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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 28 (1995), S. 8051-8056 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1022-1352
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The atom transfer radical polymerization (ATRP) of styrene has been studied using complexes of copper carboxylates. Compared with systems employing copper halides as the catalyst, the use of the copper carboxylates resulted in faster polymerization rates and higher polydispersities. A ligand (dNbpy) to Cu(I) carboxylate ratio of 1 was sufficient to achieve the maximum rate of polymerization. The addition of a small amount of either Cu(II) or Cu(I) halide to the copper carboxylate system yielded polymers with better controlled molecular weights and lower polydispersities yet the polymerization still remained relatively fast.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 823-830 
    ISSN: 0887-624X
    Keywords: atom transfer radical polymerization ; poly(N-vinylpyrrolidinone-g-styrene) ; macromonomer method ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Atom transfer radical polymerization has been used to prepare well-defined vinyl macromonomers of polystyrene using vinyl chloroacetate as an initiator. Because styrene and vinyl chloroacetate do not copolymerize, no branching or incorporation of the initiator into the backbone was observed. Macromonomers of several molecular weights were prepared and copolymerized free radically with N-vinylpyrrolidinone in varying feed ratios in order to produce poly(NVP-g-Sty) graft copolymers. The macromonomers used were of sufficiently high molecular weight to form physical crosslinks in solvents which favor the hydrophilic NVP, such as water, which prevent the copolymer from dissolving and cause it to swell. These materials, therefore, formed hydrogels of swellabilities in water exceeding 95%, depending on the amount of styrene that was incorporated into the copolymer. Limitations of and alternatives to this method are also discussed. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 823-830, 1998
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 1057-1066 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Mono and difunctional polystyrenes containing active halogenated end groups were prepared by atom transfer radical polymerization (ATRP). Substitution reactions were explored to convert the halogen termini to azido groups, followed by readuction to form the amino functional polymer. Quantitative conversion of the end groups was observed in each transformation reaction. 1H NMR demonstrated the formation of the azide from the bromide functionality without elimination. The difunctional α,ω-diaminopolystyrene was reacted with terephthaloyl chloride in a condensation process to produce chain-extended polystyrene containing amide bonds along the polymer backbone.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Graft copolymers of poly(vinyl chloride) with styrene and (meth)acrylates were prepared by atom transfer radical polymerization. Poly(vinyl chloride) containing small amount of pendent chloroacetate units was used as a macroinitiator. The formation of the graft copolymer was confirmed with size exclusion chromatography (SEC), 1H NMR and IR spectroscopy. The graft copolymers with increasing incorporation of butyl acrylate result in an increase of molecular weight. One glass transition temperature (Tg) was observed for all copolymers. Tg of the copolymer with butyl acrylate decreases with increasing content of butyl acrylate.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 19 (1998), S. 665-670 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The addition of zero-valent copper to the self-condensing vinyl polymerization (SCVP) of novel AB* (meth)acrylic monomers using atom transfer radical polymerization (ATRP) catalyst systems has allowed for their successful polymerization. Polymerization under homogeneous and heterogeneous catalyst conditions without additional Cu(0) were unsuccessful. The catalyst system that was designed comprised of Cu(I) bromide, 4,4′-bis(5-nonyl)-2,2′-bipyridine, and Cu(0) metal (powder or turning). From 1H NMR spectroscopy, the degree of branching was estimated for the acrylic polymers, DB = 0.48. The degree of branching could not be determined for methacrylates by this method due to overlapping signals in the 1H NMR spectra.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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