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  • 1980-1984  (3)
  • 1-hexanol  (1)
  • Solvent-induced conformational change  (1)
  • counter-ion binding  (1)
  • heptanesulfonate  (1)
  • sodium octanoate  (1)
Materialart
Erscheinungszeitraum
  • 1980-1984  (3)
Jahr
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 261 (1983), S. 591-599 
    ISSN: 1435-1536
    Schlagwort(e): Copoly (N 5-ω-hydroxyalkyl-L-glutamine-L-glutamic acid) ; Solvent-induced conformational change ; pH-induced conformational change
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract Copoly (α-amino acid)s consisting ofL-glutamic acid residue andN 5-ω hydroxyalkyl-L-glutamine residue, i.e., 2-hydroxyethyl, 3-hydroxypropyl, and di-2-hydroxyethyl derivatives were prepared by the reactions of copoly (L-glutamic acid) containing succinimide ester with corresponding amino alcohols. The conformation of these copolymers was examined by the CD and infrared measurements. These three copolymers containing about 20–30% hydroxyalkyl groups undergo a methanol-induced and a pH-induced conformational transitions. The copolymer containing about 50% 3-hydroxypropyl group assumes the α-helical conformation in the pH region from 2.5 to 11.6, and in a methanol-water mixture (9∶1). On the other hand, the copolymer containing about 60% di-2-hydroxyethyl groups does not allow any helical conformation even at lower pH and also even in a trifluoroethanol-water mixture (9∶1), suggesting that the branched hydroxyalkyl group is unfavorable for the formation of α-helix. Furthermore, the poly(N 5-di-2-hydroxyethyl-L-glutamine) is shown to have a rather disordered structure in the solid state.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 261 (1983), S. 340-345 
    ISSN: 1435-1536
    Schlagwort(e): reversed micelles ; sodium octanoate ; 1-hexanol ; 13C-NMR ; Na-NMR
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract The dynamic behavior of sodium octanoate (NaO), especially that of the polar headgroups of NaO, in1-hexanol in the presence of cosolubilized water was studied by Na-NMR and13C-NMR at 24 and 25 MHz. Na-NMR data have indicated that the mobility of the sodium ions of NaO shows the lowest value at 1.2 M of NaO at a given water content, which is related to the maximum amount of water cosolubilized into the system and the change in the structure of polar headgroups of NaO.13C-NMR data have shown that the mobility of methylene carbons, No. 5 and 6 of NaO, is higher than that of methylene carbons, No. 4 and 7, and that water molecules entered among the polar headgroups of NaO affect the mobility of methylene carbons of NaO, No. 5 and 6. The hydroxyl groups of1-hexanol were found to be contact with water molecules entered among the polar headgroups of NaO, and to fill the space among the hydrocarbon chains of NaO. By assuming spherical geometry the size of water pools and the average aggregation number were calculated, and the results were discussed on the basis of13C-NMR and Na-NMR data.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Colloid & polymer science 262 (1984), S. 61-66 
    ISSN: 1435-1536
    Schlagwort(e): Fourier transform infrared spectra ; FT-IR spectra ; micelle ; alkanesulfonates ; pentanesulfonate ; hexanesulfonate ; heptanesulfonate ; octanesulfonate ; premicellar aggregation ; counter-ion binding
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Maschinenbau
    Notizen: Abstract The concentration dependences of the Fourier transform infrared spectra of aqueous solutions of sodiumn-pentanesulfonate,n-hexanesulfonate,n-heptanesulfonate, andn-octanesulfonate were studied in concentration ranges encompassing the critical micellization concentrations (c.m.c). Changes in wavenumber, bandwidth, and intensity of infrared absorption bands were used to monitor the changes in molecular association with concentration. The premicellar aggregation below the c.m.c. may accompany the association of the alkyl chain, but not the counter-ion binding with the SO 3 − group. Above the c.m.c, the front location of the counter-ion against the SO 3 − group at the micelle surface is demonstrated.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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