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Название: Dibenzo[ f,h]furazano[3,4- b]quinoxalines: Synthesis by Intramolecular Cyclization through Direct Transition Metal-Free C-H Functionalization and Electrochemical, Photophysical, and Charge Mobility Characterization
Авторы: Kvashnin, Y. A.
Verbitskiy, E. V.
Eltsov, O. S.
Slepukhin, P. A.
Tameev, A. R.
Nekrasova, N. V.
Rusinov, G. L.
Nunzi, J. -M.
Chupakhin, O. N.
Charushin, V. N.
Дата публикации: 2020
Издатель: American Chemical Society
Библиографическое описание: Dibenzo[ f,h]furazano[3,4- b]quinoxalines: Synthesis by Intramolecular Cyclization through Direct Transition Metal-Free C-H Functionalization and Electrochemical, Photophysical, and Charge Mobility Characterization / Y. A. Kvashnin, E. V. Verbitskiy, O. S. Eltsov, P. A. Slepukhin, et al. . — DOI 10.1021/acsomega.0c00479 // ACS Omega. — 2020. — Vol. 14. — Iss. 5. — P. 8200-8210.
Аннотация: Herein, we describe the synthesis of unsymmetrically substituted dibenzo[f,h]furazano[3,4-b]quinoxalines by intramolecular cyclization through direct transition metal-free C-H functionalization. The electrochemical and photophysical properties for several polycycles have been measured. In thin films of the dibenzo[f,h]furazano[3,4-b]quinoxalines, hole mobility is in the order of 10-4 cm2 V-1 s-1. The results show that the HOMO and LUMO energy levels are appropriate for using the compounds as hole-transport materials in thin-film devices, in particular, organic and perovskite solar cells. Copyright © 2020 American Chemical Society.
URI: http://elar.urfu.ru/handle/10995/90570
Условия доступа: info:eu-repo/semantics/openAccess
Идентификатор SCOPUS: 85082876203
Идентификатор WOS: 000526342300050
Идентификатор PURE: 12670670
ISSN: 2470-1343
DOI: 10.1021/acsomega.0c00479
Сведения о поддержке: Russian Foundation for Basic Research, RFBR: 18-33-00103-mol_a
Russian Science Foundation, RSF: 18-13-00409
The research was financially supported by the Russian Science Foundation (project no. 18-13-00409). Y.A.K would like to acknowledge the financial support for the part of the synthetic section from the Russian Foundation for Basic Research (research project no. 18-33-00103-mol_a). The authors are grateful to Grigory A. Kim for carrying out the DFT calculations, which were performed by using “Uran” supercomputer of the Institute of Mathematics and Mechanics of the Ural Branch of the Russian Academy of Sciences. NMR experiments were carried out by using equipment of the Center for Joint Use “Spectroscopy and Analysis of Organic Compounds” at the Postovsky Institute of Organic Synthesis of the Ural Branch of the Russian Academy of Sciences.
Карточка проекта РНФ: 18-13-00409
Располагается в коллекциях:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

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