The impact of structural modification on the electrochromic and electroluminescent properties of D–A–D benzothiadiazole derivatives with a fluorene linker and (Bi)thiophene units
Source abstract
Abstract
Two derivatives of benzothiadiazole (BTD) symmetrically functionalized with a dihexylfluorene units serving as a linker between the BTD core and the thiophene or bithiophene were designed, synthesized and comprehensively characterized.
Only a short abstract or summary was supplied by the source.
Source: crossref · Quality: short
Research context
OpenAlex topics: Conducting polymers and applications · Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Faculty of Chemistry, Warsaw University of Technology, Warsaw, Poland
Cardinal Stefan Wyszynski University, Faculty of Mathematics and Natural Sciences, School of Exact Sciences, Warsaw, Poland
Faculty of Chemistry, Silesian University of Technology, Gliwice, Poland
Centre for Organic and Nanohybrid Electronics, Silesian University of Technology, Gliwice, Poland
Department of Physics, Durham University, Durham, UK
Funding
Narodowe Centrum Nauki
References (58)
Show source-provided references
1. Soylemez · Org. Electron. · 2019 · 65 · 32710.1016/j.orgel.2018.11.001 ↗
2. Balan · Polym. Chem. · 2011 · 2 · 102910.1039/c1py00007a ↗
3. Baran · Chem. Mater. · 2010 · 22 · 297810.1021/cm100372t ↗
4. Di · Acc. Chem. Res. · 2019 · 52 · 111310.1021/acs.accounts.9b00031 ↗
5. Shen · ACS Appl. Electron. Mater. · 2021 · 3 · 243410.1021/acsaelm.1c00312 ↗
6. Hueso · Adv. Mater. · 2007 · 19 · 263910.1002/adma.200602748 ↗
7. Tsuneyasu · Chem. Lett. · 2016 · 45 · 94910.1246/cl.160361 ↗
8. Tsuneyasu · Jpn. J. Appl. Phys. · 2016 · 55 · 110.7567/JJAP.55.041601 ↗
9. Tsuneyasu · Adv. Mater. Technol. · 2021 · 6 · 200088110.1002/admt.202000881 ↗
10. Gingras · Chem. – Eur. J. · 2008 · 14 · 1035710.1002/chem.200801198 ↗
11. Hsiao · J. Polym. Res. · 2015 · 22 · 10710.1007/s10965-015-0754-y ↗
12. Sun · Polym. Chem. · 2016 · 7 · 605510.1039/c6py01345g ↗
13. Sun · Macromolecules · 2019 · 52 · 513110.1021/acs.macromol.9b00079 ↗
14. Sun · RSC Adv. · 2016 · 6 · 6628810.1039/c6ra12174h ↗
15. Kanazawa · Sol. Energy Mater. Sol. Cells · 2016 · 145 · 4210.1016/j.solmat.2015.06.061 ↗
16. Kanazawa · J. Phys. Chem. A · 2014 · 118 · 602610.1021/jp5060588 ↗
17. Wu · Adv. Funct. Mater. · 2014 · 24 · 642210.1002/adfm.201401608 ↗
18. Al-kutubi · Eur. Polym. J. · 2016 · 83 · 47810.1016/j.eurpolymj.2016.04.033 ↗
19. Guermazi · J. Fluoresc. · 2016 · 310.1007/s10895-016-1822-3 ↗
20. Audebert · Chem. Sci. · 2013 · 4 · 57510.1039/c2sc21503a ↗
21. Koldemir · J. Mater. Chem. · 2011 · 21 · 648010.1039/c1jm10345h ↗
22. Carbas · Org. Electron. Phys. Mater. Appl. · 2014 · 15 · 50010.1016/j.orgel.2013.12.003 ↗
23. Schmatz · J. Polym. Sci. Part A Polym. Chem. · 2018 · 56 · 14710.1002/pola.28896 ↗
24. Zhao · Angew. Chem., Int. Ed. · 2020 · 59 · 1904210.1002/anie.202008885 ↗
25. Pluczyk · Electrochim. Acta · 2016 · 216 · 16010.1016/j.electacta.2016.09.009 ↗
26. Pluczyk · RSC Adv. · 2015 · 5 · 740110.1039/C4RA12603C ↗
27. Li · Angew. Chem., Int. Ed. · 2021 · 60 · 1484610.1002/anie.202103070 ↗
28. Nasiri · J. Lumin. · 2020 · 220 · 11695510.1016/j.jlumin.2019.116955 ↗
29. Frizon · Dyes Pigm. · 2016 · 135 · 2610.1016/j.dyepig.2016.07.011 ↗
30. Pathak · J. Org. Chem. · 2017 · 82 · 1151210.1021/acs.joc.7b02127 ↗
31. Huang · Sol. Energy Mater. Sol. Cells · 2006 · 90 · 49110.1016/j.solmat.2005.02.016 ↗
32. Chang · J. Mater. Chem. C · 2020 · 8 · 1612910.1039/d0tc03680c ↗
33. Fabrizi De Biani · RSC Adv. · 2018 · 8 · 1083610.1039/c7ra13242e ↗
34. Yan · New J. Chem. · 2019 · 43 · 956610.1039/c9nj01730e ↗
35. Bezgin Carbas · Polymer · 2022 · 254 · 12504010.1016/j.polymer.2022.125040 ↗
36. Moreira · Adv. Electron. Mater. · 2021 · 7 · 210016610.1002/aelm.202100166 ↗
37. Lv · J. Mater. Chem. C · 2017 · 5 · 1210.1039/C6TC04002K ↗
38. Taylor-Shaw · J. Mater. Chem. C · 2016 · 4 · 1149910.1039/c6tc03585J ↗
39. Huang · J. Am. Chem. Soc. · 2011 · 133 · 802810.1021/ja202144v ↗
40. Neese · WIREs Comput. Mol. Sci. · 2018 · 8 · e132710.1002/wcms.1327 ↗
41. Neese · Wiley Interdiscip. Rev.: Comput. Mol. Sci. · 2012 · 2 · 7310.1002/wcms.81 ↗
42. Lehtola · SoftwareX · 2018 · 7 · 110.1016/j.softx.2017.11.002 ↗
43. Strickler · J. Chem. Phys. · 1962 · 37 · 81410.1063/1.1733166 ↗
44. Matulaitis · Dyes Pigm. · 2016 · 127 · 4510.1016/j.dyepig.2015.11.001 ↗
45. Belyaev · Inorg. Chem. Front. · 2020 · 7 · 14010.1039/c9qi01015g ↗
46. Chen · J. Org. Chem. · 2012 · 77 · 219210.1021/jo202215x ↗
47. Xu · Adv. Opt. Mater. · 2020 · 8 · 190214210.1002/adom.201902142 ↗
48. Ahmad · J. Mater. Chem. C · 2022 · 10 · 478510.1039/d1tc04748e ↗
49. Ledwon · RSC Adv. · 2015 · 5 · 7730310.1039/c5ra06993a ↗
50. Pashazadeh · J. Phys. Chem. Lett. · 2018 · 9 · 117210.1021/acs.jpclett.8b00136 ↗
51. Wei · Chem. Mater. · 1991 · 3 · 88810.1021/cm00017a026 ↗
52. Roncali · Chem. Rev. · 1992 · 92 · 71110.1021/cr00012a009 ↗
53. Idzik · Electrochim. Acta · 2010 · 55 · 741910.1016/j.electacta.2010.07.005 ↗
54. Audebert · J. Phys. Chem. B · 1998 · 102 · 866110.1021/jp9804289 ↗
55. Karaman · J. Electroanal. Chem. · 2021 · 895 · 11548310.1016/j.jelechem.2021.115483 ↗
56. Scalon · ACS Appl. Polym. Mater. · 2021 · 3 · 422310.1021/acsapm.1c00651 ↗
57. Jensen · J. Mater. Chem. C · 2013 · 1 · 482610.1039/c3tc30751d ↗
58. Koyuncu · J. Mater. Chem. · 2011 · 21 · 268410.1039/c0jm02366c ↗