KR20170067424A - 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 - Google Patents
유기 화합물 및 이를 포함하는 유기 전계 발광 소자 Download PDFInfo
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- KR20170067424A KR20170067424A KR1020150174084A KR20150174084A KR20170067424A KR 20170067424 A KR20170067424 A KR 20170067424A KR 1020150174084 A KR1020150174084 A KR 1020150174084A KR 20150174084 A KR20150174084 A KR 20150174084A KR 20170067424 A KR20170067424 A KR 20170067424A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- aryl
- compound
- phenyl
- alkyl
- Prior art date
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- 150000002894 organic compounds Chemical class 0.000 title claims description 7
- 238000005401 electroluminescence Methods 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 172
- 239000010410 layer Substances 0.000 claims description 87
- -1 alkyl boron Chemical compound 0.000 claims description 80
- 125000003118 aryl group Chemical group 0.000 claims description 70
- 125000004429 atom Chemical group 0.000 claims description 37
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- 239000000126 substance Substances 0.000 claims description 30
- 125000003342 alkenyl group Chemical group 0.000 claims description 27
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 27
- 125000003545 alkoxy group Chemical group 0.000 claims description 26
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 25
- 125000004104 aryloxy group Chemical group 0.000 claims description 24
- 125000005103 alkyl silyl group Chemical group 0.000 claims description 23
- 125000000304 alkynyl group Chemical group 0.000 claims description 22
- 125000001424 substituent group Chemical group 0.000 claims description 22
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 21
- 125000005104 aryl silyl group Chemical group 0.000 claims description 18
- 125000005264 aryl amine group Chemical group 0.000 claims description 16
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 15
- 239000008280 blood Substances 0.000 claims description 14
- 210000004369 blood Anatomy 0.000 claims description 14
- 239000012044 organic layer Substances 0.000 claims description 14
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 12
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 11
- 150000002367 halogens Chemical class 0.000 claims description 11
- 229910052796 boron Inorganic materials 0.000 claims description 9
- 229910052805 deuterium Inorganic materials 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 150000004982 aromatic amines Chemical class 0.000 claims description 4
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 125000005549 heteroarylene group Chemical group 0.000 claims description 3
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims description 2
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- YCWSUKQGVSGXJO-NTUHNPAUSA-N nifuroxazide Chemical group C1=CC(O)=CC=C1C(=O)N\N=C\C1=CC=C([N+]([O-])=O)O1 YCWSUKQGVSGXJO-NTUHNPAUSA-N 0.000 claims 1
- 239000011368 organic material Substances 0.000 abstract description 10
- 230000015572 biosynthetic process Effects 0.000 description 49
- 238000003786 synthesis reaction Methods 0.000 description 49
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 43
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 38
- 239000000463 material Substances 0.000 description 31
- 230000000052 comparative effect Effects 0.000 description 11
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- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 239000004305 biphenyl Substances 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 125000000319 biphenyl-4-yl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 description 8
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 7
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 7
- 239000002019 doping agent Substances 0.000 description 7
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- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
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- ZDZHCHYQNPQSGG-UHFFFAOYSA-N 1-naphthalen-1-ylnaphthalene Chemical group C1=CC=C2C(C=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 description 5
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- 239000002184 metal Substances 0.000 description 4
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- IXOCHQYWUPOZKG-UHFFFAOYSA-N 2-(2-bromophenyl)-1,3,5-triazine Chemical compound BrC1=CC=CC=C1C1=NC=NC=N1 IXOCHQYWUPOZKG-UHFFFAOYSA-N 0.000 description 3
- NTEIZPBYXABJKN-UHFFFAOYSA-N 2-(4-chlorophenyl)-4,6-diphenyl-1,3,5-triazine Chemical compound C1=CC(Cl)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 NTEIZPBYXABJKN-UHFFFAOYSA-N 0.000 description 3
- IJUDEFZBMMRSNM-UHFFFAOYSA-N 2-bromo-1-(2-bromonaphthalen-1-yl)naphthalene Chemical compound C1=CC=C2C(C3=C4C=CC=CC4=CC=C3Br)=C(Br)C=CC2=C1 IJUDEFZBMMRSNM-UHFFFAOYSA-N 0.000 description 3
- DDGPPAMADXTGTN-UHFFFAOYSA-N 2-chloro-4,6-diphenyl-1,3,5-triazine Chemical compound N=1C(Cl)=NC(C=2C=CC=CC=2)=NC=1C1=CC=CC=C1 DDGPPAMADXTGTN-UHFFFAOYSA-N 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
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- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 2
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- 238000000746 purification Methods 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
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- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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- CAYQIZIAYYNFCS-UHFFFAOYSA-N (4-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=C(Cl)C=C1 CAYQIZIAYYNFCS-UHFFFAOYSA-N 0.000 description 1
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- PVGOPEUJUVXCGN-UHFFFAOYSA-N 2,4-diphenyl-6-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,5-triazine Chemical compound O1C(C)(C)C(C)(C)OB1C1=CC=C(C=2N=C(N=C(N=2)C=2C=CC=CC=2)C=2C=CC=CC=2)C=C1 PVGOPEUJUVXCGN-UHFFFAOYSA-N 0.000 description 1
- UYYNISZZEVRNCF-UHFFFAOYSA-N 2-(4-bromophenyl)-1,3,5-triazine Chemical compound C1=CC(Br)=CC=C1C1=NC=NC=N1 UYYNISZZEVRNCF-UHFFFAOYSA-N 0.000 description 1
- ZMRZEUVCCWAUIG-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-phenyl-6-(4-phenylphenyl)-1,3,5-triazine Chemical compound C1=CC(Cl)=CC=C1C1=NC(C2=CC=C(C3=CC=CC=C3)C=C2)=NC(=N1)C1=CC=CC=C1 ZMRZEUVCCWAUIG-UHFFFAOYSA-N 0.000 description 1
- IHTLUVKZKPLZFY-UHFFFAOYSA-N 2-[4-[1-(2-bromonaphthalen-1-yl)naphthalen-2-yl]phenyl]-4,6-diphenyl-1,3,5-triazine Chemical compound BrC1=C(C2=CC=CC=C2C=C1)C1=C(C=CC2=CC=CC=C12)C1=CC=C(C=C1)C1=NC(=NC(=N1)C1=CC=CC=C1)C1=CC=CC=C1 IHTLUVKZKPLZFY-UHFFFAOYSA-N 0.000 description 1
- SWMZZVHPRNATOQ-UHFFFAOYSA-N 2-[4-[4-(4-bromonaphthalen-1-yl)naphthalen-1-yl]phenyl]-4,6-diphenyl-1,3,5-triazine Chemical compound BrC1=CC=C(C2=CC=CC=C12)C1=CC=C(C2=CC=CC=C12)C1=CC=C(C=C1)C1=NC(=NC(=N1)C1=CC=CC=C1)C1=CC=CC=C1 SWMZZVHPRNATOQ-UHFFFAOYSA-N 0.000 description 1
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- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
- C07C15/20—Polycyclic condensed hydrocarbons
- C07C15/24—Polycyclic condensed hydrocarbons containing two rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/26—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/24—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to three ring carbon atoms
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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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- H01L51/0052—
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- H01L51/0067—
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- H01L51/50—
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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
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/14—Carrier transporting layers
- H10K50/16—Electron transporting layers
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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
- H10K85/30—Coordination compounds
- H10K85/361—Polynuclear complexes, i.e. complexes comprising two or more metal centers
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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
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
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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
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
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- C—CHEMISTRY; METALLURGY
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1059—Heterocyclic compounds characterised by ligands containing three nitrogen atoms as heteroatoms
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- 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
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Optics & Photonics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- High Energy & Nuclear Physics (AREA)
- Inorganic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
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| KR1020150174084A KR20170067424A (ko) | 2015-12-08 | 2015-12-08 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| PCT/KR2016/014112 WO2017099430A1 (fr) | 2015-12-08 | 2016-12-02 | Composé organique et dispositif électroluminescent organique le comprenant |
| KR1020230095925A KR20230117301A (ko) | 2015-12-08 | 2023-07-24 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| KR1020150174084A KR20170067424A (ko) | 2015-12-08 | 2015-12-08 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
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| KR1020230095925A Division KR20230117301A (ko) | 2015-12-08 | 2023-07-24 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
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| KR1020230095925A KR20230117301A (ko) | 2015-12-08 | 2023-07-24 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
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| KR1020230095925A KR20230117301A (ko) | 2015-12-08 | 2023-07-24 | 유기 화합물 및 이를 포함하는 유기 전계 발광 소자 |
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| Country | Link |
|---|---|
| KR (2) | KR20170067424A (fr) |
| WO (1) | WO2017099430A1 (fr) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110248928A (zh) * | 2017-05-31 | 2019-09-17 | 株式会社Lg化学 | 新型杂环化合物及利用其的有机发光元件 |
| KR20200072125A (ko) * | 2018-12-12 | 2020-06-22 | 엘지디스플레이 주식회사 | 유기 화합물, 이를 포함하는 발광다이오드 및 발광장치 |
| WO2020180005A1 (fr) * | 2019-03-05 | 2020-09-10 | 주식회사 엘지화학 | Composé binaphtalène et dispositif électroluminescent organique le comprenant |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2018221985A1 (fr) * | 2017-05-31 | 2018-12-06 | 주식회사 엘지화학 | Nouveau composé hétérocyclique et élément électroluminescent organique l'utilisant |
| KR102064993B1 (ko) | 2017-05-31 | 2020-01-10 | 주식회사 엘지화학 | 신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 |
| WO2018221986A1 (fr) * | 2017-05-31 | 2018-12-06 | 주식회사 엘지화학 | Nouveau composé hétérocyclique et élément électroluminescent organique l'utilisant |
| CN117466824A (zh) * | 2018-03-22 | 2024-01-30 | 株式会社Lg化学 | 化合物和包含其的有机发光器件 |
| CN108623430A (zh) * | 2018-07-19 | 2018-10-09 | 石家庄诚志永华显示材料有限公司 | 联萘衍生物、包含该联萘衍生物的材料和有机电致发光器件 |
| KR102625755B1 (ko) * | 2018-12-03 | 2024-01-15 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기 발광 소자 |
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| JP2009246097A (ja) * | 2008-03-31 | 2009-10-22 | Konica Minolta Holdings Inc | 有機エレクトロルミネッセンス素子、表示装置、及び照明装置 |
| KR101512012B1 (ko) * | 2013-02-14 | 2015-04-16 | (주)씨에스엘쏠라 | 유기 발광 화합물 및 이를 이용한 유기 발광 소자 |
| WO2014163173A1 (fr) * | 2013-04-04 | 2014-10-09 | Jnc株式会社 | Matériau de transport d'électrons et dispositif électroluminescent organique l'utilisant |
| TWI632140B (zh) * | 2013-08-07 | 2018-08-11 | 捷恩智股份有限公司 | 用於電子輸送材料的化合物、電子輸送材料及使用其的有機電激發光元件 |
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2015
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2023
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110248928A (zh) * | 2017-05-31 | 2019-09-17 | 株式会社Lg化学 | 新型杂环化合物及利用其的有机发光元件 |
| CN110248928B (zh) * | 2017-05-31 | 2022-07-08 | 株式会社Lg化学 | 新型杂环化合物及利用其的有机发光元件 |
| KR20200072125A (ko) * | 2018-12-12 | 2020-06-22 | 엘지디스플레이 주식회사 | 유기 화합물, 이를 포함하는 발광다이오드 및 발광장치 |
| WO2020180005A1 (fr) * | 2019-03-05 | 2020-09-10 | 주식회사 엘지화학 | Composé binaphtalène et dispositif électroluminescent organique le comprenant |
| KR20200106821A (ko) * | 2019-03-05 | 2020-09-15 | 주식회사 엘지화학 | 바이나프탈렌 화합물 및 이를 포함하는 유기 발광 소자 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2017099430A1 (fr) | 2017-06-15 |
| KR20230117301A (ko) | 2023-08-08 |
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