KR101670036B1 - 벤조옥사졸 유도체, 벤조옥사졸 유도체를 이용한 발광소자, 발광장치 및 전자기기 - Google Patents
벤조옥사졸 유도체, 벤조옥사졸 유도체를 이용한 발광소자, 발광장치 및 전자기기 Download PDFInfo
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- KR101670036B1 KR101670036B1 KR1020090082580A KR20090082580A KR101670036B1 KR 101670036 B1 KR101670036 B1 KR 101670036B1 KR 1020090082580 A KR1020090082580 A KR 1020090082580A KR 20090082580 A KR20090082580 A KR 20090082580A KR 101670036 B1 KR101670036 B1 KR 101670036B1
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- FUESUFHXMQBDPR-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c1nc2ccccc2[o]1 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c1nc2ccccc2[o]1 FUESUFHXMQBDPR-UHFFFAOYSA-N 0.000 description 2
- AFPUAZLMDWRPRP-UHFFFAOYSA-N Brc1c2[o]c(-c(cc3)ccc3-c(cc3)ccc3-[n]3c(cccc4)c4c4ccccc34)nc2ccc1 Chemical compound Brc1c2[o]c(-c(cc3)ccc3-c(cc3)ccc3-[n]3c(cccc4)c4c4ccccc34)nc2ccc1 AFPUAZLMDWRPRP-UHFFFAOYSA-N 0.000 description 1
- PHXZVFJUZXATKP-UHFFFAOYSA-N CC(C)(C)c1c2[o]c(-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)nc2cc(C)c1 Chemical compound CC(C)(C)c1c2[o]c(-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)nc2cc(C)c1 PHXZVFJUZXATKP-UHFFFAOYSA-N 0.000 description 1
- HOPOKFSOWHCUQR-UHFFFAOYSA-N CC1(C)c(cc(cc2)-c(cc3)cc(c4cc(-c5nc6ccccc6[o]5)ccc44)c3[n]4-c3ccccc3)c2-c2ccccc12 Chemical compound CC1(C)c(cc(cc2)-c(cc3)cc(c4cc(-c5nc6ccccc6[o]5)ccc44)c3[n]4-c3ccccc3)c2-c2ccccc12 HOPOKFSOWHCUQR-UHFFFAOYSA-N 0.000 description 1
- OGFQCENOEKHTCS-UHFFFAOYSA-N CCC(C)c1cc(C)c2[o]c(-c(cc3)ccc3-[n]3c(cccc4)c4c4ccccc34)nc2c1 Chemical compound CCC(C)c1cc(C)c2[o]c(-c(cc3)ccc3-[n]3c(cccc4)c4c4ccccc34)nc2c1 OGFQCENOEKHTCS-UHFFFAOYSA-N 0.000 description 1
- IWTNSAXRTCRHGT-UHFFFAOYSA-N CCCCc1ccc2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 Chemical compound CCCCc1ccc2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 IWTNSAXRTCRHGT-UHFFFAOYSA-N 0.000 description 1
- JROHFNLCGAZOIL-UHFFFAOYSA-N CCCc1cc(C)cc2c1[o]c(-c(cc1)ccc1-[n]1c(cccc3)c3c3c1cccc3)n2 Chemical compound CCCc1cc(C)cc2c1[o]c(-c(cc1)ccc1-[n]1c(cccc3)c3c3c1cccc3)n2 JROHFNLCGAZOIL-UHFFFAOYSA-N 0.000 description 1
- WWYMFZLWIDQPKE-UHFFFAOYSA-N CCCc1ccc2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 Chemical compound CCCc1ccc2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 WWYMFZLWIDQPKE-UHFFFAOYSA-N 0.000 description 1
- JWUMJLYMIPHXKB-UHFFFAOYSA-N CCc1c2[o]c(-c(cc3)ccc3-[n]3c(cccc4)c4c4ccccc34)nc2cc(C)c1 Chemical compound CCc1c2[o]c(-c(cc3)ccc3-[n]3c(cccc4)c4c4ccccc34)nc2cc(C)c1 JWUMJLYMIPHXKB-UHFFFAOYSA-N 0.000 description 1
- AZWMULPMEARXSR-UHFFFAOYSA-N CCc1cc(C)c2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 Chemical compound CCc1cc(C)c2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 AZWMULPMEARXSR-UHFFFAOYSA-N 0.000 description 1
- HCYNMDKCYOPGEK-UHFFFAOYSA-N CCc1cc(CC)c2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 Chemical compound CCc1cc(CC)c2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 HCYNMDKCYOPGEK-UHFFFAOYSA-N 0.000 description 1
- UQLOCWJHLVWRBM-UHFFFAOYSA-N Cc1ccc2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 Chemical compound Cc1ccc2[o]c(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)nc2c1 UQLOCWJHLVWRBM-UHFFFAOYSA-N 0.000 description 1
- DYBVGECZURTERP-UHFFFAOYSA-N Clc1cccc2c1[o]c(-c(cc1)ccc1-c(cc1)ccc1-[n]1c(cccc3)c3c3ccccc13)n2 Chemical compound Clc1cccc2c1[o]c(-c(cc1)ccc1-c(cc1)ccc1-[n]1c(cccc3)c3c3ccccc13)n2 DYBVGECZURTERP-UHFFFAOYSA-N 0.000 description 1
- RPROVVYBCHEIIV-UHFFFAOYSA-N Fc1c2[o]c(-c(cc3)ccc3-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)nc2ccc1 Chemical compound Fc1c2[o]c(-c(cc3)ccc3-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)nc2ccc1 RPROVVYBCHEIIV-UHFFFAOYSA-N 0.000 description 1
- ARWHANYRTWSTFT-UHFFFAOYSA-N Ic1c2[o]c(-c(cc3)ccc3-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)nc2ccc1 Chemical compound Ic1c2[o]c(-c(cc3)ccc3-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)nc2ccc1 ARWHANYRTWSTFT-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N Nc1ccccc1O Chemical compound Nc1ccccc1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- NJAKCIUOTIPYED-UHFFFAOYSA-N O=C(c(cc1)ccc1I)Cl Chemical compound O=C(c(cc1)ccc1I)Cl NJAKCIUOTIPYED-UHFFFAOYSA-N 0.000 description 1
- XRWYJWAGOCHWKQ-UHFFFAOYSA-N Oc1ccccc1NC(c(cc1)ccc1I)=O Chemical compound Oc1ccccc1NC(c(cc1)ccc1I)=O XRWYJWAGOCHWKQ-UHFFFAOYSA-N 0.000 description 1
- FVIMUYIBTRFNME-UHFFFAOYSA-N c(cc1)cc(c2cc(-c3nc4ccccc4[o]3)ccc22)c1[n]2-c(cc1)ccc1-c1cccc2c1cccc2 Chemical compound c(cc1)cc(c2cc(-c3nc4ccccc4[o]3)ccc22)c1[n]2-c(cc1)ccc1-c1cccc2c1cccc2 FVIMUYIBTRFNME-UHFFFAOYSA-N 0.000 description 1
- VHAOFJVODLESQS-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c([o]c1ccc2)nc1c2-c1cc2ccccc2cc1 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c([o]c1ccc2)nc1c2-c1cc2ccccc2cc1 VHAOFJVODLESQS-UHFFFAOYSA-N 0.000 description 1
- CQCPIARNQJHAGF-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c([o]c1ccc2)nc1c2-c1cccc2c1cccc2 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c([o]c1ccc2)nc1c2-c1cccc2c1cccc2 CQCPIARNQJHAGF-UHFFFAOYSA-N 0.000 description 1
- MLAMMKIKBLDRAB-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c1nc(ccc(-c(cc2)cc3c2c(-c(cc2)cc(c4ccccc44)c2[n]4-c(cc2)ccc2-c(cc2)ccc2-c([o]c2c4)nc2ccc4-c2cccc4c2cccc4)ccc3)c2)c2[o]1 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c1nc(ccc(-c(cc2)cc3c2c(-c(cc2)cc(c4ccccc44)c2[n]4-c(cc2)ccc2-c(cc2)ccc2-c([o]c2c4)nc2ccc4-c2cccc4c2cccc4)ccc3)c2)c2[o]1 MLAMMKIKBLDRAB-UHFFFAOYSA-N 0.000 description 1
- JCUIYUDGCCYOQX-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c1nc(cccc2-c3ccc(cccc4)c4c3)c2[o]1 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c1nc(cccc2-c3ccc(cccc4)c4c3)c2[o]1 JCUIYUDGCCYOQX-UHFFFAOYSA-N 0.000 description 1
- KMAMQQKSELODOM-UHFFFAOYSA-N c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c1nc(cccc2-c3cccc4ccccc34)c2[o]1 Chemical compound c(cc1)cc(c2ccccc22)c1[n]2-c(cc1)ccc1-c(cc1)ccc1-c1nc(cccc2-c3cccc4ccccc34)c2[o]1 KMAMQQKSELODOM-UHFFFAOYSA-N 0.000 description 1
- ZGNIOUUOSBKGFW-UHFFFAOYSA-N c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c(cc1)ccc1-c(cc1)ccc1-c1nc2cc(-c(cc3)ccc3-c(cc3)ccc3-[n](c(cccc3)c3c3c4)c3ccc4-c(cc3)ccc3-c(cc3)ccc3-c3nc4ccccc4[o]3)ccc2[o]1 Chemical compound c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c(cc1)ccc1-c(cc1)ccc1-c1nc2cc(-c(cc3)ccc3-c(cc3)ccc3-[n](c(cccc3)c3c3c4)c3ccc4-c(cc3)ccc3-c(cc3)ccc3-c3nc4ccccc4[o]3)ccc2[o]1 ZGNIOUUOSBKGFW-UHFFFAOYSA-N 0.000 description 1
- HMXPJCMACNPZBW-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c(cc2)ccc2-c2cccc3c2cccc3)c2)c2c2cc(-c3nc4ccccc4[o]3)ccc12 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c(cc2)ccc2-c2cccc3c2cccc3)c2)c2c2cc(-c3nc4ccccc4[o]3)ccc12 HMXPJCMACNPZBW-UHFFFAOYSA-N 0.000 description 1
- LWNSQBRULXRTEB-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c(cc2C34c5ccccc5-c5ccccc35)ccc2-c2c4cccc2)c2)c2c2c1ccc(-c1nc3ccccc3[o]1)c2 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c(cc2C34c5ccccc5-c5ccccc35)ccc2-c2c4cccc2)c2)c2c2c1ccc(-c1nc3ccccc3[o]1)c2 LWNSQBRULXRTEB-UHFFFAOYSA-N 0.000 description 1
- FWYYWCBYZMZWSX-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1nc(cccc2)c2[o]1 Chemical compound c(cc1)ccc1-c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1nc(cccc2)c2[o]1 FWYYWCBYZMZWSX-UHFFFAOYSA-N 0.000 description 1
- DHDHJYNTEFLIHY-UHFFFAOYSA-N c(cc1)ccc1-c1c(ccc2c3nccc2-c2ccccc2)c3ncc1 Chemical compound c(cc1)ccc1-c1c(ccc2c3nccc2-c2ccccc2)c3ncc1 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 1
- XSTDSKHANUJGJF-UHFFFAOYSA-N c1ccc(C2(c(cc(cc3)-c(cc4)cc(c5cc(-c6nc7ccccc7[o]6)ccc55)c4[n]5-c4ccccc4)c3-c3ccccc23)c2ccccc2)cc1 Chemical compound c1ccc(C2(c(cc(cc3)-c(cc4)cc(c5cc(-c6nc7ccccc7[o]6)ccc55)c4[n]5-c4ccccc4)c3-c3ccccc23)c2ccccc2)cc1 XSTDSKHANUJGJF-UHFFFAOYSA-N 0.000 description 1
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- 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
- H05B33/20—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the material in which the electroluminescent material is embedded
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D263/57—Aryl or substituted aryl radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F13/00—Compounds containing elements of Groups 7 or 17 of the Periodic Table
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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
- H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
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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
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- 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
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- H—ELECTRICITY
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- 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
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- 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
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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- 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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- Engineering & Computer Science (AREA)
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- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Manufacturing & Machinery (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JPJP-P-2008-228252 | 2008-09-05 | ||
| JP2008228252 | 2008-09-05 | ||
| JP2009049170A JP5479759B2 (ja) | 2008-09-05 | 2009-03-03 | ベンゾオキサゾール誘導体、発光素子用材料、発光素子、発光装置及び電子機器 |
| JPJP-P-2009-049170 | 2009-03-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100029040A KR20100029040A (ko) | 2010-03-15 |
| KR101670036B1 true KR101670036B1 (ko) | 2016-10-27 |
Family
ID=41798641
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020090082580A Active KR101670036B1 (ko) | 2008-09-05 | 2009-09-02 | 벤조옥사졸 유도체, 벤조옥사졸 유도체를 이용한 발광소자, 발광장치 및 전자기기 |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US8093399B2 (enExample) |
| JP (1) | JP5479759B2 (enExample) |
| KR (1) | KR101670036B1 (enExample) |
| TW (1) | TWI464163B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11980091B2 (en) | 2019-09-30 | 2024-05-07 | Samsung Display Co., Ltd. | Organic electroluminescence device and compound for organic electroluminescence device |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5479759B2 (ja) * | 2008-09-05 | 2014-04-23 | 株式会社半導体エネルギー研究所 | ベンゾオキサゾール誘導体、発光素子用材料、発光素子、発光装置及び電子機器 |
| US8329917B2 (en) | 2009-03-31 | 2012-12-11 | Semiconductor Energy Laboratory Co., Ltd. | Heterocyclic compound and light-emitting element, light-emitting device, lighting device, and electronic device using the same |
| JP5773585B2 (ja) * | 2009-06-29 | 2015-09-02 | 日東電工株式会社 | 発光性トリアリール |
| US20100326526A1 (en) * | 2009-06-29 | 2010-12-30 | Nitto Denko Corporation | Emissive aryl-heteroaryl compounds |
| CN102596939B (zh) * | 2009-09-16 | 2014-08-13 | 日东电工株式会社 | 用于有机发光二极管发射层的化合物 |
| WO2012009283A1 (en) * | 2010-07-13 | 2012-01-19 | Nitto Denko Corporation | Phototherapy methods and devices comprising emissive aryl-heteroaryl compounds |
| US8808879B2 (en) * | 2010-07-19 | 2014-08-19 | Nitto Denko Corporation | Phototherapy devices and methods comprising substituted carbazole compounds |
| EP2428512B1 (en) * | 2010-09-08 | 2014-10-22 | Semiconductor Energy Laboratory Co., Ltd. | Fluorene compound, light-emitting element, light-emitting device, electronic device and lighting device |
| KR20130143034A (ko) | 2010-09-16 | 2013-12-30 | 닛토덴코 가부시키가이샤 | 유기 발광 소자에 사용하기 위한 치환된 비피리딘 |
| JP5872861B2 (ja) * | 2010-11-30 | 2016-03-01 | 株式会社半導体エネルギー研究所 | カルバゾール化合物 |
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Also Published As
| Publication number | Publication date |
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| JP5479759B2 (ja) | 2014-04-23 |
| US20120104376A1 (en) | 2012-05-03 |
| US20100060154A1 (en) | 2010-03-11 |
| TW201016689A (en) | 2010-05-01 |
| KR20100029040A (ko) | 2010-03-15 |
| US8093399B2 (en) | 2012-01-10 |
| TWI464163B (zh) | 2014-12-11 |
| US8735597B2 (en) | 2014-05-27 |
| JP2010083862A (ja) | 2010-04-15 |
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