Russian Journal of Organic Chemistry

, Volume 52, Issue 10, pp 1436–1439 | Cite as

Fluorescent chemosensors for mercury(II) cations

  • I. E. Tolpygin
  • K. S. Tikhomirova
  • Yu. V. Revinskii
  • A. D. Dubonosov
  • V. A. Bren’
  • V. I. Minkin
Article

Abstract

The condensation of 4,5-dimethoxy-2-(morpholin-4-yl)aniline with anthracene-9-carbaldehyde gave N-(anthracen-9-ylmethyl)-4,5-dimethoxy-2-(morpholin-4-yl)aniline, a selective and efficient fluorescent chemosensor for mercury(II) cations.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Chemosensors: Principles, Strategies, and Applications, Wang, B. and Anslyn, E.V., Eds., Hoboken, NJ Wiley, 2011.Google Scholar
  2. 2.
    Bren, V.A., Russ. Chem. Rev., 2001, vol. 70, p. 1017.CrossRefGoogle Scholar
  3. 3.
    Liu, Z., He, W., and Guo, Z., Chem. Soc. Rev., 2013, vol. 42, p. 1568.CrossRefGoogle Scholar
  4. 4.
    Kim, H.N., Ren, W.X., Kim, J.S., and Yoon, J., Chem. Soc. Rev., 2012, vol. 41, p. 3210.CrossRefGoogle Scholar
  5. 5.
    El-Safty, S.A. and Shenashen, M.A., Trends Anal. Chem., 2012, vol. 38, p. 98.CrossRefGoogle Scholar
  6. 6.
    Carter, K.P., Young, A.M., and Palmer, A.E., Chem. Rev., 2014, vol. 114, p. 4564.CrossRefGoogle Scholar
  7. 7.
    Saleem, M. and Lee, K.H., RSC Adv., 2015, vol. 5, p. 4926.CrossRefGoogle Scholar
  8. 8.
    Formica, M., Fusi, V., Giorgi, L., and Micheloni, M., Coord. Chem. Rev., 2012, vol. 256, p. 170.CrossRefGoogle Scholar
  9. 9.
    Kaur, N. and Kumar, S., Tetrahedron, 2011, vol. 67, p. 9233.CrossRefGoogle Scholar
  10. 10.
    Valeur, B. and Berberan-Santos, M.N., Molecular Fluorescence: Principles and Applications, Weinheim: Wiley-VCH, 2012, 2nd ed.CrossRefGoogle Scholar
  11. 11.
    Yu, L., Wang, S., Huang, K., Liu, Z., Gao, F., and Zeng, W., Tetrahedron, 2015, vol. 71, p. 4679.CrossRefGoogle Scholar
  12. 12.
    Wu, J., Liu, W., Ge, J., Zhang, H., and Wang, P., Chem. Soc. Rev., 2011, vol. 40, p. 3483.CrossRefGoogle Scholar
  13. 13.
    Tolpygin, I.E., Bren’, V.A., Dubonosov, A.D., Minkin, V.I., and Rybalkin, V.P., Russ. J. Org. Chem., 2003, vol. 39, p. 1364.CrossRefGoogle Scholar
  14. 14.
    Tolpygin, I.E., Rybalkin, V.P., Shepelenko, E.N., Popova, L.L., Revinskii, Yu.V., Tsukanov, A.V., Dmitrieva, O.I., Dubonosov, A.D., Bren’, V.A., and Minkin, V.I., Russ. J. Org. Chem., 2008, vol. 44, p. 557.CrossRefGoogle Scholar
  15. 15.
    Tolpygin, I.E., Shepelenko, E.N., Revinskii, Yu.V., Tsukanov, A.V., Dubonosov, A.D., Bren’, V.A., and Minkin, V.I., Russ. J. Org. Chem., 2009, vol. 45, p. 161.CrossRefGoogle Scholar
  16. 16.
    Tolpygin, I.E., Revinskii, Yu.V., Tsukanov, A.V., Dubonosov, A.D., Bren’, V.A., and Minkin, V.I., Russ. J. Org. Chem., 2011, vol. 47, p. 1305.CrossRefGoogle Scholar
  17. 17.
    Brown, N.M.D. and Nonhebel, D.C., Tetrahedron, 1968, vol. 24, p. 5655.CrossRefGoogle Scholar
  18. 18.
    Ehrlich, J. and Bogert, M.T., J. Org. Chem., 1947, vol. 12, p. 522.CrossRefGoogle Scholar
  19. 19.
    Stogryn, E.L., J. Med. Chem., 1970, vol. 13, p. 1106.CrossRefGoogle Scholar
  20. 20.
    Stogryn, E.L., J. Med. Chem., 1969, vol. 12, p. 185.CrossRefGoogle Scholar

Copyright information

© Pleiades Publishing, Ltd. 2016

Authors and Affiliations

  • I. E. Tolpygin
    • 1
  • K. S. Tikhomirova
    • 1
  • Yu. V. Revinskii
    • 2
  • A. D. Dubonosov
    • 2
  • V. A. Bren’
    • 1
  • V. I. Minkin
    • 1
    • 2
  1. 1.Institute of Physical and Organic ChemistrySouthern Federal UniversityRostov-on-DonRussia
  2. 2.Southern Scientific CenterRussian Academy of SciencesRostov-on-DonRussia

Personalised recommendations