Anthra[2,3-b]benzo[d]thiophene: An Air-Stable Asymmetric Organic Semiconductor with High Mobility at Room Temperature
Source abstract
Abstract
An asymmetric heteroacene compound anthra[2,3-b]benzo[d]thiophene has been facilely synthesized. FETs fabricated with the compound exhibit a mobility as high as 0.41 cm2 V−1 s−1 at room temperature. High mobility and good stability suggest that exploration of asymmetric organic semiconductors would be extremely promising for the application in organic electronics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Memory and Neural Computing · Molecular Junctions and Nanostructures · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Beijing National Laboratory for Molecular Science, Key Laboratory of Organic Solids, Institute of Chemistry, and Graduate School, Chinese Academy of Sciences, Beijing 100190, China
References (29)
Show source-provided references
1. Katz H. E. · Acc. Chem. Res. · 2001 · 34 · 35910.1021/ar990114j ↗
2. Sun Y. · J. Mater. Chem. · 2005 · 15 · 5310.1039/b411245h ↗
3. Murphy A. R. · Chem. Rev. · 2007 · 107 · 106610.1021/cr0501386 ↗
4. Di C.-a. · J. Phys. Chem. B · 2007 · 111 · 1408310.1021/jp071753b ↗
5. Takimiya K. · Chem. Lett. · 2007 · 36 · 57810.1246/cl.2007.578 ↗
6. Lin Y. · IEEE Trans. Electron. Devices · 1997 · 44 · 132510.1109/16.605476 ↗
7. Kelley T. · Mater. Res. Symp. Proc. · 2003 · 771 · L6.5.110.1557/PROC-771-L6.5 ↗
8. Ito K. · Angew. Chem., Int. Ed. · 2003 · 42 · 115910.1002/anie.200390305 ↗
9. Yamada M. · Bull. Chem. Soc. Jpn. · 1988 · 61 · 105710.1246/bcsj.61.1057 ↗
10. Xiao K. · J. Am. Chem. Soc. · 2005 · 127 · 1328110.1021/ja052816b ↗
11. Anthony J. E. · Chem. Rev. · 2006 · 106 · 502810.1021/cr050966z ↗
12. Gao J. · Adv. Mater. · 2007 · 19 · 300810.1002/adma.200701167 ↗
13. Tang M. L. · J. Am. Chem. Soc. · 2006 · 128 · 1600210.1021/ja066824j ↗
14. Ebata H. · Org. Lett. · 2007 · 9 · 449910.1021/ol701815j ↗
15. Laquindanum J. G. · J. Am. Chem. Soc. · 1998 · 120 · 66410.1021/ja9728381 ↗
16. Werz D. B. · J. Am. Chem. Soc. · 2002 · 124 · 1063810.1021/ja027146d ↗
17. Valiyev F. · Chem. Mater. · 2007 · 19 · 301810.1021/cm070472d ↗
18. Tang M. L. · Chem. Mater. · 2006 · 18 · 625010.1021/cm0623514 ↗
19. Deman A. L. · Synth. Met. · 2004 · 146 · 36510.1016/j.synthmet.2004.08.015 ↗
20. Tedjamulia M. L. · J. Heterocyclic Chem. · 1983 · 20 · 86110.1002/jhet.5570200405 ↗
21. Mayer F. · Ann. Chem. · 259
22. Briseno A. L. · J. Am. Chem. Soc. · 2006 · 128 · 1557610.1021/ja066088j ↗
23. Bromley S. T. · J. Am. Chem. Soc. · 2004 · 126 · 654410.1021/ja049762a ↗
24. Rowland R. S. · J. Phys. Chem. · 1996 · 100 · 738410.1021/jp953141+ ↗
25. Gao X. · J. Chem. Crystallogr. · 2005 · 35 · 10710.1007/s10870-005-2798-z ↗
26. Meng H. · Adv. Mater. · 2003 · 15 · 109010.1002/adma.200304935 ↗
27. Meng H. · Chem. Mater. · 2003 · 15 · 177810.1021/cm020866z ↗
28. Li D. · Appl. Phys. Lett. · 2005 · 86 · 4210510.1063/1.1852708 ↗
29. DeLongchamp D. M. · Adv. Mater. · 2005 · 17 · 234010.1002/adma.200500263 ↗