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  • Polymer and Materials Science  (2)
  • Analytical Chemistry and Spectroscopy  (1)
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  • Polymer and Materials Science  (2)
  • Analytical Chemistry and Spectroscopy  (1)
  • Chemistry  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 54 (1961), S. 329-342 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Methacrylic anhydride was polymerized, in high yields, at temperatures ranging from 1 to 80°, in benzene solution, to linear, soluble polymers. The polymethacrylic anhydride so prepared was hydrolyzed to the corresponding polymethacrylic acid and this poly(acid) esterified by reaction with diazomethane to yield polymethyl methacrylate. The result is given of an x-ray diffraction study of an unstretched film of polymethyl methacrylate prepared in a similar manner. The determination of the fraction of the polymer present in each of the three possible stereoconfigurations, isotactic, syndiotactic, and heterotactic, was made from a nuclear magnetic resonance investigation of the derived polymethyl methacrylate. The results indicate that the stereoconfiguration is influenced by the cyclic polymerization mechanism. The results also indicate that there is a bias toward increasing isotactic character in the polymers with an increase in polymerization temperature. Two possible explanations are offered: one in terms of a kinetic control of the steric placements and the other in terms of a balance between equilibrium and kinetic considerations.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 17 (1981), S. 290-295 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Natural abundance proton-coupled 15N NMR spectra have been observed for pyridine and a series of mono- and disubstituted pyridines using polarization transfer achieved by the selective population transfer method. The magnitudes and signs of the 15N—1H spin-spin coupling constants between the ring-nitrogen and ring-protons are determined from complete iterative spectral analysis and/or selective population transfer experiments. Substituent effects on the 15N—1H coupling constants are discussed and compared with those for 13C—1H couplings in substituted benzenes.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 1-Methylene-4-vinylcyclohexane was prepared by the following reaction sequence: (1) conversion of 4-methylene-cyclohexane methanol to the tosylate, (2) oxidation of the tosylate to 4-methylenecyclohexane carboaldehyde by the method of Kornblum, and (3) reaction of the aldehyde with the ylide from triphenylmethylphosphonium bromide in a Wittig reaction to produce the diene. Polymerization of 1-methylene-4-vinylcyclohexane was attempted with the use of free radical, anionic, cationic, and Ziegler-type initiators. Polymers were obtained from the cationic (boron trifluoride) and Ziegler (titanium tetrachloride and triethylaluminum complex)-initiated reactions. The polymer obtained by polymerization of this monomer with gaseous boron trifluoride as the initiator led to a solid polymer which was soluble in a number of organic solvents and had a softening temperature of 150°C. The infrared spectrum of this polymer gave absorption bands for terminal unsaturation. NMR analysis indicated that the unsaturation ratio was one double bond per two monomer units. The NMR analysis also indicated that this unsaturation was due to vinyl rather than methylene groups. Polymerization of this monomer by use of a Ziegler catalyst (titanium tetrachloride and triethylaluminum) led to a solid polymer of which 10% was soluble in a number of organic solvents. Although the infrared spectrum of this polymer indicated the presence of some terminal unsaturation, an NMR analysis indicated only an extremely small amount of residual unsaturation. The essential absence of unsaturation in this linear polymer supports an intramolecular interaction in this monomer, since Ziegler-type initiators do not ordinarily initiate polymerization of the isobutylene type. These results can be interpreted as additional evidence for the nonbonded interaction concept as a driving force to cyclic polymer.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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