journal article·2020

One-step synthesis of an acceptor–donor–acceptor small molecule based on indacenodithieno[3,2- b ]thiophene and benzothiadiazole units for high-performance solution-processed organic field-effect transistors

Guobing Zhang, Ruikun Chen, Mingxiang Sun, Minkyu Kim, Weiwei Wang, Longzhen Qiu, Kilwon Cho, Yunsheng Ding

Journal of Materials Chemistry C· Volume 8· Issue 40
Publisher page

Abstract

We reported a one-step synthesis of a high-performance acceptor–donor–acceptor small molecule based on indacenodithieno[3,2- b ]thiophene (IDTT) as the donor unit and benzothiadiazole (BT) as the acceptor unit.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Molecular Junctions and Nanostructures

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Special Display and Imaging Technology Innovation Center of Anhui Province

State Key Laboratory of Advanced Display Technology

Academy of Opto-Electronic Technology

Hefei University of Technology

Hefei

Department of Chemical Engineering

Pohang University of Science and Technology

Pohang

Korea

School of Chemistry and Chemical Engineering

Key Laboratory of Advance Functional Materials and Devices of Anhui Province

P. R. China

Funding

National Natural Science Foundation of China · National Basic Research Program of China · Fundamental Research Funds for the Central Universities

References (35)

Show source-provided references
1. Klauk · Chem. Soc. Rev. · 2010 · 39 · 264310.1039/b909902f ↗
2. Matsuhisa · Chem. Soc. Rev. · 2019 · 48 · 294610.1039/C8CS00814K ↗
3. Yuvaraja · Chem. Soc. Rev. · 2020 · 49 · 342310.1039/C9CS00811J ↗
4. Guo · Chem. Rev. · 2014 · 114 · 894310.1021/cr500225d ↗
5. Kang · J. Am. Chem. Soc. · 2016 · 138 · 367910.1021/jacs.5b10445 ↗
6. Fei · J. Am. Chem. Soc. · 2017 · 139 · 855210.1021/jacs.7b03099 ↗
7. Huang · Chem. Mater. · 2016 · 28 · 220910.1021/acs.chemmater.6b00154 ↗
8. Wang · Chem. Mater. · 2018 · 30 · 545110.1021/acs.chemmater.8b02359 ↗
9. Zhang · Adv. Mater. · 2016 · 28 · 392210.1002/adma.201504092 ↗
10. Liu · Macromolecules · 2018 · 51 · 37010.1021/acs.macromol.7b02309 ↗
11. Yang · Adv. Mater. · 2017 · 29 · 160616210.1002/adma.201606162 ↗
12. Lee · Chem. Sci. · 2017 · 8 · 294210.1039/C6SC04129A ↗
13. Nahid · Adv. Funct. Mater. · 2017 · 27 · 160474410.1002/adfm.201604744 ↗
14. Cai · Chem. Mater. · 2013 · 25 · 47110.1021/cm303793g ↗
15. Mas-Torrent · Chem. Soc. Rev. · 2008 · 37 · 82710.1039/b614393h ↗
16. Allard · Angew. Chem., Int. Ed. · 2008 · 47 · 407010.1002/anie.200701920 ↗
17. Zhang · Chem. Mater. · 2019 · 31 · 202710.1021/acs.chemmater.8b05054 ↗
18. Shin · Adv. Funct. Mater. · 2013 · 23 · 36610.1002/adfm.201201389 ↗
19. Choi · Nat. Mater. · 2017 · 17 · 210.1038/nmat5035 ↗
20. Paterson · Adv. Mater. · 2018 · 30 · 180107910.1002/adma.201801079 ↗
21. Yang · Adv. Funct. Mater. · 2020 · 30 · 190388910.1002/adfm.201903889 ↗
22. Yi · Adv. Mater. · 2011 · 23 · 580710.1002/adma.201103305 ↗
23. Zhou · J. Mater. Chem. C · 2019 · 7 · 1393910.1039/C9TC05038H ↗
24. Wang · Adv. Sci. · 2019 · 6 · 190241210.1002/advs.201902412 ↗
25. Xu · Adv. Mater. · 2012 · 24 · 635610.1002/adma.201203246 ↗
26. Song · Adv. Funct. Mater. · 2018 · 28 · 180289510.1002/adfm.201802895 ↗
27. Zhang · Adv. Mater. · 2016 · 28 · 392210.1002/adma.201504092 ↗
28. Fei · J. Am. Chem. Soc. · 2017 · 139 · 855210.1021/jacs.7b03099 ↗
29. Song · Adv. Funct. Mater. · 2018 · 28 · 180289510.1002/adfm.201802895 ↗
30. Zhao · Adv. Mater. · 2017 · 29 · 160241010.1002/adma.201602410 ↗
31. Spano · Acc. Chem. Res. · 2010 · 43 · 42910.1021/ar900233v ↗
32. Guiglion · Macromol. Chem. Phys. · 2016 · 217 · 34410.1002/macp.201500432 ↗
33. Alvarez · Dalton Trans. · 2013 · 42 · 861710.1039/c3dt50599e ↗
34. Zang · Acc. Chem. Res. · 2008 · 41 · 159610.1021/ar800030w ↗
35. Gao · J. Mater. Chem. · 2018 · 6 · 1249810.1039/C8TC05327H ↗