Russian Journal of Organic Chemistry

, Volume 50, Issue 8, pp 1213–1217 | Cite as

New thiophene- and phenothiazine-containing chalcones: Synthesis, and electrochemical properties

  • D. G. Selivanova
  • E. V. Shklyaeva
  • T. V. Shavrina
  • G. G. Abashev
Short Communications

Keywords

Thiophene Chalcones Carbazole Phenothiazine Ethanone 

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References

  1. 1.
    Burroughes, J.H., Bradley, D.D.C., Brown, A.R., Marks, R.N., Mackey, K., Friend, R.H., Burn, P.L., and Holmes, A.B., Nature, 1990, vol. 347, p. 539.CrossRefGoogle Scholar
  2. 2.
    Zhang, Z., Fujiki, M., Tang, H., Motonaga, M., and Torimitsu, K., Macromolecules, 2002, vol. 35, p. 1988.CrossRefGoogle Scholar
  3. 3.
    Liu, B., Yu, W., Lai, Y., and Huang, W., Chem. Mater., 2001, vol. 13, p. 1984.CrossRefGoogle Scholar
  4. 4.
    Kong, X., Kulkarni, A.P., and Jenekhe, S.A., Macromolecules, 2003, vol. 36, p. 8992.CrossRefGoogle Scholar
  5. 5.
    Yang, L.Y., Wang, C., Li, L.Q., Janietz, S., Wedel, A., Hua, Y.L., and Yin, S.G., J. Polymer. Sci. A., 2007, vol. 45, p. 4291.Google Scholar
  6. 6.
    Syutkin, R.V., Abashev, G.G., Shklyaeva, E.V., and Kudryavtsev, P.G., Russ. J. Org. Chem., 2011, vol. 47, p. 530.CrossRefGoogle Scholar
  7. 7.
    Abashev, G., Sosnin, E., Shklyaeva, E., Ustalova, T., Osorgina, I., and Romanova, V., Phys. Status Solidi C, 2012, vol. 9, p. 1127.CrossRefGoogle Scholar
  8. 8.
    Sosnin, E.A., and Abashev, G.G., Izv. Vyssh. Uchebn. Zaved., Ser. khim. i khim. tekhnol., 2012, vol. 55, p. 80.Google Scholar
  9. 9.
    Agrinskaya, N.V., Lukoshkin, V.A., Kudryavtsev, V.V., Nosova, G.I., Sokolovskaya, N.A., and Yakimanskii, A.V., Phys. Solid State, 1999, vol. 41, p. 1914.CrossRefGoogle Scholar
  10. 10.
    Nelineinye Opticheskie Svoistva Organicheskikh Molekul i Crystallov, Shemla, D., and Ziss, Zh., Eds., Moscow: Mir, 1989.Google Scholar
  11. 11.
    Herbivo, C., Comel, A., Kirsch, G., and Raposo, M.M.M., Tetrahedron, 2009, vol. 65, p. 2079.CrossRefGoogle Scholar
  12. 12.
    Adams, R., and Noller, C.R., Org. Synth., 1925, vol. 5, p. 17.CrossRefGoogle Scholar
  13. 13.
    Su, W., Weng, Y., Jiang, L., Yang, Y., Zhao, L., Chen, Z., Li, Z., and Li, J., Org. Prep. Proc. Int., 2010, vol. 42, p. 503.CrossRefGoogle Scholar
  14. 14.
    Lilienkampf, A., Johansson, M.P., and Wähälä, K., Org. Lett., 2003, vol. 5, p. 3387.CrossRefGoogle Scholar
  15. 15.
    Meng, H., Zheng, J., Lovinger, A.J., Wang, B.-C., Van Patten, P.G., and Bao, Z., Chem. Mater., 2003, vol. 15, p. 1778.CrossRefGoogle Scholar
  16. 16.
    Jarowski, P.D., Wu, Y.-L., Boudon, C., Gisselbrecht, J.-P., Gross, M, Schweizer, W.B., and Diederich, F., Org. Biomol. Chem., 2009, vol. 7, p. 1312.CrossRefGoogle Scholar
  17. 17.
    Kirsch, G., Prim, D., Leising, F., and Mignani, G., J. Heterocyclic Chem., 1994, vol. 31, p. 1005.CrossRefGoogle Scholar
  18. 18.
    Shao, H., Chen, X., Wang, P., and Lu, Z., J. Lumin., 2007, vol. 127, p. 349.CrossRefGoogle Scholar

Copyright information

© Pleiades Publishing, Ltd. 2014

Authors and Affiliations

  • D. G. Selivanova
    • 1
    • 2
  • E. V. Shklyaeva
    • 2
    • 3
  • T. V. Shavrina
    • 3
  • G. G. Abashev
    • 1
    • 2
    • 3
  1. 1.Institute of Technical Chemistry, Ural BranchRussian Academy of SciencesPermRussia
  2. 2.Institute of Natural Sciences at Perm State Research UniversityPermRussia
  3. 3.Perm State Research UniversityPermRussia

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