journal article·2017-11-01

Unconventional Molecular Design Approach of High-Efficiency Deep Blue Thermally Activated Delayed Fluorescent Emitters Using Indolocarbazole as an Acceptor

Jeong-A Seo, Yirang Im, Si Hyun Han, Chil Won Lee, Jun Yeob Lee

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Abstract

Unconventional blue thermally activated delayed fluorescent emitters having electron-donating type indolocarbazole as an acceptor were developed by attaching carbazolylcarbazole or acridine donors to the indolocarbazole acceptor. Three compounds were derived from the indolocarbazole acceptor. The indolocarbazole-acridine combined products showed efficient delayed fluorescent behavior and a high quantum efficiency of 19.5% with a color coordinate of (0.15, 0.16) when they were evaluated as thermally activated delayed fluorescent emitters in deep blue fluorescent devices. This is the first demonstration of the use of electron-donating carbazole-derived moieties as efficient acceptor units of blue thermally activated delayed fluorescent emitters.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Luminescence and Fluorescent Materials · Organic Electronics and Photovoltaics

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

Affiliations

School of Chemical Engineering, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon, Gyeonggi 440-746, Korea

Department of Chemistry, Dankook University, Cheonan, Chungcheongnam-do 31116, Korea

Funding

National Research Foundation of Korea

References (36)

Show source-provided references
1. 10.1002/adfm.20150299510.1002/adfm.201502995 ↗
2. 10.1002/adma.20130075310.1002/adma.201300753 ↗
3. 10.1021/jacs.5b1095010.1021/jacs.5b10950 ↗
4. 10.1021/acs.chemmater.5b0251510.1021/acs.chemmater.5b02515 ↗
5. 10.1002/adma.20140253210.1002/adma.201402532 ↗
6. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
7. 10.1002/adfm.20160352010.1002/adfm.201603520 ↗
8. 10.1002/adfm.20150510610.1002/adfm.201505106 ↗
9. 10.1021/ja510144h10.1021/ja510144h ↗
10. 10.1021/ja306538w10.1021/ja306538w ↗
11. 10.1021/acsami.6b0587710.1021/acsami.6b05877 ↗
12. 10.1021/acsami.6b1067810.1021/acsami.6b10678 ↗
13. 10.1002/chem.20160168610.1002/chem.201601686 ↗
14. 10.1039/C3TC31936A10.1039/C3TC31936A ↗
15. 10.1021/acs.chemmater.6b0148410.1021/acs.chemmater.6b01484 ↗
16. 10.1016/j.orgel.2015.12.00110.1016/j.orgel.2015.12.001 ↗
17. 10.1039/C5CC07999C10.1039/C5CC07999C ↗
18. 10.1002/adfm.20160250110.1002/adfm.201602501 ↗
19. 10.1016/j.tetlet.2016.03.09710.1016/j.tetlet.2016.03.097 ↗
20. 10.1002/adma.20150026710.1002/adma.201500267 ↗
21. 10.1021/ja045614910.1021/ja0456149 ↗
22. 10.1016/j.tetlet.2015.12.05710.1016/j.tetlet.2015.12.057 ↗
23. 10.1016/0379-6779(96)80213-X10.1016/0379-6779(96)80213-X ↗
24. 10.1038/nmat415410.1038/nmat4154 ↗
25. 10.1016/j.orgel.2016.04.03610.1016/j.orgel.2016.04.036 ↗
26. 10.1002/adfm.20150207910.1002/adfm.201502079 ↗
27. 10.1021/ol500663b10.1021/ol500663b ↗
28. 10.1039/c2jm30207a10.1039/c2jm30207a ↗
29. 10.1002/chem.20110025410.1002/chem.201100254 ↗
30. 10.1063/1.162463910.1063/1.1624639 ↗
31. 10.1088/0022-3727/48/36/36510610.1088/0022-3727/48/36/365106 ↗
32. 10.1002/anie.20140299210.1002/anie.201402992 ↗
33. 10.1002/adma.20150101910.1002/adma.201501019 ↗
34. 10.1002/adma.20150549110.1002/adma.201505491 ↗
35. 10.1016/j.dyepig.2016.09.01310.1016/j.dyepig.2016.09.013 ↗
36. 10.1002/adma.20140034710.1002/adma.201400347 ↗