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  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 3 (1963), S. 50-56 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Monomers for which the necessary information was obtained for comparison included the following: styrene, α-methylstyrene, cis and trans-propenylbenzene, allylbenzene, m-methylstyrene, p-methylstyrene, o-, m-, and p-chlorostyrene, 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, and 3,5-dichlorostyrene, p-ethylstyrene, and p-tert-butylstyrene. In both free radical and ionic copolymerizations involving similar monomers, plots of the logarithms of the relative reactivities of several substituted styrenes toward the styrene and methyl methacrylate radicals versus the differences existing between the exaltations of substituted styrenes and the exaltation of styrene were strikingly similar to those in which Hammett's sigma values for the styrene substituents were plotted against the relative reactivities of the substituted styrenes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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