New 5,6-Difl uoro- and 5,6-Dicyano Containing 2,1,3-Benzothiadiazoles of the Donor-Acceptor Type: Synthesis, Photophysical and Electroluminescent Properties
- Authors: Gribanov P.S.1, Philippova A.N.1, Vorobyeva D.V.1, Tokarev S.D.1, Lypenko D.A.1, Dmitriev A.V.1, Loginov D.A.1, Osipov S.N.1
-
Affiliations:
- A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
- Issue: Vol 122, No 2 (2024): THEMED SECTION: FUNDAMENTAL PRINCIPLES OF ORGANIC ELECTROCHEMISTRY, CREATION OF NEW FUNCTIONAL MATERIALS AND MATERIALS FOR MEDICINE
- Pages: 18-29
- Section: THEMED SECTION: FUNDAMENTAL SCIENTIFIC RESEARCH IN THE FIELD OF NATURAL SCIENCES
- URL: https://journal-vniispk.ru/1605-8070/article/view/303409
- DOI: https://doi.org/10.22204/2410-4639-2024-122-02-18-29
- ID: 303409
Cite item
Full Text
Abstract
An effective synthetic approach to new 5,6-difluoro- and 5,6-dicyano-containing 2,1,3-benzothiadiazoles (BTDs) of the donor-acceptor (D-A) type has been developed, the assembly method of which is based on palladiumcatalyzed cross-coupling reactions. An initial study of the photophysical properties of the compounds obtained was performed. A trial series of organic light-emitting diodes (OLED) with different contents of synthesized D-π-A-π-D triads in the light-emitting layer was made and their electroluminescent (EL) characteristics were studied as well.
About the authors
Pavel S. Gribanov
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Author for correspondence.
Email: gribanovps@mail.ru
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Anna N. Philippova
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: anyfil96@gmail.com
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Daria V. Vorobyeva
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: vorobyeva-daria@yandex.ru
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Sergey D. Tokarev
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: tokarev@ineos.ac.ru
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Dmitry A. Lypenko
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: dalypenko@gmail.com
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Artem V. Dmitriev
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: oleduff@mail.ru
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Dmitry A. Loginov
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: dloginov@ineos.ac.ru
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
Sergey N. Osipov
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: osipov@ineos.ac.ru
Russian Federation, 28-1 Vavilov Str., Moscow, 119334, Russia
References
- S.H. Park, A. Roy, S. Beaupré, S. Cho, N. Coates, J.S. Moon, D. Moses, M. Leclerc, K. Lee, A.J. Heeger Nat. Photonics, 2009, 3, 297. doi: 10.1038/nphoton.2009.69.
- J.E. Anthony Angew. Chem. Int. Ed., 2008, 47(3), 452. doi: 10.1002/anie.200604045.
- M.D. Watson, A. Fechtenkotter, K. Mullen Chem. Rev., 2001, 101(5), 1267. doi: 10.1021/cr990322p.
- U. Mitschke, P. Bäuerle J. Mater. Chem., 2000, 10(7), 1471. doi: 10.1039/a908713c.
- F. Ni, Z. Wu, Z. Zhu, T. Chen, K. Wu, C. Zhong, K. An, D. Wei, D. Ma, C. Yang J. Mater. Chem. C, 2017, 5(6), 1363. doi: 10.1039/c7tc00025a.
- Y. Rout, Y. Jang, H.B. Gobeze, R. Misra, F. D’Souza J. Phys. Chem. C, 2019, 123(38), 23382. doi: 10.1021/acs.jpcc.9b06632.
- L.S. Cui, H. Nomura, Y. Geng, J.U. Kim, H. Nakanotani, C. Adachi Angew. Chem. Int. Ed., 2017, 56(6), 1571. doi: 10.1002/anie.201609459.
- M. Ke, X. Tan, Y. Wang, B. Li, X. Zeng, X. Miao, X. Cheng, W. Deng J. Phys. Chem. C, 2021, 125(35), 19325. doi: 10.1021/acs.jpcc.1c06012.
- J. Kumsampao, C. Chaiwai, P. Chasing, T. Chawanpunyawat, S Namuangruk, T. Sudyoadsuk, V. Promarak Chem. Asian J., 2020, 15(19), 3029. doi: 10.1002/asia.202000727.
- P.S. Gribanov, D.A. Lypenko, A.V. Dmitriev, S.I. Pozin, M.A. Topchiy, A.F. Asachenko, D.A. Loginov, S.N. Osipov Mendeleev Commun., 2021, 31(1), 33. doi: 10.1016/j.mencom.2021.01.009.
- P.S. Gribanov, D.A. Loginov, D.A. Lypenko, A.V. Dmitriev, S.I. Pozin, A.E. Aleksandrov, A.R. Tameev, I.L. Martynov, A.Y. Chernyadyev, S.N. Osipov Molecules, 2021, 26(24), 7596. doi: 10.3390/molecules26247596.
- P.S. Gribanov, D.A. Loginov, D.A. Lypenko, A.V. Dmitriev, S.D. Tokarev, A.E. Aleksandrov, A.R. Tameev, A.Y. Chernyadyev, S.N. Osipov Mendeleev Commun., 2023, 33(5), 701. doi: 10.1016/j.mencom.2023.09.035.
- P.S. Gribanov, D.V. Vorobyeva, S.D. Tokarev, D.A. Petropavlovskikh, D.A. Loginov, S.E. Nefedov, F.M. Dolgushin, S.N. Osipov Eur. J. Org. Chem., 2022, 2022(13), e202101572. doi: 10.1002/ejoc.202101572.
- P.S. Gribanov, D.V. Vorobyeva, S.D. Tokarev, D.A. Loginov, A.A. Danshina, S.M. Masoud, S.N. Osipov Asian J. Org. Chem., 2022, 11(12), e202200603. doi: 10.1002/ajoc.202200603.
- J. Pommerehne, H. Vestweber, W. Guss, R.F. Mahrt, H. Bässler, M. Porsch J. Daub. Adv. Mater., 2004, 7(6), 551. doi: 10.1002/adma.19950070608.
- R.N. Bennett, A.D. Hendsbee, J.H.L. Ngai, A. Ganguly, Y. Li, T.L. Kelly ACS Appl. Electron. Mater., 2020, 2(7), 2039. doi: 10.1021/acsaelm.0c00305.
- A.R. Davalos, E. Sylvester, S.T. Diver Organometallics, 2019, 38(11), 2338. doi: 10.1021/acs.organomet.9b00152.
- N. Niu, Y. Yu, Z. Zhang, M. Kang, L. Wang, Z. Zhao, D. Wang, B.Z. Tang Chem. Sci., 2022, 13(20), 5929. doi: 10.1039/d2sc01260j.
Supplementary files
