journal article·2003-04-01

A New Family of Isophorone-Based Dopants for Red Organic Electroluminescent Devices

Jiuyan Li, Di Liu, Ziruo Hong, Shiwun Tong, Pengfei Wang, Chunwah Ma, Ondrej Lengyel, Chun-Sing Lee, Hoi-Lun Kwong, Shuittong Lee

Chemistry of Materials· Volume 15· Issue 7
Publisher page

Abstract

A new family of isophorone-based red fluorescent materials ( A, B, C, and D ) with a typical donor-π-acceptor structure was designed and synthesized for use in organic light-emitting devices (OLEDs). The asymmetrical π-conjugation structure of the isophorone skeleton facilitates the formation of highly pure products in comparison with the synthesis of pyran-containing DCM analogues. Saturated red-emitting devices with emission peaks at 640−680 nm were fabricated using these materials as dopants. The current efficiencies were moderately high and remained unchanged, even at high current density in some devices. The CIE coordinates of all the devices were comparable with or better than those of devices using DCM analogues.
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Research context

OpenAlex topics: Organic Light-Emitting Diodes Research · Organic Electronics and Photovoltaics · Conducting polymers and applications

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Affiliations

Center of Super-Diamond & Advanced Films (COSDAF), Department of Physics and Materials Sciences, and Department of Biology and Chemistry, City University of Hong Kong, Hong Kong SAR, China

References (23)

Show source-provided references
1. Tang C. W. · Appl. Phys. Lett. · 1987 · 51 · 91310.1063/1.98799 ↗
2. Burroughes J. H. · Nature · 1990 · 347 · 53910.1038/347539a0 ↗
3. Organic Electroluminescent Materials and Derivatives; Miyata, S., Nalwa, H. S., Eds.; Gordan and Breach: New York, 1997.
4. Hide F. · J. Acc. Chem. Res. · 1997 · 30 · 43010.1021/ar950191o ↗
5. Baldo M. A. · Appl. Phys. Lett. · 1999 · 75 · 410.1063/1.124258 ↗
6. Adachi C. · Appl. Phys. Lett. · 1990 · 57 · 53110.1063/1.103638 ↗
7. Yang Y. · J. Appl. Phys. · 1996 · 79 · 93410.1063/1.360875 ↗
8. Tao X. T. · J. Am. Chem. Soc. · 1999 · 121 · 944710.1021/ja9924142 ↗
9. Wu W. C. · Adv. Mater. · 2002 · 14 · 107210.1002/1521-4095(20020805)14:15<1072::AID-ADMA1072>3.0.CO;2-Z ↗
10. Tang C. W. · J. Appl. Phys. · 1989 · 65 · 361010.1063/1.343409 ↗
11. Chen C. H. · 1997
12. Tang C. W. · 1996
13. Burrows P. E. · Appl. Phys. Lett. · 1996 · 69 · 295910.1063/1.117743 ↗
14. Baldo M. A. · Nature · 1998 · 395 · 15110.1038/25954 ↗
15. Adachi C. · Appl. Phys. Lett. · 2001 · 78 · 162210.1063/1.1355007 ↗
16. Kido J. · Chem. Lett. · 1990 · 65710.1246/cl.1990.657 ↗
17. Kido J. · Appl. Phys. Lett. · 1994 · 65 · 212410.1063/1.112810 ↗
18. Adachi C. · J. Appl. Phys. · 2000 · 87 · 804910.1063/1.373496 ↗
19. Tao X. T. · Appl. Phys. Lett. · 2001 · 78 · 27910.1063/1.1341226 ↗
20. Lemke R. · Synthesis · 1974 · 35910.1055/s-1974-23322 ↗
21. Demas J. N. · J. Phys. Chem. · 1971 · 75 · 99110.1021/j100678a001 ↗
22. Young R. H. · Appl. Phys. Lett. · 2002 · 80 · 87410.1063/1.1445271 ↗
23. Hu W. P. · Appl. Phys. Lett. · 2000 · 77 · 427110.1063/1.1336161 ↗