Theoretical and Experimental Chemistry

, Volume 19, Issue 2, pp 224–228 | Cite as

Recognition of isomers in a series of derivatives of sulforhodamine S by 13C-NMR spectroscopy

  • Yu. S. Ryabokobylko
  • N. V. Abrosimova
  • I. A. Krasavin
  • G. M. Adamova
  • B. N. Parusnikov
  • I. L. Parbuzina
  • V. A. Inshakova
Brief Communications
  • 17 Downloads

Keywords

Spectroscopy Sulforhodamine 

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Literature cited

  1. 1.
    B. Stothers, Carbon-13 nmp Spectroscopy, Acad. Press, New York (1972).Google Scholar
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    I. S. Ioffe and E. I. Zhukova, “Rhodamine sulfofluoride,” Zh. Obshch. Khim., 34, No. 10, 3510 (1964).Google Scholar
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    T. Shaefer and W. J. E. Parr, “Long-range 1H-19F spin-spin coupling constants in benzene-sulfonyl fluoride and some of its derivatives. Insensitivity of 19F shifts to ortho-substituents,” Can. J. Chem., 56, No. 13, 1717–1720 (1978).Google Scholar
  4. 4.
    L. F. Johnson and W. C. Jankowski, Carbon-13 NMR Spectra. A Collection of Assigned, Coded, and Indexed Spectra, Wiley-Interscience, New York (1972).Google Scholar
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    L. Ernst, V. Wray, V. A. Chertkow, and N. M. Sergeyev, “High resolution proton-coupled 13C NMR spectra of monosubstituted benzenes. Theoretical and empirical correlations of JCH,” J. Magn. Reson., 25, No. 1, 123–139 (1977).Google Scholar
  6. 6.
    O. Exner, “Characteristic vibrations of the sulfonyl group,” Collect. Czech. Chem. Commun., 78, No. 4, 380–387 (1974).Google Scholar

Copyright information

© Plenum Publishing Corporation 1983

Authors and Affiliations

  • Yu. S. Ryabokobylko
    • 1
  • N. V. Abrosimova
    • 1
  • I. A. Krasavin
    • 1
  • G. M. Adamova
    • 1
  • B. N. Parusnikov
    • 1
  • I. L. Parbuzina
    • 1
  • V. A. Inshakova
    • 1
  1. 1.All-Union Scientific-Research Institute of Chemical Reagents and Ultrapure Chemical SubstancesMoscow

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