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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 15 (1977), S. 2059-2065 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oxidation of hydroquinone catalyzed by copper(II) complexes of poly-1-vinylimidazole, vinylamine-vinylacetamide copolymer, and polyethyleneimine was studied in aqueous solution at 25°C. The rate of oxidation was determined spectrophotometrically over several pH values. The rate of copper(II) reduction was evaluated from copper(I)-cuproin complex formation, and the reoxidation of copper(I) to copper(II) was observed by visible spectroscopy. Among the copper(II) complexes, poly-1-vinylimidazole complex exhibited excellent catalytic activity, which amounted to over 20 times that of aqueous copper(II) ion solution, while the reduction of copper(II) in the former system was slower than that in the latter system. The reoxidation of copper(I) to copper(II) was found to be completed immediately in the presence of polymer ligands such as poly-1-vinylimidazole, while copper(I) ion was only slowly reoxidized. The discussion of the reaction mechanism emphasizes the importance of the reoxidation process.
    Additional Material: 4 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 17 (1979), S. 2729-2737 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The autoxidation of Cu(I) complexes with imidazole and polyvinylimidazole derivatives was studied by observing the formation of the corresponding Cu(II) complexes with a stopped-flow technique. The reaction was second order and proportional to the concentrations of Cu(I) and oxygen. In the Cu(I)-imidazole complex pH variation was without effect in the range of 7.5-8.6. The oxidation rate of Cu(I).polyvinylimidazole complexes, on the other hand, decreased with a rise in pH. The activation parameters of the Cu(I)·polyvinylimidazole complexes, compared with those of the Cu(I).imidazole complex, were characterized by large enthalpic requirements coupled with favorable entropies of activation. This was explained by the fact that a conformational change in the polymeric ligands took place during oxidation.
    Additional Material: 7 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 18 (1980), S. 101-107 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Cu(II) complexes of copolymers having pendant sulfide and imidazolyl groups were prepared by a free radical copolymerization of ethylvinylsulfide with vinylimidazole, and their properties and function were studied spectrophotometrically in comparison with those of poly[4(5)-vinylimidazole]. The complexes were found to be effective as catalysts for the oxidation of hydroquinone. Visible and ESR spectra of the Cu(II)-copolymer complexes were similar to those of the Cu(II)-homopolymer complexes, while the catalytic activity for the oxidation was different between these complex systems. A rapid reaction followed by a slow reaction, particularly at high ethylvinylsulfide content in the copolymers, was observed in the Cu(II)-copolymer complex systems, but a continuous reaction proportional to the reaction time was observed in the Cu(II)-homopolymer complex systems. The reoxidation rate of Cu(I) to Cu(II) complex, which was little affected by the concentration of imidazolyl group, decreased with a rise of the ethylvinylsulfide content in the copolymer. It was suggested that the sulfur atom of the sulfide group was weakly coordinated to Cu(II) but strongly to Cu(I), and an electron transfer reaction from substrate to the Cu(II) complex was increased, while reoxidation reaction of the Cu(I) complex was decreased in the copolymer complex systems.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 25 (1980), S. 731-738 
    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 ability of adsorbing iodine in different organic solutions by chitosan was studied by sorption isotherm measurements. The ability was found to be larger in polar solvents than in nonpolar solvents. The form of the chitosan samples, such as film, powder, and flake, had no influence on the adsorption behavior. On the other hand, chitin had only small adsorbing ability of iodine. It is concluded that the adsorption of iodine is caused by charge - transfer complexes between aminogroups of chitosan and iodine molecules, but their structure differs from that of inclusion compounds as seen in amylose-iodine complexes. The adsorption was also studied on chitosan films with different degrees of acetylation.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 5
    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 cationic polymerization of 1,2-butylene oxide initiated by radical catalysts has been investigated in detail in the presence of maleic anhydride. The active species of this ionic polymerization was thought to be a conjugated radical of poly(maleic anhydride).
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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: In a previous paper1 it was mentioned that trapped radicals in poly(maleic anhydride) (Poly-MAH) have the ability to initiate cationic polymerization. In this paper, the cationic polymerization of isobutyl vinyl ether (IBVE) is described using Poly-MAH as the initiator. These radicals show different behavior during polymerization depending upon their structure. In particular, large conjugated radicals initiate ionic polymerizations.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The effect of ionic strength on the structure of Cu(II) complexes of imidazole and poly(4(5)-vinylimidazole) in aqueous solution was studied by viscometric, spectrophotometric, and electron spin resonance (ESR) techniques. Frequency of the center of the absorption band in visible region (λmax) and ESR spectra of the polymeric Cu(II) complex were different from those of the low-molecular-weight Cu(II) complex. The spectra of polymeric Cu(II) complex were different in the presence of sodium perchlorate, but it was not the case for the low-molecular-weight Cu(II) complex. The reduced viscosity of the polymeric Cu(II) complex and the polymeric ligand decreased with a rise of the concentration of sodium perchlorate. It was proposed that the conformational change in the polymeric ligand resulted in a structural change of the Cu(II). poly(4(5)-vinylimidazole) complex.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 517-525 
    ISSN: 0887-6266
    Keywords: positron annihilation in polyethylene, before and after irradiation ; polyethylene, positron annihilation in, effect of radiation on ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Positron lifetimes were measured for four kinds of polyethylene samples and were resolved into four components. The temperature dependence of the two longlived components was examined in detail. In agreement with other results, the longest lived component could be reasonably assigned to ortho-positronium located in amorphous regions. This component was shown to be sensitive to the defects in high-density polyethylene introducted in the course of its production. Both the intensity and the lifetime of the second longest lived component were structure insensitive, i.e., they did not change even on passing through the melting point. This component has been tentatively assigned to a positronium compound state. The effect of gamma-ray irradiation was also examined. Although the intensity (I4) of the longest lived component was reduced by the irradiation, correlation between I4 and the free radical concentration was poor, and the reduction in I4 caused by the irradiation is considered to be due to structure change and not to chemical reasons.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 49 (1993), S. 1921-1929 
    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: Four kinds of epoxy resins: cresol novolac, tris-hydroxyphenylmethane, tetramethylbiphenol, and bisphenol A, were cured with phenol novolac epoxy resins. Characteristics of these epoxy compounds were studied by the positron annihilation lifetime (PAL) technique. Glass transition temperatures, thermal expansion coefficients, and volume of intermolecularspace holes among polymer chains were obtained from the lifetime, τ3, of the long-lived component of ortho-positronium. It was revealed that, at the glass transition temperature, Tg, the volume of the hole created among polymer chains expanded 1.4 times the volume at room temperature. The smaller flexural modulus of tris-hydroxyphenylmethane than that of the other samples was explained by the volume of intermolecular-space holes obtained from τ3. Aging effects were seen in the data of the intensities, I3, of ortho-positronium, which became smaller after heating the samples above Tg. I3 and τ3 were strongly affected by the density of cross-linkings, and their chemical structures. The larger the density of cross-linkings, the smaller I3 and higher Tg were obtained. Epoxy compounds with the higher water-absorption rates had larger intermolecular-space holes. © 1993 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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