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  • Physics  (4)
  • template polymerization  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Template polymerization of multiacrylate (1994)
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 32 (1994), S. 295-300 
    Details
    ISSN: 0887-624X
    Keywords: multiacrylate ; template polymerization ; ladder polymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: By reacting poly (2-hydroxyethyl methacrylate) with acryloyl chloride, multiacrylate connected through a covalent bond with polymethacrylate chain (template) has been obtained. The free-radical polymerization of multiacrylate in dilute dioxane solutions at 75°C and 85°C was examined by IR spectrophotometry and the distribution of molecular weights of the resultant products was evaluated by gel permeation chromatography. The findings show that under selected conditions the polymerization proceeds along ordered acrylic double bonds on the template and results in a ladder-type polymer. At a temperature of 85°C, in addition to the intramolecular cyclopolymerization, intermolecular reactions proceed to a minor extent. © 1994 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pola.1994.080320210
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  • 2
    Electronic Resource
    Electronic Resource
    Investigation of the viscosity of solutions of graft copolymers (1967)
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 5 (1967), S. 891-898 
    Details
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Living polystyrene was grafted on fractions of poly(methyl methacrylate) by an anionic grafting reaction. Unreacted polystyrene was separated by fractional precipitation. The composition of copolymer, i.e., the molecular weight of main chains and side chains, was determined. The influence of molecular weight and structure of graft copolymers on the intrinsic viscosity of solutions was examined. This may be expressed in the form [η] = KMagn. The dependence between a and n in this equation was established.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1967.160050507
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  • 3
    Electronic Resource
    Electronic Resource
    Composition equation for matrix copolymerization (1984)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 2887-2894 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A mechanism of matrix copolymerization in which a monomer (or macroradical) is complexed by matrix was considered. For this case a composition equation was formulated. It was shown that in general case reactivity ratios are dependent on the matrix concentration. The influence of the critical length of a complexed radical on the process of copolymerization is also discussed. A series of copolymerizations of methacrylic acid and styrene were carried out using various compositions of initial monomer mixtures. The process was performed in benzene in the presence of poly(ethylene glycol) as a matrix. The copolymerization were carried out at various ratios of the monomer being complexed (methacrylic acid) to the matrix. Compositions of the complexes prepared were determined by the NMR method. Reactivity coefficients for both monomers were found and the results are discussed on the basis of the derived equation.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1984.170221113
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  • 4
    Electronic Resource
    Electronic Resource
    Substituent effect on the hydrolysis of side groups in poly(phenyl methacrylates)This work was presented in part at the IUPAC Symposium in Bratislava, July 3-6, 1979. (1982)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 3267-3270 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The kinetics of the basic hydrolysis of several poly(phenyl methacrylates) with different substituents in the aromatic ring were investigated. Using Keller's equations to describe the effect of neighboring groups on the kinetics of side-group reactions in polymers, we computed the corresponding rate constants which correlated well with Hammett's substituent constants.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1982.170201201
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  • 5
    Electronic Resource
    Electronic Resource
    Kinetics of hydrolysis of side groups in polyphenylmethacrylateThis work was presented in part at the IUPAC Symposium in Tashkent, October 17-21, 1978. (1981)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 19 (1981), S. 51-55 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ultraviolet (UV) spectrophotometry was used to study the kinetics of basic hydrolysis of side groups in polyphenylmethacrylate in DMSO/H2O at various temperatures. Keller's mathematical analysis was applied to the description of the kinetics. Three rate constants which describe the reaction of ester groups with 0, 1, and 2 reacted neighboring groups, respectively, were determined. Activation energies for the hydrolysis reaction of the respective triads were calculated. The data confirmed the applicability of Keller's model to the computation of rate constants for the reaction of the respective triads in the polymer chain.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1981.170190106
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