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  • 1995-1999  (1)
  • 1965-1969  (1)
  • Chemistry  (2)
  • Molecular structure
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  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 33 (1995), S. 803-811 
    ISSN: 0749-1581
    Keywords: NMR ; 13C NMR ; 2D INADEQUATE ; polycyclic benzenoid aromatics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A computerized analysis of a single 2D INADEQUATE spectra assigns all of the 13C chemical shifts in fairly complex aromatic systems. Without the aid of the computer this information is often difficult, if not impossible, to retrieve owing to overlap of the signals in the double quantum dimension. In addition, the use of the computerized analysis allows for the interpretation of INADEQUATE spectra with much lower signal-to-noise ratios than are practical if the analysis were to be done visually. Finally, narrowing the spectral window to a subset of the entire spectrum and the companion advantages are demonstrated. The assignments of the aromatic chemical shifts in 2-methoxydibenzofuran, 6-methylchrysene, 1-decylpyrene, and 7-methylbenzo[a]pyrene illustrate the power of automated pattern recognition methods while supplying previously unavailable chemical shift assignments on these complex fused polycyclic aromatic systems.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Proton magnetic resonance spectra were obtained for a number of representative phenol-formaldehyde dimers and trimers of known structure and for related compounds having methyl or chloro substituents on the aromatic ring. The data thus obtained, particularly for the methylene protons, were used in the interpretation of the structure of well characterized, linear phenol-formaldehyde polymers and the corresponding halogenated polymers prepared by the condensation of o- and p-chlorophenol with formaldehyde. In all cases there was a shift to lower field as the methylene linkage was varied from para-para to ortho-para to ortho-ortho, although in certain instances the ortho-para and ortho-ortho peaks moved very close together. The spectra obtained indicated that the condensation of o-chlorophenol with formaldehyde proceeds in an essentially random manner, since the ratio of ortho-ortho to ortho-para to para-para methylene linkages was found to be 1:2:1, within the limits of experimental error. The preliminary results obtained in this work clearly demonstrate the potential utility of PMR as a valuable tool in the characterization of the highly complex products obtained from phenol-formaldehyde systems.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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