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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 1015-1024 
    ISSN: 0887-624X
    Keywords: ambifunctional monomers ; 1-propenyl ethers ; 1-butenyl ethers ; vinyl ethers ; cationic polymerization ; photopolymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of a novel series of ambifunctional monomers containing cationically polymerizable vinyl and 1-propenyl ether or 1-butenyl ether groups in the same molecule has been carried out. Studies of the onium salt-induced photopolymerizations of these monomers indicate that both functional groups are highly reactive and that they undergo extensive copolymerization. © 1996 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 34 (1996), S. 2051-2062 
    ISSN: 0887-624X
    Keywords: 1-propenyl ether monomers ; trimethylolpropane diallyl ether ; photoinitiated cationic polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of nine difunctional 1-propenyl ether monomers bearing ether, ester, carbonate, and urethane groups were prepared based on trimethylolpropane diallyl ether as the starting material. The monomers were fully characterized and then subjected to photoinitiated cationic polymerization using diaryliodonium salts as photoinitiators. The course of the polymerizations was followed using Fourier transform real-time infrared spectroscopy and the relative reactivities of the various monomers were determined. It could be shown that the differences in reactivity could be related mainly to the basicity of the functional group introduced into the molecule. © 1996 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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