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  • 1975-1979  (3)
  • Physics  (3)
  • Organic Chemistry
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 1721-1735 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The new oxazoline-containing monomers, 4-acrylyloxymethyl-2,4-dimethyl-2-oxazoline (AOMO), 4-methacrylyloxymethyl-2,4-dimethyl-2-oxazoline (MAOMO), 4-methacrylyloxymethyl-2-phenyl-4-methyl-2-oxazoline (PMAOMO), and the previously known monomer, 2-isopropenyl-4,4-dimethyl-2-oxazoline (IPRO), were synthesized for addition polymerization studies. The monomers were homopolymerized in benzene using a free radical initiator and in aqueous media using emulsion techniques. Molecular weights of 8,000-15,000 (M̄w) were obtained for the homopolymers. Copolymerization studies were carried out with AOMO, MAOMO, and IPRO as M1, and methyl methacrylate (MMA), methyl acrylate (MA), styrene (STY), acrylonitrile (AN), and vinyl acetate (VA) as M2 for each case of M1. Relative reactivity ratios for the fifteen copolymers and Q and e values for the three oxazoline monomers were determined. The r1 values for AOMO and MAOMO copolymerizations indicated a lower value of k11 than expected, presumably because of steric effects. The r1 values in the IPRO copolymerizations were somewhat larger than expected. It was proposed that significant electron donation to the radical center of IPRO·by resonance effects occured.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 13 (1975), S. 39-47 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Polytetramethyl-p-silphenylenesiloxane (I) and polymethylphenylsiloxane (II) were prepared and subsequently reacted with hexacarbonylchromium to generate their n6-Cr(CO)3 complexed analogs, III and IV, respectively. During the complexation reaction, completing decomposition to chromium salts took place. Furthermore a competing chain scission reaction took place resulting in lower molecular weights for the complexed polymers. Heating III and IV resulted in carbon monoxide evolution and the presence of n6-Cr(CO)3 moieties lowered the thermal stability of the polymers.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1715-1734 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The solution polycondensation of 1,4-bis(hydroxydimethylsilyl)benzene with six bis(dimethylaminosilanes) was carried out by the aminosilane deficient method to give a series of high polymers. The bis(dimethylaminosilanes) were bis(dimethylamino)dimethylsilane, bis(dimethylamino)methylphenylsilane, bis(dimethylamino)diphenylsilane, 1,4-bis(dimethylaminodimethylsilyl)benzene, 1,3-bis(dimethylamino)-1,1,3,3-tetramethyldisiloxane, and 1,5-bis(dimethylamino-1,1,3,3,5,5-hexamethyltrisiloxane). The condensation of dihydroxymethylphenylsilane with bis-(dimethylamino)methylphenylsilane to give polymethylphenylsiloxane was also performed. A detailed description of the monomer syntheses and polymerization reactions is provided, since this paper represents the first detailed and systematic description of this polycondensation as an alternative to disilanol or disilanol-dichlorosilane condensation routes. The thermal properties (i.e., Tg, TGA, DSC) of poly(p-phenylenetetramethylsiloxane) are compared to those of poly[1,4-bis(oxydimethylsilyl)benzenel] (where a —Si(Me)2O— group has been inserted between the silylphenylene units) as well as others in this series, polydimethylsiloxane, and polymethylphenylsiloxane. Similarly, these properties are compared with those of related polymers which include in-chain ferrocene units. Introduction of —Si(Me)2O— units into poly(tetramethyl-p-silylphenylenesiloxane) systematically decreases Tg and thermal stability. Replacing Si—CH3 with Si—C6H5 groups increases Tg and thermal stability. Replacing in-chain —C6H4— with ferrocene increases Tg and slightly decreases thermal stability. The values of K and A in the Mark-Houwink equation were determined for several polymers.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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