US20060052641A1 - Material for organic electroluminescent device and organic electroluminescent device using same - Google Patents
Material for organic electroluminescent device and organic electroluminescent device using same Download PDFInfo
- Publication number
- US20060052641A1 US20060052641A1 US10/532,794 US53279405A US2006052641A1 US 20060052641 A1 US20060052641 A1 US 20060052641A1 US 53279405 A US53279405 A US 53279405A US 2006052641 A1 US2006052641 A1 US 2006052641A1
- Authority
- US
- United States
- Prior art keywords
- electroluminescent device
- light
- organic electroluminescent
- organic
- substituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- 0 CC(*)c(cc1)ccc1N(c1ccc(C(C)*)cc1)c1cc(c2ccccc2c(N(c2ccc(C(C)*)cc2)c2ccc(C(C)*)cc2)c2)c2c2c1cccc2 Chemical compound CC(*)c(cc1)ccc1N(c1ccc(C(C)*)cc1)c1cc(c2ccccc2c(N(c2ccc(C(C)*)cc2)c2ccc(C(C)*)cc2)c2)c2c2c1cccc2 0.000 description 4
- ZDCIKHODKQWXQU-UHFFFAOYSA-N C1=CC=C(C2=CC=C(C3=CC4=C(C=C(N(C5=CC=C(C6=CC=CC=C6)C=C5)C5=CC=C(C6=CC=CC=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C=C1.C1=CC=C(N(C2=CC=CC=C2)C2=CC=C(N(C3=CC=CC=C3)C3=CC=C(C4=CC5=C(C=C(C6=CC=C(N(C7=CC=CC=C7)C7=CC=C(N(C8=CC=CC=C8)C8=CC=CC=C8)C=C7)C=C6)C6=C5C=CC=C6)C5=CC=CC=C45)C=C3)C=C2)C=C1.CC1=CC=C(N(C2=CC=C(C)C=C2)C2=CC3=C(C=C(C4=CC=CC=C4)C4=CC=CC=C43)C3=C2C=CC=C3)C=C1 Chemical compound C1=CC=C(C2=CC=C(C3=CC4=C(C=C(N(C5=CC=C(C6=CC=CC=C6)C=C5)C5=CC=C(C6=CC=CC=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C=C1.C1=CC=C(N(C2=CC=CC=C2)C2=CC=C(N(C3=CC=CC=C3)C3=CC=C(C4=CC5=C(C=C(C6=CC=C(N(C7=CC=CC=C7)C7=CC=C(N(C8=CC=CC=C8)C8=CC=CC=C8)C=C7)C=C6)C6=C5C=CC=C6)C5=CC=CC=C45)C=C3)C=C2)C=C1.CC1=CC=C(N(C2=CC=C(C)C=C2)C2=CC3=C(C=C(C4=CC=CC=C4)C4=CC=CC=C43)C3=C2C=CC=C3)C=C1 ZDCIKHODKQWXQU-UHFFFAOYSA-N 0.000 description 1
- ZCYRABYPZLUXKS-UHFFFAOYSA-N C1=CC=C(N(C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C2=C3C=CC=CC3=C3C=CC=CC3=C2)C=C1.C1=CC=C(N(C2=CC=C(C3=CC4=C(C=C(C5=CC=C(N(C6=CC=CC=C6)C6=CC=C7C=CC=CC7=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C2=CC=C3C=CC=CC3=C2)C=C1.C1=CC=C(N(C2=CC=C3C=CC=CC3=C2)C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C=C1.CC1=CC=C(N(C2=CC=C(C)C=C2)C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C=C1.CC1=CC=C(N(C2=CC=C(C)C=C2)C2=CC=C(C3=CC4=C(C=C(C5=CC=C(N(C6=CC=C(C)C=C6)C6=CC=C(C)C=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C=C1.CC1=CC=C(N(C2=CC=CC=C2)C2=CC=C(C3=CC4=C(C=C(C5=CC=C(N(C6=CC=CC=C6)C6=CC=C(C)C=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C=C1.FC1=CC=C(N(C2=CC=C(F)C=C2)C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C=C1 Chemical compound C1=CC=C(N(C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C2=C3C=CC=CC3=C3C=CC=CC3=C2)C=C1.C1=CC=C(N(C2=CC=C(C3=CC4=C(C=C(C5=CC=C(N(C6=CC=CC=C6)C6=CC=C7C=CC=CC7=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C2=CC=C3C=CC=CC3=C2)C=C1.C1=CC=C(N(C2=CC=C3C=CC=CC3=C2)C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C=C1.CC1=CC=C(N(C2=CC=C(C)C=C2)C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C=C1.CC1=CC=C(N(C2=CC=C(C)C=C2)C2=CC=C(C3=CC4=C(C=C(C5=CC=C(N(C6=CC=C(C)C=C6)C6=CC=C(C)C=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C=C1.CC1=CC=C(N(C2=CC=CC=C2)C2=CC=C(C3=CC4=C(C=C(C5=CC=C(N(C6=CC=CC=C6)C6=CC=C(C)C=C6)C=C5)C5=C4C=CC=C5)C4=CC=CC=C34)C=C2)C=C1.FC1=CC=C(N(C2=CC=C(F)C=C2)C2=CC3=C(C=CC4=CC=CC=C43)C3=C2C=CC=C3)C=C1 ZCYRABYPZLUXKS-UHFFFAOYSA-N 0.000 description 1
- FYSCMYSZCIZQIY-UHFFFAOYSA-N c1ccc(cc(cc2)N(c3cc(cccc4)c4cc3)c3cc(c4ccccc4c(N(c4cc5ccccc5cc4)c4ccc(cccc5)c5c4)c4)c4c4c3cccc4)c2c1 Chemical compound c1ccc(cc(cc2)N(c3cc(cccc4)c4cc3)c3cc(c4ccccc4c(N(c4cc5ccccc5cc4)c4ccc(cccc5)c5c4)c4)c4c4c3cccc4)c2c1 FYSCMYSZCIZQIY-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
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- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
- Illuminated Signs And Luminous Advertising (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/711,655 US20070155991A1 (en) | 2002-11-12 | 2007-02-28 | Material for organic electroluminescent device and organic electroluminescent device using same |
US12/318,859 US8178218B2 (en) | 2002-11-12 | 2009-01-09 | Material for organic electroluminescent device and organic electroluminescent device using same |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002327956 | 2002-11-12 | ||
JP2002-327956 | 2002-11-12 | ||
PCT/JP2003/013366 WO2004044088A1 (fr) | 2002-11-12 | 2003-10-20 | Materiau pour dispositif electroluminescent organique, et dispositif electroluminescent organique utilisant ledit materiau |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/711,655 Continuation US20070155991A1 (en) | 2002-11-12 | 2007-02-28 | Material for organic electroluminescent device and organic electroluminescent device using same |
US12/318,859 Continuation US8178218B2 (en) | 2002-11-12 | 2009-01-09 | Material for organic electroluminescent device and organic electroluminescent device using same |
Publications (1)
Publication Number | Publication Date |
---|---|
US20060052641A1 true US20060052641A1 (en) | 2006-03-09 |
Family
ID=32310532
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/532,794 Abandoned US20060052641A1 (en) | 2002-11-12 | 2003-10-20 | Material for organic electroluminescent device and organic electroluminescent device using same |
US11/711,655 Abandoned US20070155991A1 (en) | 2002-11-12 | 2007-02-28 | Material for organic electroluminescent device and organic electroluminescent device using same |
US12/318,859 Expired - Lifetime US8178218B2 (en) | 2002-11-12 | 2009-01-09 | Material for organic electroluminescent device and organic electroluminescent device using same |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/711,655 Abandoned US20070155991A1 (en) | 2002-11-12 | 2007-02-28 | Material for organic electroluminescent device and organic electroluminescent device using same |
US12/318,859 Expired - Lifetime US8178218B2 (en) | 2002-11-12 | 2009-01-09 | Material for organic electroluminescent device and organic electroluminescent device using same |
Country Status (9)
Country | Link |
---|---|
US (3) | US20060052641A1 (fr) |
EP (1) | EP1561794B1 (fr) |
JP (1) | JP4205059B2 (fr) |
KR (1) | KR101031719B1 (fr) |
CN (2) | CN1978586A (fr) |
AT (1) | ATE472585T1 (fr) |
DE (1) | DE60333214D1 (fr) |
TW (1) | TW200420709A (fr) |
WO (1) | WO2004044088A1 (fr) |
Cited By (48)
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US20060110867A1 (en) * | 2004-11-10 | 2006-05-25 | Canon Kabushiki Kaisha | Field effect transistor manufacturing method |
US20060189828A1 (en) * | 1998-12-28 | 2006-08-24 | Idemitsu Kosan Co., Ltd. | Organic electrolumescence device |
US20060194074A1 (en) * | 2005-02-07 | 2006-08-31 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescence device using the same |
US20060210830A1 (en) * | 2005-03-15 | 2006-09-21 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescence device using the same |
US20070236137A1 (en) * | 2006-03-03 | 2007-10-11 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescence device using the same |
US20070291202A1 (en) * | 2006-06-16 | 2007-12-20 | Tsuyoshi Sasaki | Reflective liquid crystal display |
US20080268285A1 (en) * | 2007-04-27 | 2008-10-30 | Canon Kabushiki Kaisha | Organic electroluminescent device |
US20080303430A1 (en) * | 2007-06-01 | 2008-12-11 | Norman Herron | Blue luminescent materials |
US20080303428A1 (en) * | 2007-06-01 | 2008-12-11 | Vsevolod Rostovtsev | Chrysenes for green luminescent applications |
US20080306303A1 (en) * | 2007-06-01 | 2008-12-11 | Vsevolod Rostovtsev | Chrysenes for deep blue luminescent applications |
US20090162693A1 (en) * | 2006-12-28 | 2009-06-25 | Alex Sergey Ionkin | Tetra-substituted chrysenes for luminescent applications |
US20100156285A1 (en) * | 2007-06-18 | 2010-06-24 | Idemitsu Kosan Co., Ltd. | Trinaphthyl monoamine or derivative thereof, organic electroluminescent device using the same, and organic electroluminescent material-containing solution |
WO2010059837A3 (fr) * | 2008-11-19 | 2010-07-22 | E. I. Du Pont De Nemours And Company | Composés de chrysène pour des applications de luminescence bleue ou verte |
US20100187981A1 (en) * | 2008-12-19 | 2010-07-29 | E. I. Du Pont De Nemours And Company | Chrysene derivative host materials |
US20100186806A1 (en) * | 2009-01-26 | 2010-07-29 | Mitsubishi Electric Corporation | Photovoltaic module |
US20100187983A1 (en) * | 2008-12-22 | 2010-07-29 | E. I. Du Pont De Nemours And Company | Deuterated compounds for luminescent applications |
US20100244665A1 (en) * | 2008-01-11 | 2010-09-30 | E. I. Du Pont De Nemours And Company | Substituted pyrenes and associated production methods for luminescent applications |
US20110006289A1 (en) * | 2007-12-28 | 2011-01-13 | Idemitsu Kosan Co., Ltd. | Aromatic diamine derivative and organic electroluminescent device using the same |
US20110017980A1 (en) * | 2009-07-27 | 2011-01-27 | E. I. Du Pont De Nemours And Company | Process and materials for making contained layers and devices made with same |
US20110037056A1 (en) * | 2008-12-12 | 2011-02-17 | E. I. Du Pont De Nemours And Company | Photoactive composition and electronic device made with the composition |
US20110037057A1 (en) * | 2009-02-27 | 2011-02-17 | E.I. Du Pont De Nemours And Company | Deuterated compounds for electronic applications |
WO2011019360A1 (fr) * | 2009-08-13 | 2011-02-17 | E. I. Du Pont De Nemours And Company | Matériaux dérivés du chrysène |
US20110057173A1 (en) * | 2009-02-27 | 2011-03-10 | E. I. Du Pont De Nemours And Company | Deuterated compounds for electronic applications |
US20110095273A1 (en) * | 2009-09-29 | 2011-04-28 | E. I. Du Pont De Nemours And Company | Deuterated compounds for luminescent applications |
WO2011002870A3 (fr) * | 2009-07-01 | 2011-05-05 | E. I. Du Pont De Nemours And Company | Composés de chrysène pour applications luminescentes |
US20110101312A1 (en) * | 2009-10-29 | 2011-05-05 | E. I. Du Pont De Nemours And Company | Deuterated compounds for electronic applications |
US20110121269A1 (en) * | 2009-05-19 | 2011-05-26 | E.I. Du Pont De Nemours And Company | Deuterated compounds for electronic applications |
US20110133632A1 (en) * | 2009-12-09 | 2011-06-09 | E.I. Du Pont De Nemours And Company | Deuterated compound as part of a combination of compounds for electronic applications |
US8257836B2 (en) | 2006-12-29 | 2012-09-04 | E I Du Pont De Nemours And Company | Di-substituted pyrenes for luminescent applications |
US8263973B2 (en) | 2008-12-19 | 2012-09-11 | E I Du Pont De Nemours And Company | Anthracene compounds for luminescent applications |
US8273468B2 (en) | 2007-06-01 | 2012-09-25 | E I Du Pont De Nemours And Company | Green luminescent materials |
US8497495B2 (en) | 2009-04-03 | 2013-07-30 | E I Du Pont De Nemours And Company | Electroactive materials |
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US8648333B2 (en) | 2009-10-19 | 2014-02-11 | E I Du Pont De Nemours And Company | Triarylamine compounds for use in organic light-emitting diodes |
US20140103319A1 (en) * | 2008-03-19 | 2014-04-17 | Idemitsu Kosan Co., Ltd. | Anthracene derivatives, luminescent materials and organic electroluminescent devices |
US8937300B2 (en) | 2009-10-19 | 2015-01-20 | E I Du Pont De Nemours And Company | Triarylamine compounds for use in organic light-emitting diodes |
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Also Published As
Publication number | Publication date |
---|---|
EP1561794A4 (fr) | 2008-08-20 |
US20070155991A1 (en) | 2007-07-05 |
ATE472585T1 (de) | 2010-07-15 |
EP1561794B1 (fr) | 2010-06-30 |
DE60333214D1 (de) | 2010-08-12 |
US20090195149A1 (en) | 2009-08-06 |
US8178218B2 (en) | 2012-05-15 |
JPWO2004044088A1 (ja) | 2006-03-09 |
TW200420709A (en) | 2004-10-16 |
EP1561794A1 (fr) | 2005-08-10 |
WO2004044088A1 (fr) | 2004-05-27 |
CN1711334A (zh) | 2005-12-21 |
JP4205059B2 (ja) | 2009-01-07 |
KR101031719B1 (ko) | 2011-04-29 |
CN1978586A (zh) | 2007-06-13 |
CN100343359C (zh) | 2007-10-17 |
TWI327159B (fr) | 2010-07-11 |
KR20050086518A (ko) | 2005-08-30 |
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