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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 190 (1989), S. 2287-2291 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The copolymerization of styrene (St) with acrylonitrile (AN) initiated with 2-methyl-2-undecanethiol (RSH) was investigated. Kinetic studies revealed that the initial rate of the copolymerization, which does not occur spontaneously in the absence of RSH, obeys the following expression: Rp ∝ [RSH]x, where x is 0,5 when [RSH] ranges from 3,4.10-4 to 3,4.10-3 mol/l and 0 when [RSH] is larger than 3,4.10-3 mol/l. The initial copolymerization rate, Rp, increases with increasing percentage of AN in the monomer feed. From the slope of ln Rp vs. 1/T, the apparent activation energy, Eapp, was calculated to be 17 kJ/mol in the temperature range of 30°C to 50°C. RSH is the only initiating species, and it also plays a role as chain-transfer agent. The value of Mw/Mn, which varies from 1,5 to 2,0, is typical of a free-radical poymerization. The reactivity ratios were calculated to be rSt = 0,42 ± 0,04 and rAN = 0,02 ± 0,03. It seems to be unnecessary to introduce a penultimate effect for explaining the experimental data.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 30 (1992), S. 2181-2185 
    ISSN: 0887-624X
    Keywords: copolymerization ; charge-transfer complex ; styrene ; N-phenyl maleimide ; thiol ; alternative copolymer ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Methyl-2-undecanethiol was found efficient to initiate the free-radical copolymerization of styrene (St) with N-phenyl maleimide (NPMI) at 40°C. The initial copolymerization rate increases with the increasing of thiol concentration at first, then keeps constant with the further increasing of the thiol concentration. The charge-transfer complex (CTC) formed between St and NPMI was investigated in different solvents by using 1H-NMR. There is no definite correlation between CTC equilibrium constant, K, and the polarity of the solvent. With the increasing of CTC concentration, both the copolymerization rate and NPMI content in copolymer enhances, indicating the participation of CTC in both initiation and propagation. The monomer reactivity ratios were calculated to be rNPMI = 0.052 and rSt - 0.166, showing an alternating tendency for the copolymerization of St with NPMI. The molecular weight approach has shown again the effect of CTC. The function of thiol as a regulator is mitigated due to the involvement of CTC. © 1992 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Basel : Wiley-Blackwell
    Die Makromolekulare Chemie, Rapid Communications 10 (1989), S. 31-34 
    ISSN: 0173-2803
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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