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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 183 (1982), S. 863-874 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The free radical polymerization of N-vinylcarbazole (VK) was investigated in hexane, nonane, toluene, HMPT, DMF, DMAC, and DMSO. Isotactic propagation was found to be energetically favoured by between 1500 and 4600 J · mol-1 for all the solvents investigated, although the entropy difference between syndiotactic and isotactic propagation strongly favoured syndiotactic propagation by between 11 and 20 J · mol-1K-1. Variation in the steric microstructure between an isotactic mole fraction of 0,25 and 0,47 was obtained by varying the polymerization temperature and solvent. The activation enthalpy differences between isotactic and syndiotactic propagation (ΔH≠s/i - ΔH≠i/s), for the free radical polymerization of methyl methacrylate (MMA) and VK were compared and the steric configurations involved in the propagation process considered. It was concluded that electronic interaction between radical and monomer appeared to determine the energetic preference of the growing chain for isotactic or syndiotactic propagation in free radical propagation. This energetic preference was correlated with the e-factor in the Q - e scale. Data for the free radical polymerization of VK, MMA, and vinyl trifluoroacetate showed that solvent polarity has a weak influence on the energetic preference of the growing chain for isotactic or syndiotactic propagation. This energetic preference was correlated with the π* solvent polarity scale.
    Additional Material: 7 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 20 (1982), S. 2529-2543 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dependence of the steric microstructure of cationically polymerized poly(N-vinylcarbazole) (PVK) upon catalyst, polymerization temperature, and polymerization solvent has been investigated. The effect of polymerization temperature variation was found to be small, whereas the choice of catalyst and polymerization solvent was found to have a strong influence upon the PVK steric microstructure. A correlation was found between the syndiotacticities Xs and the π* solvent polarities of the polymerization solvents for a given catalyst. A decrease in Xs with increasing π* solvent polarity was observed using BF3OEt2 and AlEt2Cl catalysts and has been interpreted in terms of propagation via contact ion-pair ring structures reversibly formed between the active end group and a preceding repeating unit. The increase in Xs with increasing π* solvent polarity observed with several of the catalysts investigated has been interpreted in terms of chain ion pairs whose separation increases with increasing π* solvent polarity. The influence of the various Lewis acid catalysts upon the steric microstructures of cationically polymerized PVK allowed the following order of nucleophilicity to be established: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm TiCl}_{\rm 4} 〉 {\rm SnCl}_{\rm 4} 〉 {\rm AlEt}_{\rm 2} {\rm Cl} 〉 {\rm BF}_{\rm 3} {\rm OEt}_{\rm 2} 〉 {\rm ZnCl}_{\rm 2} $$\end{document}
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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