Stock material or miscellaneous articles – Composite – Of inorganic material
Reexamination Certificate
2006-10-25
2009-10-20
Tarazano, D. Lawrence (Department: 1794)
Stock material or miscellaneous articles
Composite
Of inorganic material
C428S917000, C313S504000, C313S506000, C252S301160, C252S500000
Reexamination Certificate
active
07604874
ABSTRACT:
Disclosed is a novel group of compounds having a general structure of anthracene body substituted with at least one thiophenyl group, which can be further substituted with various substituent groups. These new compounds are generally compatible with organic electroluminescence. Also disclosed are organic electroluminescent devices and method of making the same. The organic electroluminescent devices include at least one of the compounds in various layers thereof. Organic electroluminescent devices employing the new compounds in their light-emitting layers show outstanding stability.
REFERENCES:
patent: 4356429 (1982-10-01), Tang et al.
patent: 4720432 (1988-01-01), VanSlyke et al.
patent: 4736032 (1988-04-01), Fox et al.
patent: 5026894 (1991-06-01), Tour et al.
patent: 5059863 (1991-10-01), Tashiro et al.
patent: 5061569 (1991-10-01), VanSlyke et al.
patent: 5227252 (1993-07-01), Murayama et al.
patent: 5256945 (1993-10-01), Imai et al.
patent: 5432014 (1995-07-01), Sano et al.
patent: 5516577 (1996-05-01), Matsuura et al.
patent: 5540999 (1996-07-01), Yamamoto et al.
patent: 5609970 (1997-03-01), Kolb et al.
patent: 5811833 (1998-09-01), Thompson
patent: 5817431 (1998-10-01), Shi et al.
patent: 5840217 (1998-11-01), Lupo et al.
patent: 5998803 (1999-12-01), Forrest et al.
patent: 6020078 (2000-02-01), Chen et al.
patent: 6074734 (2000-06-01), Kawamura et al.
patent: 6312836 (2001-11-01), Bulovic et al.
patent: 6355365 (2002-03-01), Hotta et al.
patent: 6361886 (2002-03-01), Shi et al.
patent: 6383666 (2002-05-01), Kim et al.
patent: 6458475 (2002-10-01), Adachi et al.
patent: 2002/0048687 (2002-04-01), Hosokawa et al.
patent: 2002/0048887 (2002-04-01), Hwang et al.
patent: 0 926 216 (1999-06-01), None
patent: 1-087-066 (2001-03-01), None
patent: 1 182 183 (2002-02-01), None
patent: 1 645 552 (2006-04-01), None
patent: 05-202356 (1993-08-01), None
patent: 06-240243 (1994-08-01), None
patent: 06-306357 (1994-11-01), None
patent: 6-306357 (1994-11-01), None
patent: 07-166160 (1995-06-01), None
patent: 1996-269445 (1996-10-01), None
patent: 09-199276 (1997-07-01), None
patent: 1998-017860 (1998-01-01), None
patent: 11-067449 (1999-03-01), None
patent: 11-111460 (1999-04-01), None
patent: 11-219788 (1999-08-01), None
patent: 11-233263 (1999-08-01), None
patent: 00-058267 (2000-02-01), None
patent: 2000-053676 (2000-02-01), None
patent: 06-009952 (2000-03-01), None
patent: 2000-182772 (2000-06-01), None
patent: 2000-515926 (2000-11-01), None
patent: 2001-076879 (2001-03-01), None
patent: 2001-123157 (2001-05-01), None
patent: 2002-059676 (2002-02-01), None
patent: 2002-060742 (2002-02-01), None
patent: 3971310 (2007-06-01), None
patent: WO 00/58315 (2000-10-01), None
patent: WO 01/72673 (2001-10-01), None
patent: WO 02/088274 (2002-11-01), None
Hamada, et al. Organic light-emitting diodes using a gallium complex., Apr. 20, 1998, American Institute of Physics, vol. 72, No. 16.
Murata, et al. Organic light-emitting devices with saturated red emission using 6, 13-dephenylpentacene., Apr. 16, 2001, American Institute of Physics, vol. 78, No. 16.
Shi, et al. Doped organic electroluminescent devices with improved stability., Mar. 31 1997, American Institute of Physics, vol. 70, No. 13.
Adachi, et al., High-efficiency organic electrophosphorescent devices with tris (2-phenypyridine) iridium doped into electron-transporting materials., Aug. 7, 2000, American Institute of Physics, vol. 77, No. 6.
Adachi, et al. High efficiency red electrophosphorescence devices., Mar. 12, 2001, American Institute of Physics, vol. 78, No. 11.
Burrows et al. Operating lifetime of phosphorescent organic light emitting., May 1, 2000, American Institute of Physics., vol. 76, No. 18.
Baldo et al. Very high-efficiency green organic light-emitting devices based on electrophosphorescene., Jul. 5, 1999, American Institute of Physics., vol. 75, No. 1.
Baldo, et al. Improved energy transfer in electrophosphorescent devices., Jan. 18, 1999, American Institute of Physics., vol. 74, No. 3.
Hamada, et al. Organic light-emitting diodes using 3-or 5-hydroxyflavone-metal complexes., Dec. 8, 1997, American Institute of Physics., vol. 71, No. 23.
Gigli, et al. High-efficiency oligothiopene-based light-emitting diodes., Jul. 26, 1999, American Institute of Physics., vol. 75, No. 4.
Kido et al. Fabrication of highly efficient organic electroluminescent devices., Nov. 9, 1998, American Institute of Physic., vol. 75, No. 4.
Yang, et al. Photoluminescence and electroluminescence properties of dye-doped polymer system., 1997, Elsevier Science S.A., Synthetic Metals., 335-336.
Watanabe et al. Optimization of emitting efficiency in organic LEDs., 1997 Elsevier Science S.A., Synthetic Metals., 203-207.
Liedenbaum., Low voltage of large area polymer LEDs., 1997, Elsevier Science S.A. Synthetic Metals., 109-111.
Hide, et al. Conjugated Polymers as solid-state laser materials., 1997, Elsevier Science S.A., Synthetic Metals., 35-40.
Muckl ,et al. Transient electroluminescence measurements on organic heterolayer light emitting diodes., 2000 Elsevier Science S.A. Synthetic Metals., 91-94.
Baldo, et al. Nature, High-efficiency florescent organic light-emitting devices using a phosphorescent sensitizer, 2000, vol. 402,750-753.
Birnstock, et al., Applied Physics Letters, Screen-printed passive matrix displays based on light-emitting polymers, vol. 78, No. 24., Jun. 2001, 3905-3907.
Chang, et al. Dual-color polymer light-emitting pixels processed by hybrid inkjet printing, Nov. 1989, vol. 73, No. 18, 2561-2563, Applied Physics Letters, 78, 24, 2001, 3905- 3907.
Wurther et al., Synthesis and Energy Transfer Properties of Terminally Substituted Oligothiophenes, Feb. 1995, American Chemical Society, pp. 8090-8099.
Shoustikov et al., Orange and red organic light-emitting devices using aluminum tris(5-hydroxyquinoxaline), 1997, Elsevier Science S.A., Sythetic Metals., 217-221.
Tokito et al., strongly modified emission from organic elelctroluminescent device with a microcavity., 1997. Elsevier Science S.A. Sythetic Metals., 49-52.
Wakimoto et al., Stability characteristics of quinacridone and coumarin molecules as guest dopants in the organic LEDs., 1997, Elsevier Science S.A., Sythetic Metals., 15-19.
Ma et al., Bright blue electroluminescent devices utiliaing poly (N—vinylcarbazole) doped with fluorescent dye., 1997, Elsevier Science S.A., Sythetic Metals., 331-332.
Sano et al., Organic eletroluminescent devices doped condensed polycyclic aromatic compounds., 1997, Elsevier Science S.A., Sythetic Metals., 27-30.
Mitschke et al., The electroluminescence of organic materials., 2000, The Royal Society of Chemistry, 1471-1507.
Barbarella et al., Modified Oligothiophenes with High Photo and Electroluminescence Efficiencies., 1999, Advanced Materals, 11, No. 16.
Schmitz et al., Polymeric Light-Emitting Diodes Based on Poly(p-phenylene ethynylene), Poly(triphenyldiamine), and Spiroquinoxaline., 2001, Advanced Functional Materials, 11, No. 1.
Lamansky et al., Synthesis and Characterization of Phosphorescent Cyclometalated Iridium Complexes., 2001. Dept. of Chemistry. University of Southern California, 1704-1711.
Lamansky et al., Highly Phosphorescent Bis-Cyclometalated Iridium Complexes: Synthesis, Photophysical Characterization, and Use in Organic Light Emitting Diodes., 2001, American Chemical Society, 123, 4304-4312.
Tsutsui et al., High Quantum Efficiency in Organic Light-Emitting Devices with Iridium-Complex as a Triplet Emissive Center., 1999, Japanese Journal fo Applied Physics., vol. 38, L1502-L1504.
Naito et al., Molecular Design for Nonpolymeric Organic Dye Glasses with Thermal Stability Relations between Thermodynamic Parameters and Amorphous Properties., 1993, The Journal of Physical Chemistry, vol. 97, No. 23, 6240-6248.
Barth et al., Electron mobility in tris(8-hydroxy-quinoline)aluminum thin filims determined via transient eletroluminescence from single- and multilayer organic light-emitting diodes., Apr. 1, 2001, Journal of Applied Physics, vol. 89, No. 7, 3711-3719.
Adachi et al., Organic electroluminescence of silole-incorporated p
Bae Jae-Soon
Im Sung-Gap
Jang Jun-Gi
Kim Ji-Eun
Kim Kong-Kyeum
LG Chem Ltd.
McKenna Long & Aldridge LLP
Tarazano D. Lawrence
Thompson Camie S
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