Home / Publications / Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics

Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics

Sergey Dmitrievich Tokarev 1
Sergey Dmitrievich Tokarev
, 
Yulia Andreevna Sotnikova 1
Yulia Andreevna Sotnikova
, 
Alexander Vladimirovich Anisimov 1
Alexander Vladimirovich Anisimov
, 
Yurii Viktorovich Fedorov 2
Yurii Viktorovich Fedorov
, 
Gediminas Jonusauskas 3
Gediminas Jonusauskas
, 
Dmitry Alexandrovich Lypenko 4
Dmitry Alexandrovich Lypenko
, 
Vladimir Vladimirovich Malov 4
Vladimir Vladimirovich Malov
, 
Alexey Raisovich Tameev 4
Alexey Raisovich Tameev
, 
Eugene Ivanovich Mal'tsev 4
Eugene Ivanovich Mal'tsev
, 
Olga Anatol'evna Fedorova 1, 2
Olga Anatol'evna Fedorova
10.1016/j.mencom.2019.09.030
Published 2019-09-04
Communication , Volume 29, Issue 5, 567-569
6
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Tokarev S. D. et al. Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics // Mendeleev Communications. 2019. Vol. 29. No. 5. pp. 567-569.
GOST all authors (up to 50) Copy
Tokarev S. D., Sotnikova Y. A., Anisimov A. V., Fedorov Y. V., Jonusauskas G., Lypenko D. A., Malov V. V., Tameev A. R., Mal'tsev E. I., Fedorova O. A. Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics // Mendeleev Communications. 2019. Vol. 29. No. 5. pp. 567-569.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1016/j.mencom.2019.09.030
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.030
TI - Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics
T2 - Mendeleev Communications
AU - Tokarev, Sergey Dmitrievich
AU - Sotnikova, Yulia Andreevna
AU - Anisimov, Alexander Vladimirovich
AU - Fedorov, Yurii Viktorovich
AU - Jonusauskas, Gediminas
AU - Lypenko, Dmitry Alexandrovich
AU - Malov, Vladimir Vladimirovich
AU - Tameev, Alexey Raisovich
AU - Mal'tsev, Eugene Ivanovich
AU - Fedorova, Olga Anatol'evna
PY - 2019
DA - 2019/09/04
PB - Mendeleev Communications
SP - 567-569
IS - 5
VL - 29
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{2019_Tokarev,
author = {Sergey Dmitrievich Tokarev and Yulia Andreevna Sotnikova and Alexander Vladimirovich Anisimov and Yurii Viktorovich Fedorov and Gediminas Jonusauskas and Dmitry Alexandrovich Lypenko and Vladimir Vladimirovich Malov and Alexey Raisovich Tameev and Eugene Ivanovich Mal'tsev and Olga Anatol'evna Fedorova},
title = {Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics},
journal = {Mendeleev Communications},
year = {2019},
volume = {29},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.030},
number = {5},
pages = {567--569},
doi = {10.1016/j.mencom.2019.09.030}
}
MLA
Cite this
MLA Copy
Tokarev, Sergey Dmitrievich, et al. “Donor–acceptor (E)-2-[2-(2,2′-bithiophen-5-yl)vinyl]benzo[d]thiazole: synthesis, optical, electrochemical studies and charge transport characteristics.” Mendeleev Communications, vol. 29, no. 5, Sep. 2019, pp. 567-569. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2019.09.030.

Abstract

Condensation of 2-methylbenzothiazole with 2,2′-bithiophene-5-carbaldehyde affords the title compound, a new chromophore. This compound was used for the doping of poly[9,9-bis(6-diethoxylphosphorylhexyl)fluorene], and the obtained composites demonstrated high electron mobility (1.50×10−4cm2V−1s−1) in contrast to dopant-free matrixes.

References

1.
Small Molecule Solution-Processed Bulk Heterojunction Solar Cells
Walker B., Kim C., Nguyen T.
Chemistry of Materials, 2010
2.
Solution processable D–A small molecules for bulk-heterojunction solar cells
Li Y., Guo Q., Li Z., Pei J., Tian W.
Energy and Environmental Science, 2010
4.
Photovoltaics from soluble small molecules
Lloyd M.T., Anthony J.E., Malliaras G.G.
Materials Today, 2007
5.
Solodukhin A.N., Luponosov Y.N., Buzin M.I., Peregudova S.M., Svidchenko E.A., Ponomarenko S.A.
Mendeleev Communications, 2018
6.
Lukovskaya E.V., Dyachenko N.V., Khoroshutin A.V., Bobyleva A.A., Anisimov A.V., Karnoukhova V.A., Jonusauskas G., Fedorov Y.V., Fedorova O.A.
Mendeleev Communications, 2018
7.
Nanoscale Phase Separation and High Photovoltaic Efficiency in Solution-Processed, Small-Molecule Bulk Heterojunction Solar Cells
Walker B., Tamayo A.B., Dang X., Zalar P., Seo J.H., Garcia A., Tantiwiwat M., Nguyen T.
Advanced Functional Materials, 2009
8.
A Solution-Processable Star-Shaped Molecule for High-Performance Organic Solar Cells
Shang H., Fan H., Liu Y., Hu W., Li Y., Zhan X.
Advanced Materials, 2011
9.
A Naphthodithiophene-Diketopyrrolopyrrole Donor Molecule for Efficient Solution-Processed Solar Cells
Loser S., Bruns C.J., Miyauchi H., Ortiz R.P., Facchetti A., Stupp S.I., Marks T.J.
Journal of the American Chemical Society, 2011
10.
Solution-processed bulk heterojunction organic solar cells based on an oligothiophene derivative
Yin B., Yang L., Liu Y., Chen Y., Qi Q., Zhang F., Yin S.
Applied Physics Letters, 2010
12.
Metal-free organic dyes for dye-sensitized solar cells: recent advances
Kanaparthi R.K., Kandhadi J., Giribabu L.
Tetrahedron, 2012
13.
Self-assembled semiconducting monolayers in organic electronics
Sizov A.S., Agina E.V., Ponomarenko S.A.
Russian Chemical Reviews, 2018
16.
Electron and ambipolar transport in organic field-effect transistors.
Zaumseil J., Sirringhaus H.
Chemical Reviews, 2007
17.
A high-mobility electron-transporting polymer for printed transistors
Yan H., Chen Z., Zheng Y., Newman C., Quinn J.R., Dötz F., Kastler M., Facchetti A.
Nature, 2009
18.
Ultralow-power organic complementary circuits
Klauk H., Zschieschang U., Pflaum J., Halik M.
Nature, 2007
21.
Organic light-emitting transistors with an efficiency that outperforms the equivalent light-emitting diodes.
Capelli R., Toffanin S., Generali G., Usta H., Facchetti A., Muccini M.
Nature Materials, 2010
22.
The photonic perspective of organic light‐emitting transistors
Muccini M., Koopman W., Toffanin S.
Laser and Photonics Reviews, 2011
24.
Photobehaviour of thio-analogues of stilbene and 1,4-distyrylbenzene studied by time-resolved absorption techniques
Ginocchietti G., Cecchetto E., De Cola L., Mazzucato U., Spalletti A.
Chemical Physics, 2008
27.
Balanced Carrier Mobilities: Not a Necessary Condition for High‐Efficiency Thin Organic Solar Cells as Determined by MIS‐CELIV
Armin A., Juska G., Ullah M., Velusamy M., Burn P.L., Meredith P., Pivrikas A.
Advanced Energy Materials, 2013
28.
Malov V.V., Ghosh T., Nair V.C., Maslov M.M., Katin K.P., Unni K.N., Tameev A.R.
Mendeleev Communications, 2019
29.
Charge Transport Characteristics of Diarylethene Photoswitching Single-Molecule Junctions
Kim Y., Hellmuth T.J., Sysoiev D., Pauly F., Pietsch T., Wolf J., Erbe A., Huhn T., Groth U., Steiner U.E., Scheer E.
Nano Letters, 2012