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  • 1
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Water-soluble, random copolymers containing L-methionine and N5-(3-hydroxypropyl)-L-glutamine have been prepared, fractionated, and characterized. The thermally induced helix-coil transitions of these copolymers in water have been investigated, and it has been found that incorporation of L-methionine increases the helix content of the polymers at all temperatures in the range of 0-60°C. The Zimm-Bragg parameters σ and s for the helix-coil transition in poly(L-methionine) in water were deduced from an analysis of the melting curves of the copolymers using the methods described in earlier papers.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Previously used procedures for processing the amino acids from 6N hydrochloric acid hydrolysis of poly[N5-(4-hydroxybutyl)-L-glutamine], poly[N5-(3-hydroxypropyl)-L-glutamine], and several random copolymers derived from these, led to the formation of spurious products. These have been isolated and characterized as the γ-ester of glutamic acid and the hydroxyalkyl amine, and chloro-alkyl amine hydrochloride. The former reduces the observed values for glutamic acid, but the latter has no effect on them. A method is used to avoid formation of these artifacts in the amino-acid analysis. Of all the copolymers studied previously in this series, the compositions of only those containing L-serine are in error as a result of the formation of the γ-ester. A redetermination of the amino-acid compositions of the copolymer fractions studied earlier leads to slightly revised values for the Zimm-Bragg parameters σ and s of serine.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 2469-2480 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The amino-acid-sequence distribution in poly(γ-benzyl-L-glutamate, L-methionine) prepared by polymerization of the respective N-carboxyanhydrides has been investigated. This copolymer was converted first to poly(L-glutamic acid, L-methionine), which was subsequently cleaved by treatment with cyanogen bromide. The resulting material was fractionated into oligomers of (glutamic acid)n-homoserine whose relative molar amounts were determined quantitatively. The results have been compared with those for a random incorporation of the methionine in a γ-benzylglutamate host polymer. Fairly close agreement has been found.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 20 (1982), S. 241-244 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A simplified approximation method for the treatment of dead-end and high conversion polymerization kinetics is presented. The method is based on the treatment of dead-end polymerization first described by Tobolsky. In appropriate circumstances, by contrast with Tobolsky's method, this method provides measurements of kd and kp/kt1/2 without recourse to the measurement of the monomer conversion at infinite time.Kinetic studies of free radical polymerizations are normally confined to measurements of initial rates. At low conversions the predictions of the general mechanism for chain-growth polymerization involving initiation, propagation, and termination steps are generally obeyed. Thus the polymerization rate should be first order in the vinyl monomer and half-order in the initiator concentrations.At high conversions, however, large deviations which can be ascribed to various effects can occur; for example, (1) the effect of the increasing viscosity of the polymerization medium on the termination rate constant kt, and possibly also on the propagation rate constant kp, which have been considered by North1 and Cardenas and O'Driscoll,2 or (2) depletion of the initiator as the polymerization progresses. This depletion will occur in all polymerizations but its significance will depend on the magnitude of the rate constant for initiator decomposition (kd) and the period of polymerization. Appropriate conditions will lead to limiting monomer conversion even after infinite polymerization time; this phenomenon has been called dead-end polymerization by Tobolsky.3Free radical polymerizations to high conversion are particularly important in the industrial context when initial kinetics are obviously inadequate. Suitable treatment of the conversion/time relationship is highly desirable.Senogles and Woolf4 have examined the polymerization of n-lauryl methacrylate at 60°C with 2-azobisisobutyronitrile as initiator under dead-end conditions.Here we propose a modification of Tobolsky's treatment of such polymerizations by using an approximation for the exponential decay in the initiator concentration. This method permits easy manipulation of the experimental data and the estimation of values for the kinetic parameters in favorable circumstances without recourse to the measurement of the conversion at infinite time or the evaluation of complicated functions of the monomer conversion. The method thus allows the duration of the laboratory experimentation to be significantly shortened and the complexity of the subsequent data analysis to be considerably reduced.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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