS' to vinyl monomer containing epoxy-ring such as vinyloxiranes (CH2 = C H C m H 2 ) have been determined at first. The rate constant of ring opening reaction of the adduct radical (ArSCH2C'HCmHZ) changing to ArSCH2CH =CRQCH2' were determined in the form of the relative values, which were converted to the absolute values. The ring-opening reaction rate constants were ca. lo6 s-', which indicates that the ring-opening rates are faster than usual radical propagation rates. The rate constants for vinyl monomer with &member ring (1,4-epoxy-1,4-dihydronaphthalene) were similarly evaluated.
π SIMILAR VOLUMES
Radical emulsion polymerizations of vinylcyclopropanes, 1,1-bis(ethoxycarbonyl)-2-vinylcyclopropane (ECVCP) and 1,1-dichloro-2-vinylcyclopropane (CVCP) were examined. ECVCP underwent soap-free and soap-in emulsion polymerizations satisfactorily to afford the ring-opened polymer in good yields. Polym
Title from title screen (viewed Aug. 13, 2004).Made available through Wiley InterScience online books.Previous ed.: 1991.Includes bibliographical references and index.Electronic reproduction.[New York] :J. Wiley and Sons,[200u]Mode of access: World Wide Web.
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