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  • 1
    Electronic Resource
    Electronic Resource
    The use of ylide (4-picolinium 4-chloro phenacyl methylide) as an initiator for the polymerization of methyl methacrylate (1985)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 23 (1985), S. 2405-2411 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal polymerization of methyl methacrylate [MMA] was carried out using ylide (4-picolinium 4-chloro phenacyl methylide) as an initiator. The rate of polymerization (Rp) increases with increasing monomer and initiator concentrations; The exponent value has been computed to be 1 ± 0.02 and 0.5, respectively. The reaction was carried out at four different temperatures and the overall activation energy has been computed to be 16.01 kcal/mol. The polymerization was inhibited in the presence of hydroquinone as a radical scavanger. Kinetic studies indicates that the overall polymerization takes place by a radical mechanism.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1985.170230906
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Polymerization initiated by ylide: Polymerization of ethyl methacrylate with the use of 4-picolinium p-chloro phenacylide as initiator (1984)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 22 (1984), S. 1875-1882 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The ylide 4-picolinium, p-chloro phenacylide-initiated thermal polymerization of ethyl methacrylate (EMA) was studied. 4-Picolinium p-chloro phenacylide induces the thermal polymerization of ethyl methacrylate at 65°C. The rate of polymerization (Rp) rose as the initiator concentration increased from 2 × 10-3 to 4 × 10-3 M and the initiating exponent was computed as 1.9. The Rp decreased as the concentration of ylide increased from 6 × 10-2 to 1M. The greater initiator concentration also affected the molecular weight inversely. The polymerization was carried out at different temperatures and the overall activation energy was computed as 4.08 Kcal/mol. Polymerization was inhibited in the presence of hydroquinone as a radical scavenger. Kinetic studies and other data show that the overall polymerization takes place in a radical mechanism. The various kinetic parameters, such as the rate and average degree of polymerization, molecular weight, and energy of activation of the present system, were evaluated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1984.170220809
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    p-acetyl benzylidene triphenylarsonium ylide initiated radical terpolymerization of styrene, acrylonitrile and copper acrylate: synthesis, characterization and properties (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 407-412 
    Details
    ISSN: 0959-8103
    Keywords: terpolymerization ; kinetics ; thermal properties ; arsonium ylide ; styrene ; acrylonitrile ; copper acrylate ; 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: Solution terpolymerization of styrene (Sty), acrylonitrile (AN) and copper acrylate (CuA) has been carried out in dimethylformamide at 90°C for 4 h using p-acetyl benzylidene triphenylarsonium ylide as radical initiator. 1H nuclear magnetic resonance (NMR), IR and elemental analysis have been used to characterized the terpolymer. Analysis of kinetic data indicates the following rate equation: $$R_{\rm p} \propto \left[ {{\rm ylide}} \right]^{0.5} \left[ {{\rm Sty}} \right]\left[ {{\rm AN}} \right]{1 \over {\left[ {{\rm CuA}} \right]}}$$ The overall activation energy is 38 kJ mol-1. The composition of terpolymer calculated from NMR and elemental analysis has been used to evaluate reactivity ratios as r1(Sty) = 5 ± 2 and r2(AN + CuA) = 0.4 ± 0.02 employing the Finemann-Ross method, which confirms its random origin. The terpolymer was thermally stable up to 2007deg;C.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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    Paper (German National Licenses)
  • 4
    Electronic Resource
    Electronic Resource
    Copolymerization of zinc acrylate with acrylonitrile initiated by As2S3-styrene complex (1994)
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 34 (1994), S. 105-109 
    Details
    ISSN: 0959-8103
    Keywords: Zinc acrylate ; acrylonitrile ; As2S3-styrene complex ; copolymerization ; dilatometry ; kinetics ; 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: Radical copolymerization of zinc acrylate (ZnA2) with acrylonitrile (AN), initiated by As2S3-styrene complex(I), in dimethyl Sulphoxide (DMSO) at 90 ± 0.1°C for 1.0h under inert atmosphere, yields non-alternating copolymers. The kinetic expression is Rp ∝ [I]0.33 [ZnA2]0.25 [AN]0.44, i.e. the system follows non-ideal kinetics, which is due to primary radical termination as well as degradative chain transfer reactions. The values for activation energy (E) and k2p/kt are 128kJ mol-1 and 8.57 × 10-7 litre mol-1 s-1, respectively. Thermal stability, solubility in different solvents, and IR and NMR spectra have been evaluated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pi.1994.210340114
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    Paper (German National Licenses)
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