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  • 1960-1964  (2)
  • Chemistry  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 3 (1960), S. 310-315 
    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: The preparation of condensation products of poly(4-vinyl-acetophenone) with various substituted benzaldehydes is described. As in the case of the products obtained by condensing the poly(4-vinylacetophenone) with benzaldehyde, these, too, show to varying degrees the property of becoming insoluble when exposed to light. This sensitivity to light is generally higher where the aldehyde used contains electrondonating substituent groups in the para-position. This, in turn, is also related to the ability of such products to absorb a larger proportion of the longer wavelength portion of the emitted light.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 43 (1960), S. 1915-1927 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The rates of racemisation, under constant conditions of pH and temperature, of two series of ketones with an asymmetric C-atom in α have been determined. As would be expected, substituents in the α position to the keto group influence the rate of racemisation, and it has been found possible to assess the relative electron donating or electron attracting effect of aliphatic, aliphatic-aromatic or aromatic substituents by measuring their influence on the rate of racemisation of a ketone containing the substituent considered.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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