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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of organic chemistry 30 (1965), S. 1229-1231 
    ISSN: 1520-6904
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    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 82 (1960), S. 6000-6005 
    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. : American Chemical Society
    Journal of the American Chemical Society 81 (1959), S. 1345-1348 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 86 (1964), S. 4791-4795 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 43 (1960), S. 445-452 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Monomer reactivity ratios have been determined for the copolymerization of methyl methacrylate (M1) and acrylonitrile (M2) catalyzed by alkyl derivatives of lithium, sodium, beryllium, magnesium, boron, aluminum, zinc, and cadmium. Lithium, sodium, beryllium, and magnesium alkyls gave reactivity ratios averaging r1 = 0.34, r2 = 6.7, while alkyls of boron, aluminum, zinc, and cadmium gave r1 = 1.24, r2 = 0.11. These values compare favorably with published reactivity ratios for anionic copolymerization (r1 = 0.25, r2 = 7.9) and free-radical copolymerization (r1 = 1.35, r2 = 0.18). Therefore, alkyl derivatives of groups Ia and IIa metals propagate by an anionic mechanism, while those of groups IIb and IIIa do so by a free-radical mechanism. Confirmatory experiments were run using styrene (M1)-acrylonitrile (M2) solutions. For groups Ia and IIa alkyls the reactivity ratios averaged, r1 = 0.20, r2 = 12.5; and for Groups IIb and IIIa r1 = 0.33, r2 = 0.03. The published values for free-radical catalysts are r1 = 0.41, r2 = 0.04. The formation of free radicals from the groups IIb and IIIa metal alkyls probably arises from oxidation of the metal alkyls by chance traces of oxygen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 56 (1962), S. 225-231 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Both the glass transition temperature and the melting point of poly(vinyl chloride have been found to increase as the temperature at which the ample is polymerized is decreased). The glass transition temperature changes from about 70°C. for polymer prepared at 125°C. to about 100°C. for polymer prepared at -80°C. It is believed the increase in percentage of syndiotactic structure which results from decreasing the polymerization temperature is responsible for the change in glass transition temperature. The effect of polymerization temperature on melting point is even more striking. The melting point changes from approximately 160 to above 300°C. on lowering the polymerization temperature from 125 to -80°C. X-ray diffraction studies show that polymers prepared at low temperature form crystals which have a substantial increase in perfection along the chain axis. It seems probable that this increase in crystalline perfection along the chain axis is responsible for the very marked increase in melting point.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 61 (1962), S. 243-252 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of oxygen on the rate of polymerization of methyl methacrylate catalyzed by triethylboron has been investigated at temperatures in the range 0-52°C. In the absence of oxygen polymerization does not occur, but formation of polymer begins immediately on admission of oxygen. Polymerization is characterized by a decrease in rate with increasing conversion which is most pronounced when the concentrations of oxygen and triethylboron are greatly different. The initial rate of polymerization is proportional to the square root of the oxygen concentration and inversely proportional to the degree of polymerization of poly(methyl methacrylate) formed, confirming the radical nature of the polymerization. The apparent activation energy for the polymerization was unusually low, only 4 kcal./mole. A mechanism in which initiating radicals are produced by a sequence of reactions involving autoxidation of the boron alkyl to peroxide followed by induced decomposition of the peroxide by excess boron alkyl is suggested.
    Additional Material: 5 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3427-3437 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Complexes of vinyldiphenylphosphine oxide, vinyldi-n-butylphosphine oxide, and trans-1-propenyldiphenylphosphine oxide have been prepared with salts of Zn(II), Hg(I), Sb(III), Sn(IV), Ti(IV), Fe(III), and U(VI). The observed shifts in the phosphoryl stretching frequency on complex formation were similar to the values reported for corresponding complexes with triphenylphosphine oxide. The polymerization behavior of these compounds in the presence of free-radical and ionic intiators is similar to that of the unsaturated phosphine oxides themselves. In spite of high salt content, the polymers form clear plaques on molding, and they are completely soluble in appropriate organic solvents.
    Additional Material: 5 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 3439-3449 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Isopropenyldiphenylphosphine oxide (I) and both cis- and trans-n-propenyldiphenylphosphine oxides (II) have been prepared and their structures assigned primarily on the basis of infrared and NMR analyses. Like vinyldiphenylphosphine oxide, these monomers are polymerized sluggishly by free radical catalysts although copolymers with may common vinyl monomers can be prepared. Grignard reagents polymerize (I) very rapidly to low molecular weight products, but the polymerization of II by these catalysts is slower and requires larger amounts of catalyst. Evidence is presented which indicates that in the polymerization of vinyldiphenylphosphine oxide by Grignard reagents molecular weight may be limited by a chain transfer to monomer process.
    Additional Material: 6 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2289-2297 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: When vinyl chloride - methyl methacrylate copolymers having a uniform chain-to-chain composition, are pyrolyzed at temperatures around 150°C., an intramolecular lactonization occurs forming α-methyl-γ-butyrolactone groups in the polymer backbone concomitant with the quantitative elimination of methyl chloride. This reaction has been shown to be a general reaction for copolymers containing α-substituted γ-haloester groups in their backbone. The formation of the lactone groups in these polymers leads to increased chain rigidity and higher polymer softening points. Advantage has been taken of the gaseous alkyl halide elimination to produce rigid vinyl foams of good compressive strengths.
    Additional Material: 3 Ill.
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