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  • 1965-1969  (5)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 132 (1965), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 90 (1968), S. 5307-5309 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 218 (1968), S. 574-575 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The importance of nutrition in host-parasite relationships has been reported in many studies4.7. Apple varieties have been rendered resistant to Venturia inaequalis by the injection of phenylalanine7. Tryptophan increased the indole acetic acid and so is involved m the formation of galls by ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 10 (1966), S. 1659-1672 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    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: Solubility and spectroscopic evidence are presented to support the formation of A-B block copolymers between monomers undergoing anionic polymerization (A units) and monomeric formaldehyde (B units). Comonomers included in the study were styrene, methyl and n-butyl methacrylate, acrylonitrile, isoprene, and N, N-di-n-butylacrylamide. Similar evidence is presented on the formation of B-A-B copolymers between styrene and α-methylstyrene and formaldehyde; an A-(B-C) random copolymer of styrene, formaldehyde, and phenyl isocyanate (C) was also prepared. Experimental details for the preparation of high-purity, monomeric formaldehyde suitable for such work is described in some detail. It should be emphasized that this study was directed primarily toward showing the feasibility of preparing formaldehyde block copolymers; therefore, further work is needed to establish the quantitative nature of these reactions.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 2001-2012 
    ISSN: 0449-296X
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Emulsion polymerization of methacrolein produces a polyacetal which can be converted through the action of sodium hydroxide to an alternating copolymer of methallyl alcohol and sodium methacrylate. Support for the alternating structure was gained primarily through a study of the polylactone formed through subsequent acidification of the sodium salt. Thus, the poly(methallyl alcohol-sodium methacrylate) copolymer was acidified under selected conditions to give a soluble polylactone containing 14.2 mole-% of residual acid and hydroxyl groups. This number agrees quite closely with the value of 13.5 mole-% which one would predict from the random cyclization of a true alternating copolymer. Cyclization of a random copolymer of poly(methallyl alcohol-sodium methacrylate) in a random fashion would have resulted in a value of about 36.8 mole-%. The results also support both the 1,2 vinyl polymerization of methacrolein and a nonrandom attack of the polymethacrolein by base. In a completely separate set of experiments, the value of r1 and r2 for the copolymerization of styrene (M1) and methacrolein (M2) were determined to be 0.22 ± 0.02 and 0.88 ± 0.02, respectively.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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