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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 1073-1080 
    ISSN: 0887-6266
    Keywords: Nylon-11 ; infrared spectroscopy ; Fermi resonance ; crystal structures ; symmetry ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Nylon-11 is prepared by casting from the solvents trifluoroacetic acid and m-cresol and by melt-crystallization. Room-temperature infrared spectra are compared in terms of possible crystal structures. The spectra are examined for the presence of Fermi resonance which occurs between the N-H stretching fundamental mode and the overtone and combination modes of the amide I and II vibrations. An analysis of peak frequencies and intensities is used to provide support for the assignment of the amide II overtone and the amide I + II combination modes. A newly observed peak in the spectra is assigned to the amide I overtone. Symmetry considerations are discussed which predict the resonance of the overtone and combination modes with the N-H stretching fundamental. © 1992 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 34 (1996), S. 781-788 
    ISSN: 0887-6266
    Keywords: nylon ; infrared spectroscopy ; electric field poling ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dipole reorientation under the influence of an electric field is investigated in oriented nylon 11 films with polarized infrared spectroscopy for the amide A and amide I bands. Butterfly-shaped hysteresis loops are obtained from peak intensity versus applied electric field strength. Least-squares Gaussian curve fitting of the resolved multiple contributions to the amide I peak show that the components change in either a continuously reducing S-shaped fashion, or in butterfly-shaped curves under ac poling fields. Time-dependent studies of the absorption intensities show that both ordered and disordered species switch towards the electric field direction with the application of electric fields higher than the coercive field. Upon field removal, only the disordered species show orientation relaxation away from the field direction. Below the coercive field, neither species responds orientationally to the field. © 1996 John Wiley & Sons, Inc.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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