journal article·2002-09-01

Blue-Emitting Anthracenes with End-Capping Diarylamines

Krzysztof Danel, Tai-Hsiang Huang, Jiann T. Lin, Yu-Tai Tao, Chang-Hao Chuen

Chemistry of Materials· Volume 14· Issue 9
Publisher page

Abstract

A new series of 2- tert -butyl-9,10-bis(bromoaryl)anthracenes have been synthesized from 2- tert -butyl-9,10-anthraquinone. Palladium-catalyzed C−N bond formation between these bromo compounds and diarylamines provides stable 2- tert -butyl-9,10-diarylanthracenes containing two peripheral diarylamines ( anth ). They possess high thermal decomposition temperature ( T d > 450 °C) and form a stable glass ( T g > 130 °C). Furthermore, they are fluorescent in the blue region with moderate to good quantum efficiencies. Two types of light-emitting diodes (LED) were constructed from anth, (I) ITO/ anth /TPBI/Mg:Ag and (II) ITO/ anth /Alq 3 /Mg:Ag, where TPBI and Alq 3 are 1,3,5-tris( N -phenylbenzimidazol-2-yl)benzene and tris(8-hydroxyquinolinato)aluminum, respectively. In type I devices, the anth function as the hole-transporting and emitting material. In type II devices, emission from Alq 3 is observed. Several blue-light-emitting type I devices exhibit good maximum brightness and physical performance. The relation between the energy levels of the anth and the performance of the light-emitting diode is discussed.
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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

Institute of Chemistry, Academia Sinica, Taipei, Taiwan 115, Republic of China, and Department of Chemistry, National Central University, Chungli, Taiwan 320, Republic of China

References (56)

Show source-provided references
1. Miyata S. · 1997
2. Chen C. H. · Coord. Chem. Rev. · 1998 · 171 · 16110.1016/S0010-8545(98)90027-3 ↗
3. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
4. Burroughes J. H. · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
5. Hosokawa C. · Appl. Phys. Lett. · 1995 · 67 · 385310.1063/1.115295 ↗
6. Tamoto N. · Chem. Mater. · 1997 · 9 · 107710.1021/cm960391+ ↗
7. Tao X. T. · J. Am. Chem. Soc. · 1999 · 121 · 944710.1021/ja9924142 ↗
8. Gao Z. Q. · Appl. Phys. Lett. · 1999 · 74 · 86510.1063/1.123392 ↗
9. Kijima Y. · Jpn. J. Appl. Phys. · 1999 · 38 · 527410.1143/JJAP.38.5274 ↗
10. Tao Y. T. · Appl Phys. Lett. · 2000 · 77 · 93310.1063/1.1288811 ↗
11. Leung L. M. · J. Am. Chem. Soc. · 2000 · 122 · 564010.1021/ja000927z ↗
12. Tokito S. · Synth. Met. · 2000 · 111 · 39310.1016/S0379-6779(99)00381-1 ↗
13. Chan L.-H. · Adv. Mater. · 2001 · 13 · 163710.1002/1521-4095(200111)13:21<1637::AID-ADMA1637>3.0.CO;2-S ↗
14. Kim Y.-H. · Adv. Mater. · 2001 · 13 · 169010.1002/1521-4095(200111)13:22<1690::AID-ADMA1690>3.0.CO;2-K ↗
15. Liu Y. · Appl. Phys. Lett. · 2001 · 78 · 230010.1063/1.1366338 ↗
16. Im W.-B. · Appl. Phys. Lett. · 2001 · 79 · 138710.1063/1.1398604 ↗
17. Tao Y.-T. · J. Mater. Chem. · 2001 · 11 · 76810.1039/b007918i ↗
18. Chan L.-H. · J. Am. Chem. Soc. · 2002 · 124 · 646910.1021/ja0255150 ↗
19. Shirota Y. · Chem. Lett. · 1989 · 114510.1246/cl.1989.1145 ↗
20. Higuchi A. · Adv. Mater. · 1991 · 3 · 54910.1002/adma.19910031105 ↗
21. Inada H. · J. Mater. Chem. · 1993 · 3 · 31910.1039/jm9930300319 ↗
22. Kuwabara Y. · Adv. Mater. · 1994 · 6 · 67710.1002/adma.19940060913 ↗
23. Katsuma K. · Adv. Mater. · 1998 · 10 · 22310.1002/(SICI)1521-4095(199802)10:3<223::AID-ADMA223>3.0.CO;2-Q ↗
24. Wu I.-Y. · Adv. Mater. · 2000 · 12 · 66810.1002/(SICI)1521-4095(200005)12:9<668::AID-ADMA668>3.0.CO;2-G ↗
25. Noda T. · J. Mater. Chem. · 1999 · 9 · 217710.1039/a902800e ↗
26. Wang S. · J. Am. Chem. Soc. · 2000 · 122 · 569510.1021/ja992924w ↗
27. Kido J. · Science · 1995 · 67 · 133210.1126/science.267.5202.1332 ↗
28. Strukelj M. · J. Am. Chem. Soc. · 1996 · 118 · 121310.1021/ja953302n ↗
29. Shen Z. · Science · 1997 · 276 · 200910.1126/science.276.5321.2009 ↗
30. Leszthelyi C. P. · J. Electrochem. Soc. · 1973 · 120 · 24110.1149/1.2403427 ↗
31. Heller C. A. · J. Chem. Eng. Data · 1974 · 19 · 197410.1021/je60062a002 ↗
32. Collinson M. M. · Anal. Chem. · 1993 · 65 · 257710.1021/ac00067a006 ↗
33. Oyama M. · Anal. Chem. · 1998 · 70 · 507910.1021/ac980692y ↗
34. Boyd T. J. · Macromolecules · 1997 · 30 · 355310.1021/ma961613s ↗
35. Boyd T. J. · Macromolecules · 1999 · 32 · 660810.1021/ma990489k ↗
36. Adachi C. · Appl. Phys. Lett. · 1990 · 56 · 79910.1063/1.103177 ↗
37. Adams T. M. · Acta Crystallogr. B · 1979 · 35 · 67910.1107/S0567740879004428 ↗
38. Tamano M. · 1998
39. Shi J. · 1997
40. Sonsale A. Y. · Indian J. Chem. · 1976 · 14 · 408
41. Justin Thomas K. R. · Adv. Mater. · 2000 · 12 · 194910.1002/1521-4095(200012)12:24<1949::AID-ADMA1949>3.0.CO;2-X ↗
42. Justin Thomas K. R. · J. Am. Chem. Soc. · 2001 · 123 · 940410.1021/ja010819s ↗
43. Smet M. · Tetrahedron · 1999 · 55 · 785910.1016/S0040-4020(99)00406-8 ↗
44. Chen C. S. · J. Organomet. Chem. · 1981 · 215 · 28110.1016/S0022-328X(00)92605-6 ↗
45. Gilman H. · J. Am. Chem. Soc. · 1952 · 62 · 2332
46. Trepka W. J. · J. Organomet. Chem. · 1969 · 16 · 31710.1016/S0022-328X(00)81121-3 ↗
47. Cai D. · Tetrahedron Lett. · 1996 · 37 · 253710.1016/0040-4039(96)00336-X ↗
48. Nishiyama M. · Tetrahedron Lett · 1998 · 39 · 61710.1016/S0040-4039(97)10659-1 ↗
49. Hartwig J. F. · J. Org. Chem. · 1999 · 64 · 557510.1021/jo990408i ↗
50. Shirota Y. · J. Mater. Chem. · 2000 · 10 · 110.1039/a908130e ↗
51. Koene B. E. · Chem. Mater. · 1998 · 10 · 223510.1021/cm980186p ↗
52. Berlman I. B. Ed. · 1971
53. Turro N. J. · 1978
54. Workentin M. S. · J. Am. Chem. Soc. · 1994 · 116 · 827910.1021/ja00097a038 ↗
55. Pommerehne J. · Adv. Mater. · 1995 · 7 · 55110.1002/adma.19950070608 ↗
56. Thelakkat M. · Adv. Mater. · 1998 · 10 · 21910.1002/(SICI)1521-4095(199802)10:3<219::AID-ADMA219>3.0.CO;2-6 ↗