Russian Journal of General Chemistry

, Volume 83, Issue 11, pp 2075–2083

Synthesis, structure, and spectral luminescent properties of novel 1,2,4-triazole derivatives containing benzthiazole group

  • A. D. Beldovskaya
  • G. A. Dushenko
  • N. I. Vikrishchuk
  • L. D. Popov
  • Yu. V. Revinskii
  • I. E. Mikhailov
Article

Abstract

Novel derivatives of 1,2,4-triazol with benzthiazole fragment have been prepared, including Cu(II) and Be complexes. Their structure and spectral luminescent properties have been investigated. With ohydroxyphenylbenzthiazolyl-1,2,4-triazole as an example, the density functional theory has been applied to find the stable conformers with different structures of coordination nodes, stabilized by intramolecular hydrogen bonds between hydroxyl group hydrogen and either triazole of benzthiazole nitrogen.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Al-Masoudi, I.A., Al-Soud, Y.A., Al-Salihi, N.J., and Al-Masoudi, N.A., Chem. Heterocycl. Comp., 2006, no. 11, p. 1377.Google Scholar
  2. 2.
    Tkisler, A., Usunanali, E., and Demirbas, A., Ind. J. Pharm. Sci., 2000, no. 62, p. 371.Google Scholar
  3. 3.
    Toraskar, M.P., Kadam, V. J., and Kulkarni V.M., Int. J. Pharm. Sci., 2010, vol. 2, no. 2, p. 132.Google Scholar
  4. 4.
    Parmar, K., Suthar, B., Prajapati, S., and Sanduthar, A., J. Heterocycl. Chem., 2010, vol. 47, no. 1, p. 156.Google Scholar
  5. 5.
    Haasnoot, J.G., Coord. Chem. Rev., 2000, vols. 200–202, p. 131.CrossRefGoogle Scholar
  6. 6.
    Lavrenova, L.G., Ikorskiim V.N., Sheludyakova, L.A., Naumov, D.Yu., and Boguslavskii, E.G., Russ. J. Coord. Chem., 2004, vol. 30, no. 6, p. 413.CrossRefGoogle Scholar
  7. 7.
    Dorofeenko, G.N., Ryabukhin, Yu.I., Bulgarevich, S.B., Mezheritskii, V.V., and Ryabukhina, O.Yu., Zh. Org. Khim., 1977, vol. 13, no. 11, p. 2459.Google Scholar
  8. 8.
    Ryabukhin, Yu.I., Faleeva, L.N., Gorbunova, M.O., Kovaleva, T.V., Uflyand, I.E., and Sheinker, V.N., Zh. Org. Khim., 1988, vol. 24, no. 9, p. 599.Google Scholar
  9. 9.
    Shasheva, E.Yu., Vikrishchuk, N.I., Popov, L.D., Kletskii, M.E., Antipin, M.Yu., Vikrishchuk, A.D., and Mikhailov, I.E., Russ. J. Gen. Chem., 2009, vol. 79, no. 10, p. 2234.CrossRefGoogle Scholar
  10. 10.
    Shasheva, E.Yu., Vikrishchuk, N.I., Popov, L.D., Minkin, V.I., Kletskii, M.E., Antipin, M.Yu., Vikrishchuk, A.D., and Mikhailov, I.E., Russ. J. Org. Chem., 2010, vol. 46, no. 7, p. 1079.CrossRefGoogle Scholar
  11. 11.
    Vikrishchuk, A.D., Popov, L.D., Vikrishchuk, N.I., Morozov, P.G., and Mikhailov, I.E., Russ. J. Gen. Chem., 2011, vol. 81, no. 1, p. 132.CrossRefGoogle Scholar
  12. 12.
    Ryabukhin, Yu.I., Shibaeva, N.V., Kuzharov, A.S., Korobkova, V.G., Khokhlov, A.V., and Garnovskii, A.D., Koord. Khim., 1987, vol. 12, no. 7, p. 869.Google Scholar
  13. 13.
    Antsyshkina, A.S., Porai-Kashits, M.A., Garnovskii, D.A., Faleeva, L.N., Ryabukhin, Yu.I., and Garnovskii, A.D., Koord. Khim., 1990, vol. 16, no. 12, p.Google Scholar
  14. 14.
    Hage, R., Haasnoot, J.G., Wang, R., Ryan, E.M., Vos, J.G., Spec, A.L., and Duisenberg, J.M., Inorg. Chim. Acta, 1990, vol. 174, p. 77.CrossRefGoogle Scholar
  15. 15.
    Steinhauser, S., Heinz, U., Bartholoma, M., Weyhermuller, T., Nick, H., and Hegetschweiler, K., Eur. J. Inorg. Chem., 2004, no. 22, p. 4177.Google Scholar
  16. 16.
    Keyes, T.E., Evrard, B., Vos, J.G., Johannes, G., Brady, C., McGarvey, J.J., and Jayaweera, P., Dalton Trans., 2004, vol. 15, p. 2341.CrossRefGoogle Scholar
  17. 17.
    Dushenko, G.A, Vikrishchuk, A.D., Mikhailov, I.E., Vikrishchuk, N.I., Vestn. YuNTs, 2013, vol. 9, no 1, p. 37.Google Scholar
  18. 18.
    Kotilevskii, S.I., Pedash, Yu.F., Verezubova, A.A., Ptyagina, L.M., and Doroshenko, A.O., Vestn. Kharkov. Univ., 1999, vol. 454, no. 4(27), p. 130.Google Scholar
  19. 19.
    Kulkarni, A.P., Tonzola, Ch.J., Babel, A., and Jenekhe, S.A., Chem. Mater., 2004, vol. 16, p. 4556.CrossRefGoogle Scholar
  20. 20.
    Bettencourt-Dias, A., Dalton Trans., 2007, no. 22, p. 2229.Google Scholar
  21. 21.
    Mikhailov, I.E., Dushenko, G.A., Starikov, D.A., Mikhailova, O.I., and Minkin, V.I., Vestn. YuNTs, 2010, vol. 6, no 4, p. 32.Google Scholar
  22. 22.
    Arduini, M., Felluga, F., Mancin, F., Rossi, P., Tecilla, P., Tonellato, U., and Valentinuzzi, N., Chem. Commun., 2003, p. 1606.Google Scholar
  23. 23.
    Heinz, U., Hegetschweiler, K., Acklin, P., Faller, B., Lattmann, R., and Schnebli, H.P., Angew. Chem. Int. Ed., 1999, vol. 38, p. 2568.CrossRefGoogle Scholar
  24. 24.
    Ryabukhin, Yu.I., Mezheritskii, V.V., and Dorofeenko, G.N., Zh. Obshch. Khim., 1974, vol. 44, no. 12, p. 2792.Google Scholar
  25. 25.
    Doroshenko, A.O., Posokhov, E.A., Verezubova, A.A., and Ptyagina, L.M., J. Phys. Org. Chem., 2000, vol. 13, p. 253.CrossRefGoogle Scholar
  26. 26.
    Kotelevskiy, S.I., J. Lumin., 1998, vol. 79, no. 3, p. 211.CrossRefGoogle Scholar
  27. 27.
    Weissberger, A., Riddick, J.A.., Toops, E.E. and Proskauer, E., Organic Solvents: Physical Constants and Methods of Purification, Interscience Publishers, 1935.Google Scholar
  28. 28.
    Foresman, J.B. and Frisch, E., Exploring Chemistry with Electronic Structure Methods, Pittsburg: Gaussian Inc., 1996.Google Scholar

Copyright information

© Pleiades Publishing, Ltd. 2013

Authors and Affiliations

  • A. D. Beldovskaya
    • 1
  • G. A. Dushenko
    • 2
    • 3
  • N. I. Vikrishchuk
    • 4
  • L. D. Popov
    • 4
  • Yu. V. Revinskii
    • 2
  • I. E. Mikhailov
    • 2
    • 4
  1. 1.Institute of Arid Zones, Southern Scientific CenterRussian Academy of SciencesRostov-on-DonRussia
  2. 2.Southern Scientific CenterRussian Academy of SciencesRostov-on-DonRussia
  3. 3.Research Institute of Physical and Organic ChemistrySouthern Federal UniversityRostov-on-DonRussia
  4. 4.Southern Federal UniversityRostov-on-DonRussia

Personalised recommendations