First N-Borylated Emitters Displaying Highly Efficient Thermally Activated Delayed Fluorescence and High-Performance OLEDs
Source abstract
Abstract
Despite the fast boom of thermally activated delayed fluorescence (TADF) emitters bearing borane-based acceptor, so far, no TADF emitter with a direct B-N linkage between N-donor and boryl acceptor has been reported. The latter should simplify the molecular architecture and hence facilitate the synthetic design and versatility. We report here the preparation and characterization of a new series of N-borylated compounds with functional acridine donor unit; namely: ACBM, PACBM, and SACBM. Spectroscopic studies were performed to explore their photophysical properties that exhibited prominent solvatochromism and thermally activated delayed fluorescence. The time-dependent DFT calculation indicated the involvement of substantial intramolecular charge transfer character for which HOMO and LUMO are spatially separated. For compound SACBM, fabrication of green emitting OLED gave CIE chromaticity of (0.22, 0.59) and maximum external quantum efficiency, luminance efficiency and power efficiency of 19.1%, 60.9 cd/A, and 43.6 lm/W, respectively, demonstrating for the first time the highly efficient OLEDs using N-borylated TADF emitters.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan
Department of Chemistry, National Taiwan University, Taipei 10617, Taiwan
Department of Photonics Engineering, Yuan Ze University, Chungli 32003, Taiwan
Funding
Ministry of Science and Technology, Taiwan
References (69)
Show source-provided references
1. 10.1021/ja306538w10.1021/ja306538w ↗
2. 10.1002/adfm.20130338910.1002/adfm.201303389 ↗
3. 10.1038/nature1168710.1038/nature11687 ↗
4. 10.1039/c3tc30699b10.1039/c3tc30699b ↗
5. 10.1039/C5CP02810H10.1039/C5CP02810H ↗
6. 10.1039/C5CC09797E10.1039/C5CC09797E ↗
7. 10.1038/nphoton.2014.1210.1038/nphoton.2014.12 ↗
8. 10.1021/acs.chemmater.5b0201210.1021/acs.chemmater.5b02012 ↗
9. 10.1002/anie.20140299210.1002/anie.201402992 ↗
10. 10.1002/adma.20150628610.1002/adma.201506286 ↗
11. 10.1021/acs.chemmater.6b0169110.1021/acs.chemmater.6b01691 ↗
12. 10.1002/adma.20130075310.1002/adma.201300753 ↗
13. 10.1002/adma.20150596310.1002/adma.201505963 ↗
14. 10.1002/adom.20150068910.1002/adom.201500689 ↗
15. 10.1039/C5TC03849A10.1039/C5TC03849A ↗
16. 10.1038/ncomms947610.1038/ncomms9476 ↗
17. 10.1039/C5TC00279F10.1039/C5TC00279F ↗
18. 10.1021/acs.jpcc.5b0911410.1021/acs.jpcc.5b09114 ↗
19. 10.1039/C5CC09645F10.1039/C5CC09645F ↗
20. 10.1039/C5TC04057D10.1039/C5TC04057D ↗
21. 10.1002/chem.20160168610.1002/chem.201601686 ↗
22. 10.1021/acsami.5b0564810.1021/acsami.5b05648 ↗
23. 10.1039/C5CC04126K10.1039/C5CC04126K ↗
24. 10.1002/adom.20150001610.1002/adom.201500016 ↗
25. 10.1021/acsami.6b1479610.1021/acsami.6b14796 ↗
26. 10.1039/C6CS00368K10.1039/C6CS00368K ↗
27. 10.1002/adma.20160544410.1002/adma.201605444 ↗
28. 10.1088/2050-6120/aa537e10.1088/2050-6120/aa537e ↗
29. 10.1039/C6SC04245G10.1039/C6SC04245G ↗
30. 10.1002/anie.20150827010.1002/anie.201508270 ↗
31. 10.1016/j.tetlet.2016.09.07210.1016/j.tetlet.2016.09.072 ↗
32. 10.1039/C6TC01353H10.1039/C6TC01353H ↗
33. 10.1039/C5CC00307E10.1039/C5CC00307E ↗
34. 10.1246/bcsj.2015039910.1246/bcsj.20150399 ↗
35. 10.1002/anie.20150633510.1002/anie.201506335 ↗
36. 10.1002/adma.20150549110.1002/adma.201505491 ↗
37. 10.1039/c3cs60170f10.1039/c3cs60170f ↗
38. 10.1002/anie.20150923110.1002/anie.201509231 ↗
39. 10.1002/chem.20160241010.1002/chem.201602410 ↗
40. 10.1039/C6TC04994J10.1039/C6TC04994J ↗
41. 10.1039/B703366D10.1039/B703366D ↗
42. 10.1039/C2DT32134C10.1039/C2DT32134C ↗
43. 10.1002/anie.20160945910.1002/anie.201609459 ↗
44. 10.1021/jo200280c10.1021/jo200280c ↗
45. 10.1039/C6CC02856J10.1039/C6CC02856J ↗
46. 10.1002/adfm.20040008110.1002/adfm.200400081 ↗
47. 10.1021/ic048974610.1021/ic0489746 ↗
48. 10.1002/adfm.20040025010.1002/adfm.200400250 ↗
49. 10.1021/ol061966410.1021/ol0619664 ↗
50. 10.1007/BF0067201410.1007/BF00672014 ↗
51. 10.1002/zaac.20090042210.1002/zaac.200900422 ↗
52. 10.1021/jp501017f10.1021/jp501017f ↗
53. 10.1039/C6SC04863C10.1039/C6SC04863C ↗
54. 10.1038/ncomms1498710.1038/ncomms14987 ↗
55. 10.1016/j.dyepig.2017.01.05510.1016/j.dyepig.2017.01.055 ↗
56. 10.1039/c2jm14686j10.1039/c2jm14686j ↗
57. 10.1016/S1566-1199(01)00010-610.1016/S1566-1199(01)00010-6 ↗
58. 10.1021/cm703682q10.1021/cm703682q ↗
59. 10.1016/j.orgel.2011.01.02110.1016/j.orgel.2011.01.021 ↗
60. 10.1021/cm800498510.1021/cm8004985 ↗
61. 10.1063/1.156814610.1063/1.1568146 ↗
62. 10.1016/j.orgel.2009.07.02010.1016/j.orgel.2009.07.020 ↗
63. 10.1039/c3tc00919j10.1039/c3tc00919j ↗
64. 10.1002/adma.20070173010.1002/adma.200701730 ↗
65. 10.1063/1.212614010.1063/1.2126140 ↗
66. 10.1063/1.214171810.1063/1.2141718 ↗
67. 10.1002/adfm.20130054710.1002/adfm.201300547 ↗
68. 10.1002/adma.20140454610.1002/adma.201404546 ↗
69. 10.1021/am401694s10.1021/am401694s ↗