JP2015144224A5 - - Google Patents
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- JP2015144224A5 JP2015144224A5 JP2014052133A JP2014052133A JP2015144224A5 JP 2015144224 A5 JP2015144224 A5 JP 2015144224A5 JP 2014052133 A JP2014052133 A JP 2014052133A JP 2014052133 A JP2014052133 A JP 2014052133A JP 2015144224 A5 JP2015144224 A5 JP 2015144224A5
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- JP
- Japan
- Prior art keywords
- substituted
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- carbon atoms
- ring
- Prior art date
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 135
- 239000000463 material Substances 0.000 claims description 95
- 125000001424 substituent group Chemical group 0.000 claims description 67
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 45
- 238000005401 electroluminescence Methods 0.000 claims description 36
- -1 CR 32 Chemical group 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 29
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 27
- 229910052717 sulfur Inorganic materials 0.000 claims description 25
- 125000004434 sulfur atom Chemical group 0.000 claims description 25
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 23
- 150000001875 compounds Chemical class 0.000 claims description 21
- 229910052757 nitrogen Inorganic materials 0.000 claims description 21
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 21
- 125000006413 ring segment Chemical group 0.000 claims description 21
- 125000000623 heterocyclic group Chemical group 0.000 claims description 20
- 125000004429 atom Chemical group 0.000 claims description 18
- 230000003111 delayed effect Effects 0.000 claims description 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 17
- 229910052799 carbon Inorganic materials 0.000 claims description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 125000005843 halogen group Chemical group 0.000 claims description 11
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 9
- 125000005106 triarylsilyl group Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 125000005103 alkyl silyl group Chemical group 0.000 claims description 7
- 125000004414 alkyl thio group Chemical group 0.000 claims description 7
- 125000005104 aryl silyl group Chemical group 0.000 claims description 7
- 125000005110 aryl thio group Chemical group 0.000 claims description 7
- 125000004104 aryloxy group Chemical group 0.000 claims description 7
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 5
- 238000004020 luminiscence type Methods 0.000 claims description 2
- 230000001747 exhibiting effect Effects 0.000 claims 2
- UWRZIZXBOLBCON-VOTSOKGWSA-N (e)-2-phenylethenamine Chemical class N\C=C\C1=CC=CC=C1 UWRZIZXBOLBCON-VOTSOKGWSA-N 0.000 claims 1
- YZVWKHVRBDQPMQ-UHFFFAOYSA-N 1-aminopyrene Chemical class C1=C2C(N)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 YZVWKHVRBDQPMQ-UHFFFAOYSA-N 0.000 claims 1
- YUENFNPLGJCNRB-UHFFFAOYSA-N anthracen-1-amine Chemical class C1=CC=C2C=C3C(N)=CC=CC3=CC2=C1 YUENFNPLGJCNRB-UHFFFAOYSA-N 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 1
- OQENBJBTQPIZKA-UHFFFAOYSA-N chrysen-1-amine Chemical class C1=CC2=C3C=CC=CC3=CC=C2C2=C1C(N)=CC=C2 OQENBJBTQPIZKA-UHFFFAOYSA-N 0.000 claims 1
- 150000004696 coordination complex Chemical class 0.000 claims 1
- 230000008878 coupling Effects 0.000 claims 1
- 238000010168 coupling process Methods 0.000 claims 1
- 238000005859 coupling reaction Methods 0.000 claims 1
- 150000004985 diamines Chemical class 0.000 claims 1
- 150000002219 fluoranthenes Chemical class 0.000 claims 1
- 150000002220 fluorenes Chemical class 0.000 claims 1
- 150000003220 pyrenes Chemical class 0.000 claims 1
- 125000005259 triarylamine group Chemical group 0.000 claims 1
- 238000001296 phosphorescence spectrum Methods 0.000 description 14
- 238000005259 measurement Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 239000010453 quartz Substances 0.000 description 7
- 230000000630 rising effect Effects 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 125000003342 alkenyl group Chemical group 0.000 description 6
- 125000000304 alkynyl group Chemical group 0.000 description 6
- 101100152731 Arabidopsis thaliana TH2 gene Proteins 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 238000001228 spectrum Methods 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 2
- 125000002676 chrysenyl group Chemical group C1(=CC=CC=2C3=CC=C4C=CC=CC4=C3C=CC12)* 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
- 239000002019 doping agent Substances 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 239000007850 fluorescent dye Substances 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 230000001052 transient effect Effects 0.000 description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N 1H-imidazole Chemical compound C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004663 dialkyl amino group Chemical group 0.000 description 1
- 125000004986 diarylamino group Chemical group 0.000 description 1
- 125000005299 dibenzofluorenyl group Chemical group C1(=CC=CC2=C3C(=C4C=5C=CC=CC5CC4=C21)C=CC=C3)* 0.000 description 1
- 125000005509 dibenzothiophenyl group Chemical group 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 125000003914 fluoranthenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC=C4C1=C23)* 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 125000003838 furazanyl group Chemical group 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 125000001977 isobenzofuranyl group Chemical group C=1(OC=C2C=CC=CC12)* 0.000 description 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
- 125000005956 isoquinolyl group Chemical group 0.000 description 1
- MJIHNNLFOKEZEW-UHFFFAOYSA-N lansoprazole Chemical compound CC1=C(OCC(F)(F)F)C=CN=C1CS(=O)C1=NC2=CC=CC=C2N1 MJIHNNLFOKEZEW-UHFFFAOYSA-N 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 125000004934 phenanthridinyl group Chemical group C1(=CC=CC2=NC=C3C=CC=CC3=C12)* 0.000 description 1
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001644 phenoxazinyl group Chemical group C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000005017 substituted alkenyl group Chemical group 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2014052133A JP5905916B2 (ja) | 2013-12-26 | 2014-03-14 | 有機エレクトロルミネッセンス素子および電子機器 |
| KR1020187004541A KR101997907B1 (ko) | 2013-12-26 | 2014-12-24 | 유기 일렉트로 루미네센스 소자 및 전자 기기 |
| EP14874936.9A EP2958158B1 (en) | 2013-12-26 | 2014-12-24 | Organic electroluminescent element and electronic device |
| CN201480017162.4A CN105103326B (zh) | 2013-12-26 | 2014-12-24 | 有机电致发光元件及电子设备 |
| PCT/JP2014/084175 WO2015098975A1 (ja) | 2013-12-26 | 2014-12-24 | 有機エレクトロルミネッセンス素子および電子機器 |
| EP21152571.2A EP3879592B1 (en) | 2013-12-26 | 2014-12-24 | Organic electroluminescent element and electronic device |
| KR1020197019230A KR20190083000A (ko) | 2013-12-26 | 2014-12-24 | 유기 일렉트로 루미네센스 소자 및 전자 기기 |
| KR1020157025439A KR101831211B1 (ko) | 2013-12-26 | 2014-12-24 | 유기 일렉트로 루미네센스 소자 및 전자 기기 |
| CN201611221800.1A CN106848074B (zh) | 2013-12-26 | 2014-12-24 | 有机电致发光元件及电子设备 |
| US14/777,679 US9905779B2 (en) | 2013-12-26 | 2014-12-24 | Organic electroluminescent element and electronic device |
| US15/866,616 US10811616B2 (en) | 2013-12-26 | 2018-01-10 | Organic electroluminescent element and electronic device |
| US17/009,059 US11569456B2 (en) | 2013-12-26 | 2020-09-01 | Organic electroluminescent element and electronic device |
| US18/069,244 US20230126981A1 (en) | 2013-12-26 | 2022-12-21 | Organic electroluminescent element and electronic device |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013270267 | 2013-12-26 | ||
| JP2013270267 | 2013-12-26 | ||
| JP2014052133A JP5905916B2 (ja) | 2013-12-26 | 2014-03-14 | 有機エレクトロルミネッセンス素子および電子機器 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016054319A Division JP6433935B2 (ja) | 2013-12-26 | 2016-03-17 | 有機エレクトロルミネッセンス素子および電子機器 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015144224A JP2015144224A (ja) | 2015-08-06 |
| JP2015144224A5 true JP2015144224A5 (https=) | 2015-11-05 |
| JP5905916B2 JP5905916B2 (ja) | 2016-04-20 |
Family
ID=53478824
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014052133A Active JP5905916B2 (ja) | 2013-12-26 | 2014-03-14 | 有機エレクトロルミネッセンス素子および電子機器 |
Country Status (6)
| Country | Link |
|---|---|
| US (4) | US9905779B2 (https=) |
| EP (2) | EP3879592B1 (https=) |
| JP (1) | JP5905916B2 (https=) |
| KR (3) | KR101997907B1 (https=) |
| CN (2) | CN106848074B (https=) |
| WO (1) | WO2015098975A1 (https=) |
Families Citing this family (70)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10862047B2 (en) | 2013-08-14 | 2020-12-08 | Kyushu University, National University Corporation | Organic electroluminescent device |
| JP6374329B2 (ja) * | 2014-06-26 | 2018-08-15 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子、有機エレクトロルミネッセンス素子用材料、および電子機器 |
| JP6482782B2 (ja) * | 2014-07-18 | 2019-03-13 | 国立大学法人九州大学 | 有機発光素子 |
| EP3188271B1 (en) * | 2014-08-26 | 2022-05-04 | Idemitsu Kosan Co., Ltd | Organic electroluminescent element and electronic device |
| JP2017212024A (ja) * | 2014-08-28 | 2017-11-30 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子および電子機器 |
| JP6722579B2 (ja) * | 2014-10-07 | 2020-07-15 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子、および電子機器 |
| KR102660767B1 (ko) | 2015-02-06 | 2024-04-24 | 이데미쓰 고산 가부시키가이샤 | 유기 일렉트로루미네센스 소자 및 전자 기기 |
| DE102015106941B4 (de) * | 2015-05-05 | 2025-07-31 | Pictiva Displays International Limited | Organische Emitterschicht, organische Leuchtdiode und Verwendung von Schweratomen in einer organischen Emitterschicht einer organischen Leuchtdiode |
| KR20250105465A (ko) * | 2015-07-08 | 2025-07-08 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 표시 장치, 전자 장치, 및 조명 장치 |
| CN111710788B (zh) * | 2015-08-07 | 2023-07-21 | 株式会社半导体能源研究所 | 发光元件、显示装置、电子设备及照明装置 |
| KR20170034067A (ko) * | 2015-09-18 | 2017-03-28 | 엘지디스플레이 주식회사 | 유기 발광 표시 장치 |
| WO2017065295A1 (ja) * | 2015-10-15 | 2017-04-20 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子および電子機器 |
| JP6739804B2 (ja) * | 2015-12-28 | 2020-08-12 | 国立大学法人九州大学 | 有機エレクトロルミネッセンス素子 |
| JP6668152B2 (ja) * | 2015-12-28 | 2020-03-18 | 株式会社Ｋｙｕｌｕｘ | 化合物、発光材料および有機発光素子 |
| KR102739330B1 (ko) * | 2016-02-24 | 2024-12-05 | 이데미쓰 고산 가부시키가이샤 | 유기 일렉트로루미네센스 소자 및 전자 기기 |
| JP7253646B2 (ja) * | 2016-04-28 | 2023-04-06 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | π共役系化合物、有機エレクトロルミネッセンス素子材料、発光材料、電荷輸送材料、発光性薄膜、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 |
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- 2014-12-24 KR KR1020197019230A patent/KR20190083000A/ko not_active Ceased
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