Polymer Science Series B

, Volume 52, Issue 7–8, pp 391–396 | Cite as

Branched polyphenylquinoxalines containing naphthoxazine-5,8-disulfonic acid groups

  • A. L. Rusanov
  • E. A. Solodova
  • E. G. Bulycheva
  • N. M. Belomoina


Branched carboxylated polyphenylquinoxalines are prepared via the interaction of tris(α-diketone), 4,4′-bis(phenylglyoxalyl)benzyl, with an equimolar amount of 3,4-diaminobenzoic acid and subsequent interaction of the reaction product with an equimolar amount of bis(o-phenylenediamines). Polymeranalogous transformations of these polymers with 1-amino-8-naphthol-3,6-disulfonic acid sodium salt monohydrate in Eaton’s reagent yield earlier undescribed branched polyphenylquinoxalines containing side naphthoxazine-5,8-disulfonic acid groups.


Polymer Science Series Disulfonic Acid Polymer Analogous Transformation Acid Monosodium Salt Acid Side Group 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.


  1. 1.
    J. C. Lasseques, in Proton Conductors: Solids, Membranes and Gels, Ed. by P. Colombon (Cambridge Univ. Press, Cambridge, 1992), p. 311.CrossRefGoogle Scholar
  2. 2.
    S. Watkins, in Fuel Cell Systems, Ed. by L. G. Blumen and M. M. Mugerwa (Plenum, New York, 1993).Google Scholar
  3. 3.
    T. A. Zawodzinski, C. Deraum, S. Rodzinski, et al., J. Electrochem. Soc. 140, 1041 (1993).CrossRefGoogle Scholar
  4. 4.
    O. J. Savadogo, New Mater. Electrochem. Syst. 1, 66 (1998).Google Scholar
  5. 5.
    M. Rikukawa and K. Sanui, Prog. Polym. Sci. 25, 1463 (2000).CrossRefGoogle Scholar
  6. 6.
    J. A. Kerres, J. Membr. Sci. 185, 3 (2001).CrossRefGoogle Scholar
  7. 7.
    A. L. Rusanov, D. Yu. Likhachev, and K. Müellen, Usp. Khim. 71, 862 (2002).Google Scholar
  8. 8.
    A. L. Rusanov, D. Yu. Likhatchev, P. V. Kostoglodov, et al., Adv. Polym. Sci. 179, 83 (2005).Google Scholar
  9. 9.
    M. A. Hickner, H. Ghassemi, Y. S. Kim, et al., Chem. Rev. 104, 4587 (2004).CrossRefGoogle Scholar
  10. 10.
    P. Jannasch, Curr. Opin. Colloid Interface Sci. 8, 96 (2003).CrossRefGoogle Scholar
  11. 11.
    A. L. Rusanov, E. A. Solodova, E. G. Bulycheva, et al., Usp. Khim. 76, 1073 (2007).Google Scholar
  12. 12.
    L. J. Bellamy, The Infrared Spectra of Complex Molecules (Methuen, London, 1957; Inostrannaya Literatura, Moscow, 1963).Google Scholar
  13. 13.
    M. L. Keshtov, Doctoral Dissertation in Chemistry (Moscow, 2001).Google Scholar
  14. 14.
    M. S. Yusubov, V. D. Filimonov, I. V. Khlebnikov, et al., Zh. Org. Khim. 29, 1843 (1993).Google Scholar

Copyright information

© Pleiades Publishing, Ltd. 2010

Authors and Affiliations

  • A. L. Rusanov
    • 1
  • E. A. Solodova
    • 1
  • E. G. Bulycheva
    • 1
  • N. M. Belomoina
    • 1
  1. 1.Nesmeyanov Institute of Organoelement CompoundsRussian Academy of SciencesMoscowRussia

Personalised recommendations