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  • 1
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-Methylacrylamide (NMAAm) was polymerized quantitatively by using di-tert-butyl peroxide as photosensitizer to be, for the most part, incorporated in living poly(NMAAm) radical. The living polymer radical reacted effectively with acrylate monomers to yield block copolymer. Longer alkyl chain of the acrylate monomer caused a decrease in the conversion of the second monomer. Methacrylate monomers, such as methyl methacrylate and cyclohexyl methacrylate, showed relatively low reactivities in comparison with acrylates. Styrene exhibited a much lower conversion. The resulting block copolymers showed different thermochromic behaviors in methyl benzoate from that of poly(NMAAm). This is explained on the basis of the difference between refractive indexes of the block copolymers and poly(NMAAm).
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 943-952 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: N-methylacrylamide (NMAAm) and N-methylmethacrylamide (NMMAm) were polymerized to give polymer microspheres containing living propagating radicals. The microsphere polymer radicals were allowed to react with some binary mixtures of vinyl monomers including alternating copolymerization combinations. The reaction processes were investigated by ESR spectroscopy. In the poly(NMMAm) radical/methyl methacrylate (MMA)/styrene (St) system, the propagating radical from MMA was mainly observed at the higher MMA concentration, while polySt radical prevailed at the lower MMA concentration. In the poly(NMMAm) radical/α-methylstyrene (α-MeSt)/diethyl fumarate system, the α-MeSt radical was exclusively observed, while the maleic anhydride (MAn) radical was predominantly observed in the α-MeSt/MAn system. In the MAn/diphenylethylene system, the propagating radicals from both monomers were observed at comparable concentrations. The poly(NMAAm) microsphere radical behaved differently in the reaction with the MMA/St mixture. The poly(NMAAm) microsphere was found to incorporate preferentially St, leading to formation of the St radical. The St preference was enhanced in the St/cyclohexyl methacrylate (CHMA) system. These results were in agreement with those of block copolymerization via the reaction of poly(NMAAm) radical with the MMA/St or CHMA/St mixture, where the compositions of the resulting polymers were analyzed by pyrolysis gas chromatography.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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