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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 258-272 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The isobutylene (IB)-p-methylstyrene (pMeSt) monomer pair readily produces by living copolymerization nearly random copolymers with up to M̄n ≈ 50,000 g mol-1 and M̄w/M̄n ≈ 1·4. The livingness of the copolymerization process and the compositional homogeneity of the copolymers have been demonstrated by the following four diagnostic plots: (A) M̄n (number-average molecular weight) and corresponding N (number of moles of copolymer formed) vs Wp (weight of copolymer formed) for the diagnosis of chaintransfer; (B) -ln (1 - C) (C = conversion of monomers) vs time for the diagnosis of termination; (C) copolymer composition vs molecular weight; and (D) cumulative copolymer composition vs conversion for the diagnosis of true homogeneous copolymers. The theory for the use of the -ln(1 - C) vs time plot for the quantitation of irreversible termination in copolymerization has been developed. The exact conditions (i.e. nature of reagents, reagent concentrations, temperature, etc.) which lead to desirable products in terms of conversion, molecular weight, molecular weight distribution (MWD) and copolymer composition, were developed systematically by analyzing the results of a large number of experiments. The following combination of chemicals was found to lead to living copolymerization, and uniform high molecular weight, narrow MWD copolymers: IB-pMeSt 97 : 3 mol/mol with 5-tert-butyl-1,3-dicumyl methyl ether (5-tBu-1,3-DiCumOMe) initiator, TiCl4 coinitiator, ethyl chloride (EtCl) solvent, triethylamine (TEA) electron pair donor (ED) and 2,6-di-tert-butylpyridine (DtBP) proton trap at -52, -65 and -85°C.
    Additional Material: 13 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 8 (1995), S. 273-281 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A novel method was developed for the quantitative description of copolymerization behavior, specifically for the derivation of reactivity ratios and micro- and macro-compositions of monomer pairs with significantly different reactivities. The novelty of the method lies in the manner of generating instantaneous feed and copolymer composition data from experimentally readily obtainable cumulative copolymer compositions, although the latter drifts with progressing copolymerization. It is demonstrated that such copolymer systems can be described by two reactivity ratios, albeit the values are valid only over the narrow feed composition range within which they were determined. The great advantage of this method is that whereas the differential copolymer composition equation is strictly valid only at 0% conversion, the method produces corresponding instantaneous feed and copolymer compositions at any conversion. Assumptions or approximations are unnecessary to calculate reactivity ratios. Subsequently the procedure was applied to obtain reliable monomer reactivity ratios of isobutylene (IB)-p-methylstyrene (pMeSt) copolymers, rIB and rpMest, prepared by living carbocationic copolymerizations with [IB]/[pMeSt] feeds compositions of 90:10 and 97:3 mol/mol, i.e., with feed compositions of industrial importance. According to our procedure, rIB = 0·74±0·11 and rpMeSt = 7·99±3·34. These reactivity ratios were then used to calculate overall IB-pMeSt copolymer compositions over the entire comonomer conversion range and to compare calculated with experimental compositions. The good quantitative agreement between calculated and experimental compositions indicates that the description of both macro- and micro-compositions of IB-pMeSt copolymers obtained in the 90:10 and to 97:3 mol/mol feed composition range is satisfactory.
    Additional Material: 13 Ill.
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  • 3
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A redetermination of the disproportionation/combination ratio for n-C3F7 and C2H5 radicals gives a value of Δ(n-C3F7, C2H5) = 0.13 ± 0.01, independent of the temperature. The radicals were produced by the photolysis of n-C3F7COC2H5. The previous determinations of this ratio are discussed and are found to be largely incorrect. The values for Δ(CF3, C2H5) and Δ(C2F5, C2H5) are also re-evaluated, and the recommended values are 0.10 ± 0.02 and 0.12 ± 0.02, respectively. Systems involving perfluoroalkyl and ethyl radicals are complicated due to rapid perfluororadical addition to the ethylene formed in the disproportionation process. The extent of this reaction, and its consequences, are discussed and evaluated. The role of the propionyl (C2H5CO) radical in the room temperature photolysis is also assessed. However, it is found that the Δ values determined by the intercept method used in this work are not affected by the secondary reactions that occur. It is concluded that high cross-combination ratios are general to perfluoroalkyl-alkyl radical interactions. For C3F7 and C2H5 radicals the ratio is 2.7-2.8. Above 100°C ratios exceed 3 due to secondary reactions.
    Additional Material: 4 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 23 (1991), S. 103-103 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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