New 5,6-Difl uoro- and 5,6-Dicyano Containing 2,1,3-Benzothiadiazoles of the Donor-Acceptor Type: Synthesis, Photophysical and Electroluminescent Properties
- Авторлар: 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
-
Мекемелер:
- A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
- Шығарылым: Том 122, № 2 (2024): THEMED SECTION: FUNDAMENTAL PRINCIPLES OF ORGANIC ELECTROCHEMISTRY, CREATION OF NEW FUNCTIONAL MATERIALS AND MATERIALS FOR MEDICINE
- Беттер: 18-29
- Бөлім: THEMED SECTION: FUNDAMENTAL SCIENTIFIC RESEARCH IN THE FIELD OF NATURAL SCIENCES
- URL: https://bakhtiniada.ru/1605-8070/article/view/303409
- DOI: https://doi.org/10.22204/2410-4639-2024-122-02-18-29
- ID: 303409
Дәйексөз келтіру
Толық мәтін
Аннотация
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.
Негізгі сөздер
Авторлар туралы
Pavel Gribanov
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Хат алмасуға жауапты Автор.
Email: gribanovps@mail.ru
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Anna Philippova
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: anyfil96@gmail.com
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Daria Vorobyeva
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: vorobyeva-daria@yandex.ru
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Sergey Tokarev
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: tokarev@ineos.ac.ru
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Dmitry Lypenko
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: dalypenko@gmail.com
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Artem Dmitriev
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: oleduff@mail.ru
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Dmitry Loginov
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: dloginov@ineos.ac.ru
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Sergey Osipov
A.N. Nesmeyanov Institute of Organoelement Compounds, RAS
Email: osipov@ineos.ac.ru
Ресей, 28-1 Vavilov Str., Moscow, 119334, Russia
Әдебиет тізімі
- 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.
Қосымша файлдар
