JP2015144224A5 - - Google Patents

Download PDF

Info

Publication number: JP2015144224A5
Authority: JP; Japan
Prior art keywords: substituted; group; unsubstituted; carbon atoms; ring
Prior art date: 2014-03-14
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.): Granted

Application number

JP2014052133A

Other languages

English (en)

Japanese (ja)

Other versions

JP5905916B2 (ja

JP2015144224A (ja

Filing date

2014-03-14

Publication date

2015-11-05

2014-03-14 Application filed filed Critical

2014-03-14 Priority claimed from JP2014052133A external-priority patent/JP5905916B2/ja

2014-03-14 Priority to JP2014052133A priority Critical patent/JP5905916B2/ja

2014-12-24 Priority to CN201480017162.4A priority patent/CN105103326B/zh

2014-12-24 Priority to KR1020197019230A priority patent/KR20190083000A/ko

2014-12-24 Priority to US14/777,679 priority patent/US9905779B2/en

2014-12-24 Priority to EP14874936.9A priority patent/EP2958158B1/en

2014-12-24 Priority to KR1020187004541A priority patent/KR101997907B1/ko

2014-12-24 Priority to PCT/JP2014/084175 priority patent/WO2015098975A1/ja

2014-12-24 Priority to CN201611221800.1A priority patent/CN106848074B/zh

2014-12-24 Priority to KR1020157025439A priority patent/KR101831211B1/ko

2014-12-24 Priority to EP21152571.2A priority patent/EP3879592B1/en

2015-08-06 Publication of JP2015144224A publication Critical patent/JP2015144224A/ja

2015-11-05 Publication of JP2015144224A5 publication Critical patent/JP2015144224A5/ja

2016-04-20 Publication of JP5905916B2 publication Critical patent/JP5905916B2/ja

2016-04-20 Application granted granted Critical

2018-01-10 Priority to US15/866,616 priority patent/US10811616B2/en

2020-09-01 Priority to US17/009,059 priority patent/US11569456B2/en

2022-12-21 Priority to US18/069,244 priority patent/US20230126981A1/en

Status Active legal-status Critical Current

2034-03-14 Anticipated expiration legal-status Critical

Links

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

JP2014052133A 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 Active JP5905916B2 (ja)

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
CN201611221800.1A CN106848074B (zh)	2013-12-26	2014-12-24	有机电致发光元件及电子设备
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
US14/777,679 US9905779B2 (en)	2013-12-26	2014-12-24	Organic electroluminescent element and electronic device
EP14874936.9A EP2958158B1 (en)	2013-12-26	2014-12-24	Organic electroluminescent element and electronic device
KR1020187004541A KR101997907B1 (ko)	2013-12-26	2014-12-24	유기 일렉트로 루미네센스 소자 및 전자 기기
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
CN201480017162.4A CN105103326B (zh)	2013-12-26	2014-12-24	有机电致发光元件及电子设备
KR1020157025439A KR101831211B1 (ko)	2013-12-26	2014-12-24	유기 일렉트로 루미네센스 소자 및 전자 기기
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 (2)	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 (2)
EP (2)	EP2958158B1 (2)
JP (1)	JP5905916B2 (2)
KR (3)	KR20190083000A (2)
CN (2)	CN105103326B (2)
WO (1)	WO2015098975A1 (2)

Families Citing this family (70)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
KR102543775B1 (ko)	2013-08-14	2023-06-14	가부시키가이샤 큐럭스	유기 일렉트로루미네선스 소자
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
CN110233206B (zh) *	2014-10-07	2021-07-30	出光兴产株式会社	有机电致发光元件、以及电子设备
EP3255693B1 (en)	2015-02-06	2024-10-09	Idemitsu Kosan Co., Ltd	Organic electroluminescence element and electronic device
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
KR102646440B1 (ko) *	2015-07-08	2024-03-13	가부시키가이샤 한도오따이 에네루기 켄큐쇼	발광 소자, 표시 장치, 전자 장치, 및 조명 장치
WO2017025839A1 (en) *	2015-08-07	2017-02-16	Semiconductor Energy Laboratory Co., Ltd.	Light-emitting element, display device, electronic device, and lighting device
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
CN108463894B (zh) *	2015-12-28	2020-03-27	国立大学法人九州大学	有机电致发光元件
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
EP3422431B1 (en) *	2016-02-24	2021-11-03	Idemitsu Kosan Co., Ltd	Organic electroluminescent element and electronic device
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
JP6942127B2 (ja) *	2016-07-08	2021-09-29	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ＭｅｒｃｋＰａｔｅｎｔＧｍｂＨ	有機エレクトロルミネッセンス素子、表示装置、照明装置
JP2019204805A (ja) *	2016-08-10	2019-11-28	出光興産株式会社	有機エレクトロルミネッセンス素子、及び電子機器
JPWO2018088472A1 (ja)	2016-11-09	2019-10-03	出光興産株式会社	化合物、組成物、有機エレクトロルミネッセンス素子、及び電子機器
WO2018097153A1 (ja)	2016-11-25	2018-05-31	コニカミノルタ株式会社	発光性膜、有機エレクトロルミネッセンス素子、有機材料組成物及び有機エレクトロルミネッセンス素子の製造方法
WO2018181188A1 (ja) *	2017-03-31	2018-10-04	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
CN107123749B (zh) *	2017-04-01	2019-08-27	中山大学	一种高显色指数白光有机电致发光器件及其制备方法
KR102389254B1 (ko) *	2017-05-16	2022-04-22	삼성디스플레이 주식회사	헤테로환 화합물 및 이를 포함하는 유기 전계 발광 소자
JP7085176B2 (ja) *	2017-05-30	2022-06-16	株式会社Kyulux	膜、膜の製造方法、有機発光素子、照明装置および化合物
CN108346750B (zh) *	2017-08-08	2019-07-19	广东聚华印刷显示技术有限公司	电致发光器件及其发光层和应用
EP3666851A4 (en) *	2017-08-09	2021-01-13	Okinawa Institute of Science and Technology School Corporation	LIGHT ACCUMULATING COMPOSITION, LIGHT ACCUMULATING ELEMENT AND WAVELENGTH REGULATION METHOD
KR102504132B1 (ko) *	2017-08-21	2023-02-28	삼성디스플레이 주식회사	유기금속 화합물, 이를 포함한 유기 발광 소자 및 상기 유기 발광 소자를 포함한 발광 장치
KR102138430B1 (ko) *	2017-09-06	2020-07-27	주식회사 엘지화학	유기 발광 소자
CN119894227A (zh) *	2017-11-02	2025-04-25	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
KR20250086794A (ko)	2017-12-15	2025-06-13	메르크 파텐트 게엠베하	유기 전계 발광 디바이스용 치환된 방향족 아민
WO2019142555A1 (ja)	2018-01-17	2019-07-25	コニカミノルタ株式会社	発光性膜、有機エレクトロルミネッセンス素子及び有機エレクトロルミネッセンス素子の製造方法
JP2019165102A (ja) *	2018-03-19	2019-09-26	出光興産株式会社	有機エレクトロルミネッセンス素子、及び電子機器
EP3565018B1 (en) *	2018-05-04	2024-05-08	Samsung Display Co., Ltd.	Organic electroluminescent device emitting blue light
JP2021177443A (ja) *	2018-05-28	2021-11-11	出光興産株式会社	有機エレクトロルミネッセンス素子、表示装置及び電子機器
KR20250109799A (ko) *	2018-07-11	2025-07-17	가부시키가이샤 한도오따이 에네루기 켄큐쇼	발광 디바이스, 표시 장치, 전자 기기, 유기 화합물, 및 조명 장치
CN111372918B (zh)	2018-07-27	2023-09-05	出光兴产株式会社	化合物、用于有机电致发光元件的材料、有机电致发光元件以及电子设备
JP7325731B2 (ja) *	2018-08-23	2023-08-15	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
JP2022502829A (ja)	2018-09-24	2022-01-11	メルクパテントゲーエムベーハー	粒状材料を製造するための方法
EP3640999B1 (en) *	2018-10-15	2022-01-05	cynora GmbH	Organic electroluminescent device emitting blue light
KR102717926B1 (ko) *	2018-12-11	2024-10-15	엘지디스플레이 주식회사	유기발광다이오드 및 이를 포함하는 유기발광장치
KR102743332B1 (ko)	2018-12-19	2024-12-18	삼성디스플레이 주식회사	유기 발광 소자 및 이를 포함하는 표시 장치
US20220127286A1 (en)	2019-03-04	2022-04-28	Merck Patent Gmbh	Ligands for nano-sized materials
CN113728074A (zh)	2019-04-25	2021-11-30	株式会社半导体能源研究所	发光器件、发光装置、电子设备及照明装置
JP2022137315A (ja) *	2019-05-27	2022-09-22	出光興産株式会社	有機エレクトロルミネッセンス素子及び電子機器
EP4046210B1 (en) *	2019-10-14	2025-12-17	Samsung Display Co., Ltd.	Organic electroluminescent device emitting light
EP3809479B1 (en) *	2019-10-14	2023-07-12	Samsung Display Co., Ltd.	Organic electroluminescent device emitting blue light
TW202136246A (zh) *	2019-12-19	2021-10-01	德商麥克專利有限公司	電子裝置用化合物
KR102792552B1 (ko)	2020-01-28	2025-04-08	삼성전자주식회사	유기 발광 소자
KR102847111B1 (ko)	2020-04-27	2025-08-18	삼성전자주식회사	유기 발광 소자
US12302748B2 (en)	2020-08-14	2025-05-13	Samsung Display Co., Ltd.	Light-emitting device and electronic apparatus including the same
EP3971261A1 (en)	2020-09-17	2022-03-23	Samsung Electronics Co., Ltd.	Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound
TW202241905A (zh)	2020-12-18	2022-11-01	德商麥克專利有限公司	用於有機電致發光裝置的氮化合物
WO2022129116A1 (de)	2020-12-18	2022-06-23	Merck Patent Gmbh	Indolo[3.2.1-jk]carbazole-6-carbonitril-derivate als blau fluoreszierende emitter zur verwendung in oleds
US20240101560A1 (en)	2020-12-18	2024-03-28	Merck Patent Gmbh	Nitrogenous heteroaromatic compounds for organic electroluminescent devices
KR20220119909A (ko)	2021-02-22	2022-08-30	삼성전자주식회사	헤테로시클릭 화합물, 이를 포함한 유기 발광 소자 및 상기 유기 발광 소자를 포함한 전자 장치
WO2022229234A1 (de)	2021-04-30	2022-11-03	Merck Patent Gmbh	Stickstoffhaltige, heterocyclische verbindungen für organische elektrolumineszenzvorrichtungen
EP4120381A1 (en)	2021-07-16	2023-01-18	Samsung Electronics Co., Ltd.	Organic light-emitting device
KR20230015230A (ko)	2021-07-22	2023-01-31	삼성전자주식회사	유기금속 화합물 및 이를 포함한 유기 발광 소자
KR20240064697A (ko)	2021-09-14	2024-05-13	메르크 파텐트 게엠베하	유기 전계 발광 디바이스용 붕소 복소환 화합물
KR20230041915A (ko)	2021-09-17	2023-03-27	삼성전자주식회사	유기 발광 소자
EP4423209B1 (de)	2021-10-27	2025-05-07	Merck Patent GmbH	Bor- und stickstoffhaltige, heterocyclische verbindungen für organische elektrolumineszenzvorrichtungen
JP7780178B2 (ja) *	2021-11-08	2025-12-04	株式会社Kyulux	化合物、組成物、ホスト材料および有機発光素子
EP4199130A1 (en)	2021-12-15	2023-06-21	Idemitsu Kosan Co.,Ltd.	An organic electroluminescence device comprising a light emitting layer comprising three different compounds and an electronic equipment comprising said organic electroluminescence device
WO2023161167A1 (de)	2022-02-23	2023-08-31	Merck Patent Gmbh	Stickstoffhaltige heterocyclen für organische elektrolumineszenzvorrichtungen
WO2023161168A1 (de)	2022-02-23	2023-08-31	Merck Patent Gmbh	Aromatische heterocyclen für organische elektrolumineszenzvorrichtungen
KR20240019643A (ko)	2022-08-04	2024-02-14	삼성전자주식회사	디스플레이 장치
KR20240019644A (ko)	2022-08-04	2024-02-14	삼성전자주식회사	디스플레이 장치
KR20250151490A (ko)	2023-02-17	2025-10-21	메르크 파텐트 게엠베하	유기 전계발광 디바이스용 재료
CN121487940A (zh)	2023-07-12	2026-02-06	默克专利有限公司	用于电子器件的材料
WO2025196145A1 (en)	2024-03-22	2025-09-25	Merck Patent Gmbh	Materials for organic light emitting devices

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP3825725B2 (ja)	1998-05-19	2006-09-27	三洋電機株式会社	有機エレクトロルミネッセンス素子
JP2002184581A (ja) *	2000-12-13	2002-06-28	Sanyo Electric Co Ltd	有機発光素子
TW556446B (en) *	2002-09-11	2003-10-01	Opto Tech Corp	Organic light-emitting device and the manufacturing method thereof
JP4789475B2 (ja)	2004-03-10	2011-10-12	富士フイルム株式会社	発光素子
JP4629715B2 (ja) *	2006-12-06	2011-02-09	韓國電子通信研究院	Ｏｌｅｄ素子
US20080284318A1 (en) *	2007-05-17	2008-11-20	Deaton Joseph C	Hybrid fluorescent/phosphorescent oleds
US8080658B2 (en)	2007-07-10	2011-12-20	Idemitsu Kosan Co., Ltd.	Material for organic electroluminescent element and organic electroluminescent element employing the same
JP5213405B2 (ja) *	2007-10-04	2013-06-19	出光興産株式会社	有機エレクトロルミネッセンス素子
JP5124785B2 (ja) *	2009-12-07	2013-01-23	新日鉄住金化学株式会社	有機発光材料及び有機発光素子
US8456081B2 (en)	2010-06-03	2013-06-04	The University Of Southern California	Ultrabright fluorescent OLEDS using triplet sinks
WO2012008331A1 (ja) *	2010-07-12	2012-01-19	出光興産株式会社	有機エレクトロルミネッセンス素子
TWI552406B (zh)	2011-03-25	2016-10-01	出光興產股份有限公司	有機電致發光元件
JPWO2012153780A1 (ja)	2011-05-11	2014-07-31	出光興産株式会社	新規化合物、有機エレクトロルミネッセンス素子用材料及び有機エレクトロルミネッセンス素子
US9978952B2 (en)	2011-09-13	2018-05-22	Idemitsu Kosan Co., Ltd.	Fused heterocyclic aromatic derivative, organic electroluminescence element material, and organic electroluminescence element using same
CN102709485B (zh)	2011-09-30	2016-05-25	昆山维信诺显示技术有限公司	一种有机电致发光器件及其制备方法
JP2013116975A (ja)	2011-12-02	2013-06-13	Kyushu Univ	遅延蛍光材料、有機発光素子および化合物
JP2013168587A (ja) *	2012-02-16	2013-08-29	Sharp Corp	発光装置、半導体レーザ素子、および照明装置
JP2014135466A (ja)	2012-04-09	2014-07-24	Kyushu Univ	有機発光素子ならびにそれに用いる発光材料および化合物
JP6158542B2 (ja)	2012-04-13	2017-07-05	株式会社半導体エネルギー研究所	発光素子、発光装置、電子機器、および照明装置
JP6158543B2 (ja) *	2012-04-13	2017-07-05	株式会社半導体エネルギー研究所	発光素子、発光装置、電子機器、および照明装置
JP6076153B2 (ja) *	2012-04-20	2017-02-08	株式会社半導体エネルギー研究所	発光素子、発光装置、表示装置、電子機器及び照明装置
US8994013B2 (en) *	2012-05-18	2015-03-31	Semiconductor Energy Laboratory Co., Ltd.	Light-emitting element, light-emitting device, display device, electronic device, and lighting device
WO2013180241A1 (ja)	2012-06-01	2013-12-05	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有機エレクトロルミネッセンス素子用材料
TWI666299B (zh) *	2012-08-03	2019-07-21	日商半導體能源研究所股份有限公司	發光元件
US10957870B2 (en)	2012-09-07	2021-03-23	Universal Display Corporation	Organic light emitting device
US9209411B2 (en) *	2012-12-07	2015-12-08	Universal Display Corporation	Organic electroluminescent materials and devices
TWI661589B (zh) *	2013-03-29	2019-06-01	日商九州有機光材股份有限公司	有機電致發光元件
CN203242670U (zh) *	2013-04-27	2013-10-16	四川虹视显示技术有限公司	一种顶发光oled器件的薄膜封装结构
GB2514818B (en) *	2013-06-05	2015-12-16	Cambridge Display Tech Ltd	Polymer and organic electronic device
KR102543775B1 (ko) *	2013-08-14	2023-06-14	가부시키가이샤 큐럭스	유기 일렉트로루미네선스 소자
EP3916822B1 (en)	2013-12-20	2025-08-06	UDC Ireland Limited	Highly efficient oled devices with very short decay times

2014
- 2014-03-14 JP JP2014052133A patent/JP5905916B2/ja active Active
- 2014-12-24 KR KR1020197019230A patent/KR20190083000A/ko not_active Ceased
- 2014-12-24 KR KR1020157025439A patent/KR101831211B1/ko active Active
- 2014-12-24 CN CN201480017162.4A patent/CN105103326B/zh active Active
- 2014-12-24 EP EP14874936.9A patent/EP2958158B1/en active Active
- 2014-12-24 CN CN201611221800.1A patent/CN106848074B/zh active Active
- 2014-12-24 KR KR1020187004541A patent/KR101997907B1/ko active Active
- 2014-12-24 EP EP21152571.2A patent/EP3879592B1/en active Active
- 2014-12-24 WO PCT/JP2014/084175 patent/WO2015098975A1/ja not_active Ceased
- 2014-12-24 US US14/777,679 patent/US9905779B2/en active Active
2018
- 2018-01-10 US US15/866,616 patent/US10811616B2/en active Active
2020
- 2020-09-01 US US17/009,059 patent/US11569456B2/en active Active
2022
- 2022-12-21 US US18/069,244 patent/US20230126981A1/en active Pending

Publication	Publication Date	Title
JP2015144224A5 (2)	2015-11-05
JP5905916B2 (ja)	2016-04-20	有機エレクトロルミネッセンス素子および電子機器
JP6668152B2 (ja)	2020-03-18	化合物、発光材料および有機発光素子
JP6482782B2 (ja)	2019-03-13	有機発光素子
JP6326251B2 (ja)	2018-05-16	発光材料及びそれを用いた有機ｅｌ素子
TWI633170B (zh)	2018-08-21	有機電致發光元件
JP6293417B2 (ja)	2018-03-14	化合物、発光材料および有機発光素子
JP6383538B2 (ja)	2018-08-29	発光材料、有機発光素子および化合物
KR102660767B1 (ko)	2024-04-24	유기 일렉트로루미네센스 소자 및 전자 기기
JPWO2015072470A1 (ja)	2017-03-16	発光材料、並びに、これを用いた遅延蛍光体および有機発光素子
JPWO2013161437A1 (ja)	2015-12-24	発光材料および有機発光素子
TW201531552A (zh)	2015-08-16	發光材料、有機發光元件及化合物
JP2014009224A (ja)	2014-01-20	発光材料、化合物および有機発光素子
JP6647514B2 (ja)	2020-02-14	有機発光素子ならびにそれに用いる発光材料および化合物
WO2018030446A1 (ja)	2018-02-15	有機エレクトロルミネッセンス素子、及び電子機器
JP2020515053A (ja)	2020-05-21	有機エレクトロルミネセントデバイス
WO2017146191A1 (ja)	2017-08-31	有機エレクトロルミネッセンス素子、及び電子機器
KR20140073695A (ko)	2014-06-17	유기 전계 발광 화합물 및 이를 포함하는 유기 전계 발광 소자
JP2025150737A (ja)	2025-10-09	化合物、有機エレクトロルミネッセンス素子及び電子機器
JP2015106659A (ja)	2015-06-08	有機エレクトロルミネッセンス素子および電子機器
Chen et al.	2022	Benzimidazole-substituted bisanthracene: a highly efficient deep-blue triplet–triplet fusion OLED emitter at low dopant concentration
JP2018127424A (ja)	2018-08-16	新規イミダゾール誘導体、及びそれを用いた有機ｅｌ素子
JP2019006988A (ja)	2019-01-17	発光材料、化合物、遅延蛍光体および発光素子
JP7547072B2 (ja)	2024-09-09	化合物、有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子及び電子機器
JP2018035135A (ja)	2018-03-08	新規イソニコチノニトリル誘導体、及びそれを用いた有機ｅｌ素子