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International Journal of Photoenergy
Volume 2009, Article ID 689450, 6 pages
http://dx.doi.org/10.1155/2009/689450
Research Article

Multifunctional Spirocyclic Systems

1Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don 344090, Russia
2Physical Engineering Department, Yanka Kupala State University, Grodno, 230023 Belorussia, Belarus
3Physical Department, V. Karazin Kharkiv National University, Kharkiv 61077, Ukraine
4Southern Scientific Center, Russian Academy of Sciences, Rostov-on-Don 344006, Russia
5Institute of Problems of Chemical Physics, Russian Academy of Science, Chernogolovka 142432, Russia

Received 26 March 2009; Revised 17 August 2009; Accepted 18 October 2009

Academic Editor: Mohamed Sabry Abdel-Mottaleb

Copyright © 2009 Boris Lukyanov et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. V. I. Minkin, “Photo-, thermo-, solvato-, and electrochromic spiroheterocyclic compounds,” Chemical Reviews, vol. 104, no. 5, pp. 2751–2776, 2004. View at Publisher · View at Google Scholar · View at PubMed · View at Scopus
  2. G. Favaro, G. Chidichimo, P. Formoso, S. Manfredi, U. Mazzucato, and A. Romani, “Chromatic and dynamic characteristics of some photochromes in the components of bifunctional photochromic and electro-optical devices,” Journal of Photochemistry and Photobiology A, vol. 140, no. 3, pp. 229–236, 2001. View at Google Scholar · View at Scopus
  3. M. Inouye, “Molecular crystals and liquid crystals science and technology. Section A: molecular crystals and liquid crystals,” Molecular Crystals and Liquid Crystals, vol. 246, pp. 169–172, 1994. View at Google Scholar
  4. M. A. Suzuki, T. Hashida, J. Hibino, and Y. Kishimoto, “Multiple optical memory using photochromic spiropyran aggregates,” Molecular Crystals and Liquid Crystals, vol. 246, pp. 389–396, 1994. View at Google Scholar
  5. Yu. S. Alekseenko, B. S. Lukyanov, A. N. Utenyshev et al., “Photo-and thermochromic spiranes. 24. Novel photochromic spiropyrans from 2,4-dihydroxyisophthalaldehyde,” Chemistry of Heterocyclic Compounds, vol. 42, no. 6, pp. 803–812, 2006. View at Publisher · View at Google Scholar · View at Scopus
  6. A. O. Bulanov, B. B. Safoklov, B. S. Luk'yanov et al., “Photochromic and thermochromic spiropyrans. 22. Spiropyrans of the 4-Oxo-3,4-dihydro-3H-1,3-benzoxazine series containing π-accepting substituents at position 8,” Chemistry of Heterocyclic Compounds, vol. 39, no. 3, pp. 315–317, 2003. View at Google Scholar
  7. M. B. Lukyanova, V. A. Kogan, and B. S. Lukyanov, “A new spiropyran with a cation receptor,” Chemistry of Heterocyclic Compounds, vol. 43, no. 11, pp. 1477–1478, 2007. View at Google Scholar
  8. B. S. Luk'yanov, L. E. Nivorozhkin, and V. I. Minkin, “Photo- and thermochromic spirans,” Chemistry of Heterocyclic Compounds, vol. 29, no. 2, pp. 152–154, 1993. View at Publisher · View at Google Scholar
  9. B. B. Safoklov, B. S. Luk'yanov, A. O. Bulanov et al., “Photo- [2H]chromene) possessing photochromic properties in the solid phase,” Russian Chemical Bulletin, vol. 51, no. 3, pp. 462–466, 2002. View at Google Scholar
  10. R. K. Chang and T. E. Furtak, Eds., Surface Enhanced Raman Scattering, Moscow, Russia, 1984, [Russian translation].
  11. K. Yoda, T. Ohzeki, T. Yuzawa, and H. Takahashi, “Resonance Raman studies of the solvatochromism and acid-base equilibria of 1,3,3-trimethylspiro-[2H-1-benzopyran-2,2-indoline],” Spectrochimica Acta, vol. 45A, no. 8, pp. 855–862, 1989. View at Google Scholar
  12. B. S. Luk'yanov, Yu. I. Ryabukhin, G. N. Dorofeenko, L. E. Nivorozhkin, and V. I. Minkin, “Photochromic and thermochromic spirans,” Chemistry of Heterocyclic Compounds, vol. 14, no. 2, pp. 122–127, 1978. View at Google Scholar