Benzothieno[2,3-b]thiophene semiconductors: synthesis, characterization and applications in organic field-effect transistors
Source abstract
Abstract
An efficient synthetic approach to a series of benzothieno[2,3-b]thiophene (BTT) derivatives used as an important core with different bridge spacers is described. Thermal properties of the present compounds are stable: neither phase transition nor thermal decomposition was observed up to 300 °C. The adjacent molecule crystal stackings are shifted affording a nearly 1/3 intermolecular π-overlap. The OFETs based on BTTB exhibit excellent field-effect performances with a mobility of 0.46 cm2 V−1 s−1 and on–off current ratios larger than 107 at room temperature. All the results demonstrate these benzothieno[2,3-b]thiophene derivatives as promising materials for optoelectronic devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (37)
Show source-provided references
1. Anthony · Chem. Rev. · 2006 · 106 · 502810.1021/cr050966z ↗
2. Lei · Org. Lett. · 2011 · 13 · 264210.1021/ol200748c ↗
3. Wu · Chem. Soc. Rev. · 2010 · 39 · 48910.1039/B813123F ↗
4. Lin · Adv. Mater. · 2012 · 24 · 308710.1002/adma.201200721 ↗
5. Hong · Org. Lett. · 2011 · 13 · 141010.1021/ol103013d ↗
6. Liu · Sci. China: Chem. · 2010 · 43 · 77910.1007/s11426-010-0130-z ↗
7. Liu · J. Phys. Chem. C · 2010 · 114 · 2231610.1021/jp1099464 ↗
8. Cai · Chem. Mater. · 2013 · 25 · 47110.1021/cm303793g ↗
9. Pho · J. Am. Chem. Soc. · 2012 · 134 · 1818510.1021/ja3082582 ↗
10. Mitsui · J. Am. Chem. Soc. · 2012 · 134 · 544810.1021/ja2120635 ↗
11. Xiao · J. Am. Chem. Soc. · 2005 · 127 · 1328110.1021/ja052816b ↗
12. Liu · Chem.–Asian J. · 2010 · 5 · 155010.1002/asia.201000001 ↗
13. Li · J. Am. Chem. Soc. · 1998 · 120 · 220610.1021/ja9735968 ↗
14. Tan · Adv. Funct. Mater. · 2009 · 19 · 27210.1002/adfm.200800933 ↗
15. Niimi · J. Am. Chem. Soc. · 2011 · 133 · 873210.1021/ja202377m ↗
16. Du · J. Phys. Chem. C · 2010 · 114 · 1056510.1021/jp101135e ↗
17. Gao · Adv. Mater. · 2007 · 19 · 300810.1002/adma.200701167 ↗
18. Huang · Org. Lett. · 2012 · 14 · 330010.1021/ol3012748 ↗
19. Sun · Adv. Funct. Mater. · 2006 · 16 · 42610.1002/adfm.200500547 ↗
20. Amin · J. Am. Chem. Soc. · 2012 · 134 · 1654810.1021/ja307802q ↗
21. Liu · Adv. Funct. Mater. · 2009 · 19 · 77210.1002/adfm.200800829 ↗
22. Liu · Chem.–Eur. J. · 2010 · 16 · 223110.1002/chem.200902755 ↗
23. Chen · J. Phys. Chem. C · 2011 · 115 · 2398410.1021/jp2081484 ↗
24. Gao · J. Org. Chem. · 2008 · 73 · 920710.1021/jo801898g ↗
25. Sirringhaus · J. Mater. Chem. · 1999 · 9 · 209510.1039/a902679g ↗
26. Du · Chem.–Eur. J. · 2009 · 15 · 827510.1002/chem.200900860 ↗
27. Gao · Adv. Mater. · 2009 · 21 · 21310.1002/adma.200802031 ↗
28. Du · Chem. Commun. · 2010 · 46 · 857310.1039/c0cc04147e ↗
29. Chapman · J. Chem. Soc. C · 1971 · 46310.1039/j39710000463 ↗
30. Sasaki · Tetrahedron · 1982 · 38 · 7510.1016/0040-4020(82)85048-5 ↗
31. Mathis · J. Appl. Phys. · 2014 · 115 · 04370710.1063/1.4863209 ↗
32. Chen · J. Phys. Chem. C · 2010 · 114 · 328010.1021/jp911139x ↗
33. Zhang · Chem. Mater. · 2006 · 18 · 347010.1021/cm0609348 ↗
34. Cervini · Synth. Met. · 1997 · 84 · 35910.1016/S0379-6779(97)80781-3 ↗
35. Gao · J. Mater. Chem. · 2007 · 17 · 73610.1039/B613093C ↗
36. Meng · Adv. Mater. · 2003 · 15 · 109010.1002/adma.200304935 ↗
37. Di · J. Phys. Chem. B · 2007 · 111 · 1408310.1021/jp071753b ↗