Indolo[3,2-b]carbazole Derivatives Exhibiting Hole Conductivity in Organic Light-Emitting Diodes

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

A study is performed of the photophysical properties of indolo[3,2-b]carbazole-based compounds synthesized earlier. The charge carrier mobility in the space charge-limited current mode and the energy levels of the highest occupied and lowest unoccupied molecular orbitals in the compounds are determined. It is shown that indolo[3,2-b]carbazole derivatives can be used as hole transporting layers in organic light-emitting diodes.

About the authors

A. S. Steparuk

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia

N. A. Kazin

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia

S. G. Tolshchina

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia

R. A. Irgashev

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences; Ural Federal University

Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia; 620002, Yekaterinburg, Russia

E. F. Zhilina

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia

A. E. Aleksandrov

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
119071, Moscow, Russia

D. A. Lypenko

Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
119071, Moscow, Russia

I. R. Sayarov

National Research Nuclear University Moscow Engineering Physics Institute

Email: assteparuk@ios.uran.ru
115409, Moscow, Russia

A. R. Tameev

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences; Frumkin Institute of Physical Chemistry and Electrochemistry, Russian Academy of Sciences

Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia; 119071, Moscow, Russia

G. L. Rusinov

Postovsky Institute of Organic Synthesis, Ural Branch, Russian Academy of Sciences; Ural Federal University

Author for correspondence.
Email: assteparuk@ios.uran.ru
620137, Yekaterinburg, Russia; 620002, Yekaterinburg, Russia

References

  1. Lengvinaite S., Grazulevicius J.V., Grigalevicius S. et al. // Dyes Pigm. 2010. V. 85. P. 183. https://doi.org/10.1016/j.dyepig.2009.10.022
  2. Simokaitiene J., Stanislovaityte E., Grazulevicius J.V. et al. // J. Org. Chem. 2012. V. 77. P. 4924. https://doi.org/10.1021/jo202677j
  3. Stanislovaityte E., Simokaitiene J., Jankauskas V., Grazulevicius J.V. // Tetrahedron. 2014. V. 70. P. 6303. https://doi.org/10.1016/j.tet.2014.04.056
  4. Nan-Xing H., Shuang X., Zoran P. et al. // J. Am. Chem. Soc. – 1999. V. 121. P. 5097. https://doi.org/10.1021/ja9906554
  5. Zhao H.-P., Tao X.-T., Wang P. et al. // Org. Electron. 2007. V. 8. P. 673. https://doi.org/10.1016/j.orgel.2007.05.001
  6. Ting H.-C., Chen Y.-M., You H.-W. et al. // J. Mater. Chem. 2012. V. 22. P. 8399. https://doi.org/10.1039/C2JM30207A
  7. Shi H., Yuan J., Wu X. et al. // New J. Chem. 2014. V. 38. P. 2368. https://doi.org/10.1039/C4NJ00140K
  8. Li Y., Wu Y., Ong B.S. // Macromolecules. 2006. V. 39. P. 6521. https://doi.org/10.1021/ma0612069
  9. Boudreault P.-L.T., Wakim S., Blouin N. et al. // J. Am. Chem. Soc. 2007. V. 129. P. 9125. https://doi.org/10.1021/ja071923y
  10. Boudreault P.-L.T., Wakim S., Tang M.L. et al. // J. Mater. Chem. 2009. V. 19. P. 2921. https://doi.org/10.1039/B900271E
  11. Cai S.Y., Tian G.J., Li X. et al. // J. Mater. Chem. A. 2013. V. 1. P. 11295. https://doi.org/10.1039/C3TA11748K
  12. Qian X., Shao L., Li H. et al. // J. Power Sources. 2016. V. 319. P. 39. https://doi.org/10.1016/j.jpowsour.2016.04.043
  13. Yang H., Li Y. Yuling Z., Shupei Y. et al. // Dyes Pigm. 2021. V. 187. 109096. https://doi.org/10.1016/j.dyepig.2020.109096
  14. Светличный В.М., Александрова Е.Л., Мягкова Л.А. и др. // Физ. и техн. полупроводников. 2010. Т. 44. № 12. С. 1629. https://doi.org/10.1134/S1063782610120080
  15. Светличный В.М., Александрова Е.Л., Мягкова Л.А. и др. // Там же. 2011. Т. 45. № 10. С. 1392. https://doi.org/10.1134/S1063782611100204
  16. Dmitriyev A.V., Yusupov A.R., Irgashev R.A. et al. // Inorg. Mater. Appl. Res. 2017. V. 8. P. 172. https://doi.org/10.1134/S2075113317010105
  17. Степарук А.С., Толщина С.Г., Казин Н.А. и др. // Изв. АН, Сер. хим. 2021. № 6. С. 1109. https://doi.org/10.1007/s11172-021-3191-6
  18. Irgashev R.A., Kazin N.A., Rusinov G.L. et al. // Tet. Lett. 2017. V. 58. P. 3139. https://doi.org/10.1016/j.tetlet.2017.06.085
  19. Zhang Y., Ma Y., Kong L. et al. // Dyes Pigm. 2018. V. 159. P. 314. https://doi.org/10.1016/j.dyepig.2018.06.040
  20. Kühn M., Pflumm C., Glaser T. et al. // Org. Electron. 2017. V. 47. P. 79. https://doi.org/10.1016/j.orgel.2016.11.018
  21. Youn J.H., Baek S.J., Kim H.P. et al. // J. Mater. Chem. C. 2013. V. 1. P. 3250 https://doi.org/10.1039/C3TC00855J

Supplementary files

Supplementary Files
Action
1. JATS XML
2.

Download (87KB)
3.

Download (132KB)
4.

Download (95KB)
5.

Download (30KB)
6.

Download (43KB)
7.

Download (50KB)
8.

Download (73KB)
9.

Download (29KB)
10.

Download (89KB)
11.

Download (89KB)
12.

Download (101KB)

Copyright (c) 2023 А.С. Степарук, Н.А. Казин, С.Г. Толщина, Р.А. Иргашев, Е.Ф. Жилина, А.Е. Александров, Д.А. Лыпенко, И.Р. Саяров, А.Р. Тамеев, Г.Л. Русинов

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies