Photophysical and Photochemical Properties of Perylene–(Cyanine Dye) Dyad in the VIS–NIR Spectrum Region

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Abstract

The photophysical properties of an original covalently-bonded dyad based on a perylene derivative and IR-780 cyanine dye were studied. The dyad has pronounced absorption in the NIR region of the spectrum and a strong fluorescence signal, which is weakly quenched by the influence of the perylene derivative. Upon excitation of the dyad in the absorption region of perylene, a fluorescence signal from IR-780 is detected due to the Förster energy transfer mechanism. It is shown that the dyad does not generate singlet oxygen upon photoexcitation in the NIR region of the spectrum. However, it can generate superoxide anion radicals, indicating the presence of the photoinduced electrons transfer from the dye to the perylene.

About the authors

A. V. Kozlov

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences

Email: lexsetlex@gmail.com
Chernogolovka, Russia

L. R. Sizov

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences

Email: lexsetlex@gmail.com
Chernogolovka, Russia

D. V. Revina

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences; Moscow State University

Email: lexsetlex@gmail.com
Chernogolovka, Russia; 119991, Moscow, Russia

A. Yu. Rybkin

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences

Email: lexsetlex@gmail.com
Chernogolovka, Russia

N. S. Goryachev

Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences; Moscow State University

Author for correspondence.
Email: lexsetlex@gmail.com
Chernogolovka, Russia; 119991, Moscow, Russia

References

  1. Chen H., Zhang W., Zhu G. et al. // Nat. Rev. Mater. 2017. V. 2. № 7. P. 17024. https://doi.org/10.1038/natrevmats.2017.24
  2. Yang Z., Tian R., Wu J. et al. // ACS Nano 2017. V. 11. № 4. P. 4247. https://doi.org/10.1021/acsnano.7b01261
  3. Li J., Pu K. // Chem. Soc. Rev. 2019. V. 48. № 1. P. 38. https://doi.org/10.1039/C8CS00001H
  4. Wang Y.-Y.Y., Liu Y.-C.C., Sun H. et al. // Coord. Chem. Rev. 2019. V. 395. P. 46. https://doi.org/10.1016/j.ccr.2019.05.016
  5. Meredith P., Li W., Armin A. // Adv. Energy Mater. 2020. V. 10. № 33. P. 2001788. https://doi.org/10.1002/aenm.202001788
  6. Praikaew P., Maniam S., Charoenpanich A. et al. // J. Photochem. Photobiol. A Chem. 2019. V. 382. P. 111852. https://doi.org/10.1016/j.jphotochem.2019.05
  7. Fan Q., Cheng K., Yang Z. et al. // Adv. Mater. 2015. V. 27. № 5. P. 843. https://doi.org/10.1002/adma.201402972
  8. Yang Z., Dai Y., Shan L. et al. // Nanoscale Horizons 2019. V. 4. № 2. P. 426. https://doi.org/10.1039/C8NH00307F
  9. Li Q., Huang C., Liu L. et al. // Cytom. Part A 2018. № 93. P. 997. https://doi.org/10.1002/cyto.a.23596
  10. Rybkin A.Y., Belik A.Y., Goryachev N.S. et al. // Dye. Pigment. 2020. V. 180. P. 108411. https://doi.org/10.1016/j.dyepig.2020.108411
  11. Rybkin A.Y., Belik A.Y., Kraevaya O.A. et al. // Dye. Pigment. 2019. V. 160. P. 457. https://doi.org/10.1016/j.dyepig.2018.06.041
  12. Spiller W., Kliesch H., Wöhrle D. et al. // J. Porphyrins Phthalocyanines 1998. V. 02. № 02. P. 145. https://doi.org/10.1002/(SICI)1099-1409(199803/04)2:2<145::AID-JPP60>3
  13. Kuznetsova N.A., Gretsova N.S., Derkacheva V.M. et al. // Russ. J. Gen. Chem. 2002. V. 72. № 2. P. 300. https://doi.org/10.1023/A:1015402524813
  14. Yamakoshi Y., Umezawa N., Ryu A. et al. // J. Am. Chem. Soc. 2003. V. 125. № 42. P. 12803. https://doi.org/10.1021/ja0355574
  15. Ford W.E., Kamat P. V. // J. Phys. Chem. 1987. V. 91. № 25. P. 6373. https://doi.org/10.1021/j100309a012
  16. Levitz A., Marmarchi F., Henary M. // Molecules. 2018. V. 23. № 2. P. 1. 10.3390/molecules23020226
  17. Rurack K. // Stand. Qual. Assur. Fluoresc. Meas. I Springer Berlin Heidelberg, 2008 P. 101. https://doi.org/10.1007/4243_2008_019
  18. Seybold P.G., Gouterman M., Callis J. // Photochem. Photobiol. 1969. V. 9. № 3. P. 229. https://doi.org/10.1111/j.1751-1097.1969.tb07287.x
  19. Müller S., Mantareva V., Stoichkova N. et al. // J. Photochem. Photobiol. B Biol. 1996. V. 35. № 3. P. 167. https://doi.org/10.1016/S1011-1344(96)07294-6
  20. Rybkin A.Y., Belik A.Y., Tarakanov P.A. et al. // Macroheterocycles. 2019. V. 12. № 2. P. 181. https://doi.org/10.6060/mhc190446r

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Copyright (c) 2023 А.В. Козлов, Л.Р. Сизов, Д.В. Ревина, А.Ю. Рыбкин, Н.С. Горячев

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