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  • Polymer and Materials Science  (4)
  • 42.55  (1)
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  • 1
    ISSN: 1432-0649
    Schlagwort(e): 42.80 ; 42.65 ; 34 ; 42.55 ; 42.70 ; 78
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 703-706 
    ISSN: 0006-3525
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 183-198 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Good yields of some crystalline γ-alkyl esters of L-glutamic acid were obtained by carrying out the esterfication with a small (20-50 mole-%) excess of alcohol in aqueous hydrochloric acid or 60-80% sulfuric acid followed by neutralization with an alkaline solution. This new method made it possible to synthesize various γ-alkyl L-glutamates, including those higher than ethyl, and consequently, various poly(γ-alkyl L-glutamates) such as methyl, ethyl, n-propyl, n-butyl, isobutyl, and isoamyl. The conformation of these poly-L-glutamates in the solid state was determined by the infrared absorption method. The molecular motions of the polymers of γ-methyl, -ethyl, -n-propyl, -n-butyl, and-isoamyl L-glutamates and poly(γ-methyl-D-glutamate) in the solid state were studied by NMR, and dielectric and mechanical measurements. At temperatures up to 400°K., the NMR spectra of poly(γ-methyl D-glutamate) can be explained only by rotational motion of the side chain. Also, from NMR results, rotational motion of C=O groups in the side chain of poly(γ-methyl D-glutamate) is expected near room temperature, and such a motion was examined by dielectric measurements. Rotation of C=O groups in the side chains of polymers of γ-methyl, γ-ethyl, γ-n-propyl, γ-n-butyl, and γ-isoamyl L-glutamate was also observed near room temperature by dielectric measurements in the frequency range from 102 to 106 cps. Activation energies obtained by dielectric and mechanical measurements were similar to those for the side chain motions of the corresponding esters of poly(methacrylic acid). Although it has been noted that the molecular motion of poly(γ-benzyl L-glutamate) in the solid state at room temperature may be related to the motion of its back bone, the molecular motion in these poly-L-glutamates at these temperatures can be explained only in terms of side-chain rotation.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 6 (1968), S. 1065-1081 
    ISSN: 0449-2978
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Conformations of a series of poly(γ-alkyl L-glutamates) (ethyl, n-propyl, n-butyl, isobutyl, and isoamyl) were studied by ORD and infrared absorption methods. All except the n-propyl ester were found to be in helical form in nonpolar non-aromatic solvents such as ethyl acetate, chloroform, ethylene dichloride, methylene chloride, carbon tetrachloride, 2-chloroethanol, dimethylformamide, and dioxane. In such cases, the Cotton effects due to the n-π* transition of peptide bonds occurred near 234 mμ and were of a magnitude similar to those found for poly(γ-benzyl L-glutamate) and poly-L-methionine in nonpolar non-aromatic organic solvents. These four polypeptides in aromatic nonpolar solvents, such as benzene, benzyl alcohol, pyridine, and m-cresol, were also found to be in helical form, although the ORD parameters differed considerably from the values in non-aromatic solvents. An essential cause seems to be the interaction of π electrons on peptide bonds with π electrons in the solvents. Helix-coil transitions of these esters in chloroform-dichloroacetic acid mixtures (dichloroacetic acid seems to be a random coil-forming solvent) were expressed by the Shechter-Blout formulation. This was not true, however, for helix-coil transitions in benzyl alcohol-dichloroacetic acid mixtures. The dependence of the helical stability of these polypeptides in chloroform solution upon the side-chain length and upon temperature is discussed.
    Zusätzliches Material: 9 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 1 (1963), S. 2127-2133 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A series of copolymers of partially neutralized crotonic acid and vinyl alcohol have been prepared with acid monomer contents ranging from 4 to 43 mole-%. The extent of binding of sodium counterions was studied by a transference method employing radiotracers. Comparison of these data with those obtained previously by Nagasawa and Rice for maleic acid copolymers and Wall and co-workers for poly(acrylic acid) gives further support to the contention that the overall charge density on a polyion governs the total counterion binding. Results of potentiometric titrations and viscosity measurements are also reported.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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