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  • 1960-1964  (3)
  • 1960  (3)
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  • 1960-1964  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 509-516 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Chain transfer constants of the end groups (CE) and of the middle portions (CM) of the polymer chain of polyethylene glycol and its dodecyl ether were determined at 60°C. in vinyl acetate polymerization. In the case of polyethylene glycol, CE and CM represent the chain transfer constants of (HO—C2H4—) and that of (—CH2CH2O—) which were estimated as 0.004 and 0.0017 respectively, and were compared with the chain transfer constants of propanol and ethanol. The chain transfer constant of the dodecyl radical in polyethylene glycol dodecyl ether is estimated as 0.001, which is in fairly good agreement with that obtained theoretically from the chain transfer constant of the methylene group in acetic esters, but not from that in alcohols. This situation may be attributed to the inhibition of resonance energy transfer by the etherlike oxygen atom.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 46 (1960), S. 539-541 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 42 (1960), S. 535-544 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The present investigation is concerned with the relationship between P, the reactivity of a radical, and Q that of a monomer in the propagation reaction. At first, P values are calculated from the accumulated data of the rate constants of the propagation reaction. From these results, the relation is shown to be represented by the following equation: \documentclass{article}\pagestyle{empty}\begin{document}$ \log {\rm }P = kQ + a(k 〈 0) $\end{document} where k and a are constants. The P values in the termination reaction (Pt) are also calculated, and the relation between these values and Q values are examined. The results show that the similar relation found in the propagation reaction holds in this step too. By applying the method of Evans and co-workers, a sufficient explanation for this equation is not obtained, but the analogous equation can be derived. The present authors suggest that the inverse proportion between log P and Q appears to be based on the following different principles: (1) the inverse proportion between the magnitude of localization energy of the radical and that of monomer, and (2) the linear free energy relationship found in organic chemistry.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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