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Статья
2020

Synthesis and Acid–Base, Absorption, and Fluorescence Properties of Phthalocyanine Derivatives


Yu. B. IvanovaYu. B. Ivanova, O. A. DmitrievaO. A. Dmitrieva, Yu. V. KhrushkovaYu. V. Khrushkova, T. V. LyubimovaT. V. Lyubimova, A. S. SemeikinA. S. Semeikin, N. Zh. MamardashviliN. Zh. Mamardashvili
Российский журнал общей химии
https://doi.org/10.1134/S1070363220050151
Abstract / Full Text

Tetrakis{5,6-bis(4-tert-butylphenyl)pyrazino[2,3-c]}porphyrazine and tetra(4-tert-butyl)phthalocyanine have been synthesized, and their acid–base properties and electronic absorption and fluorescence spectra in acetonitrile and toluene at 298 and 295 K, respectively, have been studied. The synthesized compounds have been identified by electronic absorption and1H NMR spectroscopy and mass spectrometry. The effect of substituents in the molecular fragments of the macrocycle on the electronic and optical properties of the synthesized compounds has been estimated.

Author information
  • Krestov Institute of Solution Chemistry, Russian Academy of Sciences, 153045, Ivanovo, RussiaYu. B. Ivanova, O. A. Dmitrieva, T. V. Lyubimova & N. Zh. Mamardashvili
  • Ivanovo State University of Chemistry and Technology, 153460, Ivanovo, RussiaYu. V. Khrushkova, T. V. Lyubimova & A. S. Semeikin
References
  1. Berezin, B.D., Koordinatsionnye soedineniya porfirinov i ftalotsianina (Coordination Compounds of Porphyrins and Phthalocyanine), Moscow: Nauka, 1978.
  2. Stepanov, B.I., Vvedenie v khimiyu i tekhnologiyu organicheskikh krasitelei (Introduction to the Chemistry and Technology of Organic Dyes), Moscow: Khimiya, 1984.
  3. Porfiriny: spektroskopiya, elektrokhimiya, primenenie (Porphyrins: Spectroscopy, Electrochemistry, and Application), Enikolopyan, N.S., Ed., Moscow: Nauka, 1987.
  4. Stillman, M.J. and Nyokong, T., Phthalocyanines: Properties and Applications, Leznoff, C.C. and Lever, A.B.P., Eds., New York: VCH, 1989, vol. 1, p. 133.
  5. Liu, Z., Zhang, X., Zhang, Y., and Jiang, J., Spectrochim. Acta, Part A, 2007, vol. 67, no. 5, p. 1232. https://doi.org/10.1016/j.saa.2006.10.013
  6. Nonlinear Optics of Organic Molecules and Polymers, Nalwa, H.S. and Miyata, S., Eds., Boca Raton: CRC, 1997.
  7. Sheinin, V.B. and Ivanova, Yu.B., Russ. J. Phys. Chem. A, 2007, vol. 81, no. 8, p. 1250. https://doi.org/10.1134/S0036024407080134
  8. Petrov, O.A., Osipova, G.V., and Khelevina, O.G., Macroheterocycles, 2009, vol. 2, no. 2, p. 151.
  9. Bershtein, I.Ya. and Kaminskii, Yu.L., Spektrofotometricheskii analiz v organicheskoi khimii (Spectrophotometric Analysis in Organic Chemistry), Leningrad: Khimiya, 1986.
  10. Andrianov, V.G. and Malkova, O.V., Macroheterocycles, 2009, vol. 2, no. 2, p. 130.
  11. Hirao, H., J. Phys. Chem. A, 2011, vol. 115, no. 33, p. 9308. https://doi.org/10.1021/jp2052807
  12. Dhami, S., Mello, A.D., Rumbles, G., Bishop, S.M., Phillips, D., and Beeby, A., Photochem. Photobiol., 1995, vol. 61, no. 4, p. 341. https://doi.org/10.1111/j.1751-1097.1995.tb08619.x
  13. Whalley, M., J. Chem. Soc., 1961, p. 866. https://doi.org/10.1039/JR9610000866
  14. Lakowicz, J.R., Principles of Fluorescence Spectroscopy, New York: Springer, 2006, 3rd ed.
  15. Freyer, W., Mueller, S., and Teuchner, K.J., J. Photochem. Photobiol., C, 2004, vol. 163, nos. 1–2, p. 231. https://doi.org/10.1016/j.jphotochem.2003.12.003
  16. Vachova, L., Novakova, V., Kopecky, K., Miletin, M., and Zimcik, P., Dalton Trans., 2012, vol. 41, no. 38, p. 11651. https://doi.org/10.1039/c2dt31403g
  17. Karyakin, Yu.V. and Angelov, I.I., Chistye khimicheskie reaktivy (Pure Chemicals), Moscow: Khimiya, 1974, 4th ed.
  18. Ivanova, Yu.B., Churakhina, Yu.I., and Mamardashvili, N.Zh.,Russ. J. Gen. Chem., 2008, vol. 78, no. 4, p. 673. https://doi.org/10.1134/S1070363208100265
  19. Ivanova, Yu.B., Sheinin, V.B., and Mamardashvili, N.Zh., Russ. J. Gen. Chem., 2007, vol. 77, no. 8, p. 1458. https://doi.org/10.1134/S1070363207080270
  20. Ivanova, Yu.B. and Mamardashvili, N.Zh., J. Fluoresc., 2017, vol. 27, no. 5, p. 303. https://doi.org/10.1007/s10895-016-1958-1
  21. Ivanova, Yu.B., Mamardashvili, N.Zh., Semeikin, A.S., and Glazunov, A.V., Russ. J. Org. Chem., 2010, vol. 46, no. 6, p. 917. https://doi.org/10.1134/S1070428010060230
  22. Kruk, N.N., Starukhin, A.S., Mamardashvili, N.Zh., Sheinin, V.B., and Ivanova, Yu.B., RU Patent no. 2345352, 2009.
  23. Ivanova, Yu.B., Chizhova, N.V., Pukhovskaya, S.G., and Mamardashvili, N.Zh., Russ. J. Gen. Chem., 2014, vol. 84, no. 5, p. 939. https://doi.org/10.1134/S1070363214050260
  24. Nguyen, N.T., Mamardashvili, G.M., Kulikova, O.M., Scheblykin, I.G., Mamardashvili, N.Z., and Dehaen, W., RSC Adv., 2014, vol. 4, no. 38, p. 19703. https://doi.org/10.1039/C3RA45660A