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Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines. / Kvashnin, Yu. A.; Krynina, E. M.; Medvedeva, M. V. et al.
In: Russian Chemical Bulletin, Vol. 72, No. 4, 2023, p. 939-947.

Research output: Contribution to journal › Article › peer-review

Harvard

Kvashnin, YA, Krynina, EM, Medvedeva, MV, Svalova, TS, Kozitsina, AN, Eltsov, OS, Rusinov, GL, Verbitskiy, EV & Charushin, VN 2023, 'Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines', Russian Chemical Bulletin, vol. 72, no. 4, pp. 939-947. https://doi.org/10.1007/s11172-023-3857-3

APA

Kvashnin, Y. A., Krynina, E. M., Medvedeva, M. V., Svalova, T. S., Kozitsina, A. N., Eltsov, O. S., Rusinov, G. L., Verbitskiy, E. V., & Charushin, V. N. (2023). Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines. Russian Chemical Bulletin, 72(4), 939-947. https://doi.org/10.1007/s11172-023-3857-3

Vancouver

Kvashnin YA, Krynina EM, Medvedeva MV, Svalova TS, Kozitsina AN, Eltsov OS et al. Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines. Russian Chemical Bulletin. 2023;72(4):939-947. doi: 10.1007/s11172-023-3857-3

Author

Kvashnin, Yu. A. ; Krynina, E. M. ; Medvedeva, M. V. et al. / Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines. In: Russian Chemical Bulletin. 2023 ; Vol. 72, No. 4. pp. 939-947.

BibTeX

@article{2239b5232ca74b1fbe009b6810d67cb8,
title = "Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines",
abstract = "A simple synthetic route to hard-to-prepare polycyclic (hetero)aromatic compounds with the [1,2,5]chalcogenodiazolo[3,4-b]pyrazine scaffold was developed based on the intramolecular nucleophilic aromatic hydrogen substitution reaction. Electrochemical and photophysical measurements demonstrated that the synthesized polycyclic systems can be considered as narrow-bandgap (from 1.25 to 1.44 eV) n-type organic semiconductors, the energy levels of which are comparable to those of commercially available electronic semiconductors. {\textcopyright} 2023, Springer Science+Business Media LLC.",
author = "Kvashnin, {Yu. A.} and Krynina, {E. M.} and Medvedeva, {M. V.} and Svalova, {T. S.} and Kozitsina, {A. N.} and Eltsov, {O. S.} and Rusinov, {G. l.} and Verbitskiy, {E. V.} and Charushin, {V. N.}",
note = "The study was financially supported by the Ministry of Science and Higher Education of the Russian Federation within the framework of the Program of the Development of the Ural Federal University named after the first President of Russia B. N. Yeltsin under the Federal Academic Leadership Programme “Priority 2030”.",
year = "2023",
doi = "10.1007/s11172-023-3857-3",
language = "English",
volume = "72",
pages = "939--947",
journal = "Russian Chemical Bulletin",
issn = "1066-5285",
publisher = "Springer",
number = "4",

}

RIS

TY - JOUR

T1 - Synthesis of new polycyclic systems based on [1,2,5]chalcogenodiazolo[3,4-b]thieno[3,2-h]quinoxalines

AU - Kvashnin, Yu. A.

AU - Krynina, E. M.

AU - Medvedeva, M. V.

AU - Svalova, T. S.

AU - Kozitsina, A. N.

AU - Eltsov, O. S.

AU - Rusinov, G. l.

AU - Verbitskiy, E. V.

AU - Charushin, V. N.

N1 - The study was financially supported by the Ministry of Science and Higher Education of the Russian Federation within the framework of the Program of the Development of the Ural Federal University named after the first President of Russia B. N. Yeltsin under the Federal Academic Leadership Programme “Priority 2030”.

PY - 2023

Y1 - 2023

N2 - A simple synthetic route to hard-to-prepare polycyclic (hetero)aromatic compounds with the [1,2,5]chalcogenodiazolo[3,4-b]pyrazine scaffold was developed based on the intramolecular nucleophilic aromatic hydrogen substitution reaction. Electrochemical and photophysical measurements demonstrated that the synthesized polycyclic systems can be considered as narrow-bandgap (from 1.25 to 1.44 eV) n-type organic semiconductors, the energy levels of which are comparable to those of commercially available electronic semiconductors. © 2023, Springer Science+Business Media LLC.

AB - A simple synthetic route to hard-to-prepare polycyclic (hetero)aromatic compounds with the [1,2,5]chalcogenodiazolo[3,4-b]pyrazine scaffold was developed based on the intramolecular nucleophilic aromatic hydrogen substitution reaction. Electrochemical and photophysical measurements demonstrated that the synthesized polycyclic systems can be considered as narrow-bandgap (from 1.25 to 1.44 eV) n-type organic semiconductors, the energy levels of which are comparable to those of commercially available electronic semiconductors. © 2023, Springer Science+Business Media LLC.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85159179260

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000986557800012

U2 - 10.1007/s11172-023-3857-3

DO - 10.1007/s11172-023-3857-3

M3 - Article

VL - 72

SP - 939

EP - 947

JO - Russian Chemical Bulletin

JF - Russian Chemical Bulletin

SN - 1066-5285

IS - 4

ER -

ID: 39198341