IP Library › Granted Patent US 12,336,427
Granted Patent B2
US 12,336,427 · App. 17/360,227 · Granted Jun 17, 2025

Organic electroluminescent materials and devices

Inventors: Chun Lin (Yardley, PA); Nicholas J. Thompson (New Hope, PA)
Assignee: UNIVERSAL DISPLAY CORPORATION
H10K85/6572H10K85/324H10K85/342H10K85/346H10K85/371H10K85/381H10K85/40H10K85/622H10K85/623H10K85/624H10K85/654H10K85/6574H10K85/6576H10K50/11H10K2101/10H10K2101/30H10K2101/90
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Quick Facts
Patent No.
US 12,336,427
App. No.
17/360,227
Granted
Jun 17, 2025
Kind
B2
Abstract

Provided is an OLED that includes, sequentially: an anode; a first emissive region; and a cathode; wherein the first emissive region comprises: a first compound; and a second compound; wherein the first compound is capable of functioning as a perovskite emitter in an OLED; wherein the second compound is capable of functioning as an emitter in an OLED, wherein the second compound is selected from the group consisting of phosphorescent emitters, fluorescent emitters, and delayed fluorescent emitters.

Claims (74)

1. An organic light emitting device (OLED) comprising, sequentially:

an anode;

a first emissive region; and

a cathode;

wherein the first emissive region comprises:

a first compound; and

a second compound;

wherein the first compound is a perovskite emitter that emits light from the OLED at room temperature;

wherein the second compound is capable of functioning as an emitter in an OLED at room temperature, wherein the second compound is selected from the group consisting of phosphorescent emitters, fluorescent emitters, and delayed fluorescent emitters, wherein the phosphorescent emitters are selected from metal coordination complexes where the metal M is Rh, Re, Ru, Os, Pt, Au, Ag, or Cu; and

wherein the first emissive region comprises a mixture of the first compound and the second compound.

2. The OLED of claim 1 , wherein the first emissive region comprises one or more layers; wherein each of the one or more layers comprises at least one of the first compound and the second compound.

3. The OLED of claim 1 , wherein the first emissive region emits light when a voltage is applied across the OLED, wherein emission energy of the second compound is higher than emission energy of the first compound; and excited states are transferred from the second compound to the first compound.

4. The OLED of claim 1 , wherein the OLED emits a luminescent emission comprising an emission component from both the first compound and the second compound when a voltage is applied across the OLED; wherein at least 30% of the emission spectrum of the second compound is overlapped with the absorption spectrum of the first compound.

5. The OLED of claim 1 , wherein the first compound is a perovskite compound having the formula of [A] a [B] b [X] c ;

wherein [A] is one or more types of organic cation or metal cation; [B] is one or more types of metal or metalloid cation; and [X] is one or more types of anions; a is an integer from 1 to 6; b is an integer from 1 to 6; and c is an integer from 1 to 21.

6. The OLED of claim 1 , wherein the second compound is capable of emitting light from a triplet excited state to a ground singlet state in the OLED at room temperature, wherein the second compound is a metal coordination complex having a metal-carbon bond or a metal-nitrogen bond, wherein the metal is selected from the group consisting of Rh, Re, Ru, Os, Pt, Au, Ag, and Cu.

7. The OLED of claim 1 , wherein the second compound comprises at least one donor group and at least one acceptor group; and

the second compound is a non-metal complex, or a Cu, Ag, or Au complex.

8. The OLED of claim 1 , wherein the second compound comprises at least one of the chemical moieties selected from the group consisting of:

wherein:

X is selected from the group consisting of O, S, Se, and NR;

each R can be same or different and is an acceptor group, or an organic linker bonded to an acceptor group, or a terminal group selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, aryl, heteroaryl, and combinations thereof; and

each R′ can be same or different and is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof.

9. The OLED of claim 1 , wherein the second compound comprises at least one organic group selected from the group consisting of:

and aza analogues thereof;

wherein A is selected from the group consisting of O, S, Se, NR′ and CR′R″;

wherein each R′ can be same or different and is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof.

10. The OLED of claim 1 , wherein the second compound is selected from the group consisting of:

wherein R 1 to R 5 each independently represents from mono to maximum number of substitutions they can have, or no substitution;

wherein R 1 to R 5 are each independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, selenyl, and combinations thereof.

11. The OLED of claim 1 , wherein the first emissive region further comprises a first host; wherein the first host has highest S 1 and T 1 energies among all materials in the first emissive region; and wherein the first and second compounds are dopants.

12. The OLED of claim 1 , wherein the first compound and the second compound each has an emission energy, and difference between the emission energy of the first compound and emission energy of the second compound is at least 0.25 eV.

13. The OLED of claim 1 , wherein at least one of the first compound and the second compound has photoluminescent quantum yield of at least 0.90.

14. The OLED of claim 1 , wherein the OLED further comprises a second emissive region deposited between the anode and the cathode; wherein the second emissive region comprises a phosphorescent emitting material.

15. An organic light emitting device (OLED) comprising, sequentially:

an anode;

a first emissive region; and

a cathode;

wherein the first emissive region comprises:

a first compound; and

a second compound;

wherein the first compound is capable of functioning as a perovskite emitter in an OLED at room temperature;

wherein the second compound is capable of functioning as an emitter in an OLED at room temperature, wherein the second compound has the formula of M(L 1 ) x (L 2 ) y (L 3 ) z ;

wherein,

metal M is Rh, Re, Ru, Os, Pt, Au, Ag, or Cu;

L 1 , L 2 and L 3 can be the same or different;

x is 1, 2, or 3;

y is 0, 1, or 2;

z is 0, 1, or 2;

x+y+z is the oxidation state of the metal M;

L 1 , L 2 and L 3 are each independently selected from the group consisting of:

wherein:

L 2 and L 3 can also be

each Y 1 to Y 13 are independently selected from the group consisting of carbon and nitrogen;

Y′ is selected from the group consisting of BR e , NR e , PR e , O, S, Se, C═O, S═O, SO 2 , CR e R f , SiR e R f , and GeR e R f ;

R e and R f can be fused or joined to form a ring;

each R a , R b , R c , and R d can independently represent from mono substitution to the maximum possible number of substitution, or no substitution;

each R a , R b , R c , R d , R e and R f is independently selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, selenyl, and combinations thereof; and

any two adjacent substituents of R a , R b , R c , and R d can be fused or joined to form a ring or form a multidentate ligand.

16. The OLED of claim 15 , wherein the first compound and the second compound are present as a mixture in the first emissive region.

17. The OLED of claim 15 , wherein the second compound is a phosphorescent emitter.

18. An organic light emitting device (OLED) comprising, sequentially:

an anode;

a first emissive region; and

a cathode;

wherein the first emissive region comprises:

a first compound; and

a second compound;

wherein the first compound is capable of functioning as a perovskite emitter in an OLED at room temperature;

wherein the second compound is capable of functioning as an emitter in an OLED at room temperature, wherein the second compound is selected from the group consisting of phosphorescent emitters, fluorescent emitters, and delayed fluorescent emitters, wherein the phosphorescent emitters are selected from metal coordination complexes where the metal M is Rh, Re, Ru, Os, Pt, Au, Ag, or Cu; and

wherein:

the first emissive region emits light when a voltage is applied across the OLED, wherein emission energy of the second compound is higher than emission energy of the first compound and excited states are trahsferred from the second compound to the first compound.

19. The OLED of claim 18 , wherein each of the first compound and the second compound are in separate layers within the first emissive region.

20. The OLED of claim 18 , wherein each of the first compound and the second compound are in separate layers within the first emissive region.

Assignments (1)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 28, 2021
From: LIN, CHUN; THOMPSON, NICHOLAS J.
To: UNIVERSAL DISPLAY CORPORATION
Reel/Frame 056687/0745 →
Continuity (2)
Provisional Application 63049901 · Jul 9, 2020
Related Publication 20220013731A1 · Jan 13, 2022
References Cited (195)
US 4769292A · Tang et al. · 1988 [cited by applicant]
US 5061569A · VanSlyke et al. · 1991 [cited by applicant]
US 5247190A · Friend et al. · 1993 [cited by applicant]
US 5703436A · Forrest et al. · 1997 [cited by applicant]
US 5707745A · Forrest et al. · 1998 [cited by applicant]
US 5834893A · Bulovic et al. · 1998 [cited by applicant]
US 5844363A · Gu et al. · 1998 [cited by applicant]
US 6013982A · Thompson et al. · 2000 [cited by applicant]
US 6087196A · Sturm et al. · 2000 [cited by applicant]
US 6091195A · Forrest et al. · 2000 [cited by applicant]
US 6097147A · Baldo et al. · 2000 [cited by applicant]
US 6294398B1 · Kim et al. · 2001 [cited by applicant]
US 6303238B1 · Thompson et al. · 2001 [cited by applicant]
US 6337102B1 · Forrest et al. · 2002 [cited by applicant]
US 6468819B1 · Kim et al. · 2002 [cited by applicant]
US 6528187B1 · Okada · 2003 [cited by applicant]
US 6687266B1 · Ma et al. · 2004 [cited by applicant]
US 6835469B2 · Kwong et al. · 2004 [cited by applicant]
US 6921915B2 · Takiguchi et al. · 2005 [cited by applicant]
US 7087321B2 · Kwong et al. · 2006 [cited by applicant]
US 7090928B2 · Thompson et al. · 2006 [cited by applicant]
US 7154114B2 · Brooks et al. · 2006 [cited by applicant]
US 7250226B2 · Tokito et al. · 2007 [cited by applicant]
US 7279704B2 · Walters et al. · 2007 [cited by applicant]
US 7332232B2 · Ma et al. · 2008 [cited by applicant]
US 7338722B2 · Thompson et al. · 2008 [cited by applicant]
US 7393599B2 · Thompson et al. · 2008 [cited by applicant]
US 7396598B2 · Takeuchi et al. · 2008 [cited by applicant]
US 7431968B1 · Shtein et al. · 2008 [cited by applicant]
US 7445855B2 · Mackenzie et al. · 2008 [cited by applicant]
US 7534505B2 · Lin et al. · 2009 [cited by applicant]
US 20020034656A1 · Thompson et al. · 2002 [cited by applicant]
US 20020134984A1 · Igarashi · 2002 [cited by applicant]
US 20020158242A1 · Son et al. · 2002 [cited by applicant]
US 20030138657A1 · Li et al. · 2003 [cited by applicant]
US 20030152802A1 · Tsuboyama et al. · 2003 [cited by applicant]
US 20030162053A1 · Marks et al. · 2003 [cited by applicant]
US 20030175553A1 · Thompson et al. · 2003 [cited by applicant]
US 20030230980A1 · Forrest et al. · 2003 [cited by applicant]
US 20040036077A1 · Ise · 2004 [cited by applicant]
US 20040137267A1 · Igarashi et al. · 2004 [cited by applicant]
US 20040137268A1 · Igarashi et al. · 2004 [cited by applicant]
US 20040174116A1 · Lu et al. · 2004 [cited by applicant]
US 20050025993A1 · Thompson et al. · 2005 [cited by applicant]
US 20050112407A1 · Ogasawara et al. · 2005 [cited by applicant]
US 20050238919A1 · Ogasawara · 2005 [cited by applicant]
US 20050244673A1 · Satoh et al. · 2005 [cited by applicant]
US 20050260441A1 · Thompson et al. · 2005 [cited by applicant]
US 20050260449A1 · Walters et al. · 2005 [cited by applicant]
US 20060008670A1 · Lin et al. · 2006 [cited by applicant]
US 20060202194A1 · Jeong et al. · 2006 [cited by applicant]
US 20060240279A1 · Adamovich et al. · 2006 [cited by applicant]
US 20060251923A1 · Lin et al. · 2006 [cited by applicant]
US 20060263635A1 · Ise · 2006 [cited by applicant]
US 20060280965A1 · Kwong et al. · 2006 [cited by applicant]
US 20070190359A1 · Knowles et al. · 2007 [cited by applicant]
US 20070278938A1 · Yabunouchi et al. · 2007 [cited by applicant]
US 20080015355A1 · Schafer et al. · 2008 [cited by applicant]
US 20080018221A1 · Egen et al. · 2008 [cited by applicant]
US 20080106190A1 · Yabunouchi et al. · 2008 [cited by applicant]
US 20080124572A1 · Mizuki et al. · 2008 [cited by applicant]
US 20080220265A1 · Xia et al. · 2008 [cited by applicant]
US 20080297033A1 · Knowles et al. · 2008 [cited by applicant]
US 20090008605A1 · Kawamura et al. · 2009 [cited by applicant]
US 20090009065A1 · Nishimura et al. · 2009 [cited by applicant]
US 20090017330A1 · Iwakuma et al. · 2009 [cited by applicant]
US 20090030202A1 · Iwakuma et al. · 2009 [cited by applicant]
US 20090039776A1 · Yamada et al. · 2009 [cited by applicant]
US 20090045730A1 · Nishimura et al. · 2009 [cited by applicant]
US 20090045731A1 · Nishimura et al. · 2009 [cited by applicant]
US 20090101870A1 · Prakash et al. · 2009 [cited by applicant]
US 20090108737A1 · Kwong et al. · 2009 [cited by applicant]
US 20090115316A1 · Zheng et al. · 2009 [cited by applicant]
US 20090165846A1 · Johannes et al. · 2009 [cited by applicant]
US 20090167162A1 · Lin et al. · 2009 [cited by applicant]
US 20090179554A1 · Kuma et al. · 2009 [cited by applicant]
US 20180090709A1 · Meng · 2018 [cited by examiner]
US 20180182977A1 · Hirose · 2018 [cited by examiner]
US 20200220094A1 · Matsushima · 2020 [cited by examiner]
US 20200287153A1 · Li · 2020 [cited by examiner]
US 20210130686A1 · Lim · 2021 [cited by examiner]
US 20210210707A1 · Levermore · 2021 [cited by examiner]
US 20210217996A1 · Hamilton · 2021 [cited by examiner]
US 20210305529A1 · Lee · 2021 [cited by examiner]
US 20220002618A1 · Li · 2022 [cited by examiner]
US 20220195290A1 · Aoki · 2022 [cited by examiner]
US 20220393128A1 · Lee · 2022 [cited by examiner]
CN 108735910A · 2018 [cited by examiner]
CN 108807704A · 2018 [cited by examiner]
EP 0650955 · 1995 [cited by applicant]
EP 1725079 · 2006 [cited by applicant]
EP 2034538 · 2009 [cited by applicant]
JP 200511610 · 2005 [cited by applicant]
JP 2007123392 · 2007 [cited by applicant]
JP 2007254297 · 2007 [cited by applicant]
JP 2008074939 · 2008 [cited by applicant]
KR 20200077201A · 2020 [cited by examiner]
WO 0139234 · 2001 [cited by applicant]
WO 0202714 · 2002 [cited by applicant]
WO 02015654 · 2002 [cited by applicant]
WO 03040257 · 2003 [cited by applicant]
WO 03060956 · 2003 [cited by applicant]
WO 2004093207 · 2004 [cited by applicant]
WO 2004107822 · 2004 [cited by applicant]
WO 2005014551 · 2005 [cited by applicant]
WO 2005019373 · 2005 [cited by applicant]
WO 2005030900 · 2005 [cited by applicant]
WO 2005089025 · 2005 [cited by applicant]
WO 2005123873 · 2005 [cited by applicant]
WO 2006009024 · 2006 [cited by applicant]
WO 2006056418 · 2006 [cited by applicant]
WO 2006072002 · 2006 [cited by applicant]
WO 2006082742 · 2006 [cited by applicant]
WO 2006098120 · 2006 [cited by applicant]
WO 2006100298 · 2006 [cited by applicant]
WO 2006103874 · 2006 [cited by applicant]
WO 2006114966 · 2006 [cited by applicant]
WO 2006132173 · 2006 [cited by applicant]
WO 2007002683 · 2007 [cited by applicant]
WO 2007004380 · 2007 [cited by applicant]
WO 2007063754 · 2007 [cited by applicant]
WO 2007063796 · 2007 [cited by applicant]
WO 2008056746 · 2008 [cited by applicant]
WO 2008101842 · 2008 [cited by applicant]
WO 2008132085 · 2008 [cited by applicant]
WO 2009000673 · 2008 [cited by applicant]
WO 2009003898 · 2009 [cited by applicant]
WO 2009008311 · 2009 [cited by applicant]
WO 2009018009 · 2009 [cited by applicant]
WO 2009021126 · 2009 [cited by applicant]
WO 2009050290 · 2009 [cited by applicant]
WO 2009062578 · 2009 [cited by applicant]
WO 2009063833 · 2009 [cited by applicant]
WO 2009066778 · 2009 [cited by applicant]
WO 2009066779 · 2009 [cited by applicant]
WO 2009086028 · 2009 [cited by applicant]
WO 2009100991 · 2009 [cited by applicant]
WO WO2019240545A1 · 2019 [cited by examiner]
Machine translation of WO-2019240545-A1, translation generated Mar. 2024, 25 pages. (Year: 2024). [cited by examiner]
Machine translation of CN-108807704-A, translation generated Mar. 2024, 9 pages. (Year: 2024). [cited by examiner]
Franz, Alexandra, et al. Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials 76.2 (2020): 267-274. (Year: 2020). [cited by examiner]
Passarelli, James V., et al. Journal of the American Chemical Society 140.23 (2018): 7313-7323. (Year: 2018). [cited by examiner]
Zhang, Xin, et al. The Journal of Physical Chemistry C 123.50 (2019): 30099-30105. (Year: 2019). [cited by examiner]
Matsushima, Toshinori, et al. Advanced Materials 30.38 (2018): 1802662. (Year: 2018). [cited by examiner]
Billing, David G. et al. CrystEngComm 9.3 (2007): 236-244. (Year: 2007). [cited by examiner]
Di Stasio, Francesco, et al. Chemistry of Materials 29.18 (2017): 7663-7667. (Year: 2017). [cited by examiner]
Machine translation of KR-20200077201-A, translation generated Mar. 2024, 18 pages. (Year: 2024). [cited by examiner]
Gao, Chun-Hong, et al. “84% efficiency improvement in all-inorganic perovskite light-emitting diodes assisted by a phosphorescent material.” RSC advances 8.28 (2018): 15698-15702. (Year: 2018). [cited by examiner]
Matsushima, Toshinori, et al. “Enhanced Electroluminescence from Organic Light-Emitting Diodes with an Organic-Inorganic Perovskite Host Layer.” Advanced Materials 30.38 (2018): 1802662. (Year: 2018). [cited by examiner]
Adachi, Chihaya et al., “Organic Electroluminescent Device Having a Hole Conductor as an Emitting Layer,” Appl. Phys. Lett., 55(15): 1489-1491 (1989). [cited by applicant]
Adachi, Chihaya et al., “Nearly 100% Internal Phosphorescence Efficiency in an Organic Light Emitting Device,” J. Appl. Phys., 90(10): 5048-5051 (2001). [cited by applicant]
Adachi, Chihaya et al., “High-Efficiency Red Electrophosphorescence Devices,” Appl. Phys. Lett., 78(11)1622-1624 (2001). [cited by applicant]
Aonuma, Masaki et al., “Material Design of Hole Transport Materials Capable of Thick-Film Formation in Organic Light Emitting Diodes,” Appl. Phys. Lett., 90, Apr. 30, 2007, 183503-1-183503-3. [cited by applicant]
Baldo et al., Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices, Nature, vol. 395, 151-154, (1998). [cited by applicant]
Baldo et al., Very high-efficiency green organic light-emitting devices based on electrophosphorescence, Appl. Phys. Lett., vol. 75, No. 1, 4-6 (1999). [cited by applicant]
Gao, Zhiqiang et al., “Bright-Blue Electroluminescence From a Silyl-Substituted ter-(phenylene-vinylene) derivative,” Appl. Phys. Lett., 74(6): 865-867 (1999). [cited by applicant]
Guo, Tzung-Fang et al., “Highly Efficient Electrophosphorescent Polymer Light-Emitting Devices,” Organic Electronics, 1: 15-20 (2000). [cited by applicant]
Hamada, Yuji et al., “High Luminance in Organic Electroluminescent Devices with Bis(10-hydroxybenzo[h]quinolinato) beryllium as an Emitter, ” Chem. Lett., 905-906 (1993). [cited by applicant]
Holmes, R.J. et al., “Blue Organic Electrophosphorescence Using Exothermic Host-Guest Energy Transfer,” Appl. Phys. Lett., 82(15):2422-2424 (2003). [cited by applicant]
Hu, Nan-Xing et al., “Novel High Tg Hole-Transport Molecules Based on Indolo[3,2-b]carbazoles for Organic Light-Emitting Devices,” Synthetic Metals, 111-112:421-424 (2000). [cited by applicant]
Huang, Jinsong et al., “Highly Efficient Red-Emission Polymer Phosphorescent Light-Emitting Diodes Based on Two Novel Tris(1-phenylisoquinolinato-C2, N)iridium(III) Derivatives,” Adv. Mater., 19:739-743 (2007). [cited by applicant]
Huang, Wei-Sheng et al., “Highly Phosphorescent Bis-Cyclometalated Iridium Complexes Containing Benzoimidazole-Based Ligands,” Chem. Mater., 16(12):2480-2488 (2004). [cited by applicant]
Hung, L.S. et al., “Anode Modification in Organic Light-Emitting Diodes by Low-Frequency Plasma Polymerization of CHF3,” Appl. Phys. Lett., 78(5):673-675 (2001). [cited by applicant]
Ikai, Masamichi et al., “Highly Efficient Phosphorescence From Organic Light-Emitting Devices with an Exciton-Block Layer,” Appl. Phys. Lett., 79(2):156-158 (2001). [cited by applicant]
Ikeda, Hisao et al., “P-185 Low-Drive-Voltage OLEDs with a Buffer Layer Having Molybdenum Oxide,” SID Symposium Digest, 37:923-926 (2006). [cited by applicant]
Inada, Hiroshi and Shirota, Yasuhiko, “1,3,5-Tris[4-(diphenylamino)phenyl]benzene and its Methylsubstituted Derivatives as a Novel Class of Amorphous Molecular Materials,” J. Mater. Chem., 3(3):319-320 (1993). [cited by applicant]
Kanno, Hiroshi et al., “Highly Efficient and Stable Red Phosphorescent Organic Light-Emitting Device Using bis [2-(2-benzothiazoyl)phenolato]zinc(II) as host material,” Appl. Phys. Lett., 90:123509-1-123509-3 (2007). [cited by applicant]
Kido, Junji et al., 1,2,4-Triazole Derivative as an Electron Transport Layer in Organic Electroluminescent Devices, Jpn. J. Appl. Phys., 32:L917-L920 (1993). [cited by applicant]
Kuwabara, Yoshiyuki et al., “Thermally Stable Multilayered Organic Electroluminescent Devices Using Novel Starburst Molecules, 4,4′,4″-Tri(N-carbazolyl)triphenylamine (TCTA) and 4,4′,4″-Tris(3-methylphenylphenyl-amino) … [cited by applicant]
Kwong, Raymond C. et al., “High Operational Stability of Electrophosphorescent Devices,” Appl. Phys. Lett., 81(1) 162-164 (2002). [cited by applicant]
Lamansky, Sergey et al., “Synthesis and Characterization of Phosphorescent Cyclometalated Iridium Complexes,” Inorg. Chem., 40(7):1704-1711 (2001). [cited by applicant]
Lee, Chang-Lyoul et al., “Polymer Phosphorescent Light-Emitting Devices Doped with Tris(2-phenylpyridine) Iridium as a Triplet Emitter,” Appl. Phys. Lett., 77(15):2280-2282 (2000). [cited by applicant]
Lo, Shih-Chun et al., “Blue Phosphorescence from Iridium(III) Complexes at Room Temperature,” Chem. Mater., 18 (21)5119-5129 (2006). [cited by applicant]
Ma, Yuguang et al., “Triplet Luminescent Dinuclear-Gold(I) Complex-Based Light-Emitting Diodes with Low Turn-On voltage,” Appl. Phys. Lett., 74(10): 1361-1363 (1999). [cited by applicant]
Mi, Bao-Xiu et al., “Thermally Stable Hole-Transporting Material for Organic Light-Emitting Diode an Isoindole Derivative,” Chem. Mater., 15(16):3148-3151 (2003). [cited by applicant]
Nishida, Jun-ichi et al., “Preparation, Characterization, and Electroluminescence Characteristics of α-Diimine-type Platinum(II) Complexes with Perfluorinated Phenyl Groups as Ligands,” Chem. Lett., 34(4): 592-593 (2005… [cited by applicant]
Niu, Yu-Hua et al., “Highly Efficient Electrophosphorescent Devices with Saturated Red Emission from a Neutral Osmium Complex,” Chem. Mater., 17(13):3532-3536 (2005). [cited by applicant]
Noda, Tetsuya and Shirota, Yasuhiko, “5,5′-Bis(dimesitylboryl)-2,2′-bithiophene and 5,5″-Bis(dimesitylboryl)-2,2′5′,2″-terthiophene as a Novel Family of Electron-Transporting Amorphous Molecular Materials,” J. Am. Chem.… [cited by applicant]
Okumoto, Kenji et al., “Green Fluorescent Organic Light-Emitting Device with External Quantum Efficiency of Nearly 10%,” Appl. Phys. Lett., 89:063504-1-063504-3 (2006). [cited by applicant]
Palilis, Leonidas C., “High Efficiency Molecular Organic Light-Emitting Diodes Based On Silole Derivatives And Their Exciplexes,” Organic Electronics, 4:113-121 (2003). [cited by applicant]
Paulose, Betty Marie Jennifer S. et al., “First Examples of Alkenyl Pyridines as Organic Ligands for Phosphorescent Iridium Complexes,” Adv. Mater., 16(22):2003-2007 (2004). [cited by applicant]
Ranjan, Sudhir et al., “Realizing Green Phosphorescent Light-Emitting Materials from Rhenium(I) Pyrazolato Diimine Complexes,” Inorg. Chem., 42(4):1248-1255 (2003). [cited by applicant]
Sakamoto, Youichi et al., “Synthesis, Characterization, and Electron-Transport Property of Perfluorinated Phenylene Dendrimers,” J. Am. Chem. Soc., 122(8):1832-1833 (2000). [cited by applicant]
Salbeck, J. et al., “Low Molecular Organic Glasses for Blue Electroluminescence,” Synthetic Metals, 91: 209-215 (1997). [cited by applicant]
Shirota, Yasuhiko et al., “Starburst Molecules Based on pi-Electron Systems as Materials for Organic Electroluminescent Devices,” Journal of Luminescence, 72-74:985-991 (1997). [cited by applicant]
Sotoyama, Wataru et al., “Efficient Organic Light-Emitting Diodes with Phosphorescent Platinum Complexes Containing N{circumflex over (0)}C{circumflex over (0)}N-Coordinating Tridentate Ligand,” Appl. Phys. Lett., 86:15… [cited by applicant]
Sun, Yiru and Forrest, Stephen R., “High-Efficiency White Organic Light Emitting Devices with Three Separate Phosphorescent Emission Layers,” Appl. Phys. Lett., 91:263503-1-263503-3 (2007). [cited by applicant]
T. östergård et al., “Langmuir-Blodgett Light-Emitting Diodes Of Poly(3-Hexylthiophene) Electro-Optical Characteristics Related to Structure,” Synthetic Metals, 88:171-177 (1997). [cited by applicant]
Takizawa, Shin-ya et al., “Phosphorescent Iridium Complexes Based on 2-Phenylimidazo[1,2- α]pyridine Ligands Tuning of Emission Color toward the Blue Region and Application to Polymer Light-Emitting Devices,” Inorg. Che… [cited by applicant]
Tang, C.W. and VanSlyke, S.A., “Organic Electroluminescent Diodes,” Appl. Phys. Lett., 51(12):913-915 (1987). [cited by applicant]
Tung, Yung-Liang et al., “Organic Light-Emitting Diodes Based on Charge-Neutral Ru II PHosphorescent Emitters,” Adv. Mater., 17(8)1059-1064 (2005). [cited by applicant]
Van Slyke, S. A. et al., “Organic Electroluminescent Devices with Improved Stability,” Appl. Phys. Lett., 69 (15):2160-2162 (1996). [cited by applicant]
Wang, Y. et al., “Highly Efficient Electroluminescent Materials Based on Fluorinated Organometallic Iridium Compounds,” Appl. Phys. Lett., 79(4):449-451 (2001). [cited by applicant]
Wong, Keith Man-Chung et al., A Novel Class of Phosphorescent Gold(III) Alkynyl-Based Organic Light-Emitting Devices with Tunable Colour, Chem. Commun., 2906-2908 (2005). [cited by applicant]
Wong, Wai-Yeung, “Multifunctional Iridium Complexes Based on Carbazole Modules as Highly Efficient Electrophosphors,” Angew. Chem. Int. Ed., 45:7800-7803 (2006). [cited by applicant]