CA3016789A1 - Molecules organiques, destinees en particulier aux dispositifs optoelectroniques - Google Patents

Molecules organiques, destinees en particulier aux dispositifs optoelectroniques Download PDF

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Publication number: CA3016789A1
Authority: CA; Canada
Prior art keywords: group; optionally substituted; organic; independently; substituents
Prior art date: 2017-09-12
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.): Pending

Application number

CA3016789A

Other languages

English (en)

Inventor

Sebastian Duck

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Samsung Display Co Ltd

Original Assignee

Cynora GmbH

Priority date (The priority date 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 date listed.)

2017-09-12

Filing date

2018-09-07

Publication date

2019-03-12

2018-09-07 Application filed by Cynora GmbH filed Critical Cynora GmbH

2019-03-12 Publication of CA3016789A1 publication Critical patent/CA3016789A1/fr

Status Pending legal-status Critical Current

Links

230000005693 optoelectronics Effects 0.000 title claims abstract description 21
125000001424 substituent group Chemical group 0.000 claims abstract description 53
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229910052805 deuterium Inorganic materials 0.000 claims abstract description 26
150000002431 hydrogen Chemical class 0.000 claims abstract description 16
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 16
239000001257 hydrogen Substances 0.000 claims abstract description 16
150000002894 organic compounds Chemical class 0.000 claims abstract 3
125000006749 (C6-C60) aryl group Chemical group 0.000 claims abstract 2
239000000463 material Substances 0.000 claims description 24
239000002904 solvent Substances 0.000 claims description 14
125000003118 aryl group Chemical group 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 13
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238000006243 chemical reaction Methods 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
125000004122 cyclic group Chemical group 0.000 claims description 4
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SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
125000002255 pentenyl group Chemical group C(=CCCC)* 0.000 description 1
125000005981 pentynyl group Chemical group 0.000 description 1
125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
239000012071 phase Substances 0.000 description 1
229950000688 phenothiazine Drugs 0.000 description 1
150000003004 phosphinoxides Chemical class 0.000 description 1
238000001296 phosphorescence spectrum Methods 0.000 description 1
238000000628 photoluminescence spectroscopy Methods 0.000 description 1
238000005240 physical vapour deposition Methods 0.000 description 1
239000002985 plastic film Substances 0.000 description 1
229920006255 plastic film Polymers 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920000767 polyaniline Polymers 0.000 description 1
229920000123 polythiophene Polymers 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 description 1
PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 1
238000000275 quality assurance Methods 0.000 description 1
JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
230000002040 relaxant effect Effects 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000010561 standard procedure Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000003115 supporting electrolyte Substances 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
125000005309 thioalkoxy group Chemical group 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
230000036962 time dependent Effects 0.000 description 1
229910001887 tin oxide Inorganic materials 0.000 description 1
QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(II) oxide Inorganic materials [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
229910052723 transition metal Chemical class 0.000 description 1
229910000314 transition metal oxide Inorganic materials 0.000 description 1
150000003624 transition metals Chemical class 0.000 description 1
238000002834 transmittance Methods 0.000 description 1
125000005259 triarylamine group Chemical group 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
SLGBZMMZGDRARJ-UHFFFAOYSA-N triphenylene Chemical compound C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
238000007740 vapor deposition Methods 0.000 description 1
238000005019 vapor deposition process Methods 0.000 description 1
238000001947 vapour-phase growth Methods 0.000 description 1
239000003643 water by type Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1
YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
229910001928 zirconium oxide Inorganic materials 0.000 description 1

Classifications

- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells

Landscapes

Electroluminescent Light Sources (AREA)

CA3016789A 2017-09-12 2018-09-07 Molecules organiques, destinees en particulier aux dispositifs optoelectroniques Pending CA3016789A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE102017121106		2017-09-12
DE102017121106.3		2017-09-12

Publications (1)

Publication Number	Publication Date
CA3016789A1 true CA3016789A1 (fr)	2019-03-12

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Application Number	Title	Priority Date	Filing Date
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Country Status (1)

Country	Link
CA (1)	CA3016789A1 (fr)

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CN111333671A (zh) *	2020-03-16	2020-06-26	清华大学	一种发光材料及其应用以及包含其的有机电致发光器件
WO2020217229A1 (fr)	2019-04-26	2020-10-29	Idemitsu Kosan Co., Ltd.	Composé polycyclique et dispositif électroluminescent organique comprenant le composé polycyclique ou une composition
WO2021020929A1 (fr) *	2019-08-01	2021-02-04	주식회사 엘지화학	Composé et dispositif électroluminescent organique le comprenant
WO2021122757A1 (fr) *	2019-12-20	2021-06-24	Cynora Gmbh	Molécules organiques pour dispositifs optoélectroniques
WO2021228114A1 (fr) *	2020-05-14	2021-11-18	季华实验室	Composé bore-azote, composition à électroluminescence organique et dispositif électroluminescent organique les comprenant
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CN115298187A (zh) *	2020-03-17	2022-11-04	默克专利有限公司	用于有机电致发光器件的杂芳族化合物
WO2023104285A1 (fr) *	2021-12-07	2023-06-15	Huawei Technologies Co., Ltd.	Composé émetteur hydrocarbure aromatique polycyclique dopé au bore (b-pah) et procédé de synthèse de b-pah
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2018
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CN114026101A (zh) *	2019-04-26	2022-02-08	出光兴产株式会社	多环化合物和包含多环化合物或组合物的有机电致发光器件
WO2020217229A1 (fr)	2019-04-26	2020-10-29	Idemitsu Kosan Co., Ltd.	Composé polycyclique et dispositif électroluminescent organique comprenant le composé polycyclique ou une composition
WO2021020929A1 (fr) *	2019-08-01	2021-02-04	주식회사 엘지화학	Composé et dispositif électroluminescent organique le comprenant
CN113544136B (zh) *	2019-08-01	2024-04-05	株式会社Lg化学	化合物和包含其的有机发光器件
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CN111333671A (zh) *	2020-03-16	2020-06-26	清华大学	一种发光材料及其应用以及包含其的有机电致发光器件
CN115298187A (zh) *	2020-03-17	2022-11-04	默克专利有限公司	用于有机电致发光器件的杂芳族化合物
WO2021228114A1 (fr) *	2020-05-14	2021-11-18	季华实验室	Composé bore-azote, composition à électroluminescence organique et dispositif électroluminescent organique les comprenant
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WO2023104285A1 (fr) *	2021-12-07	2023-06-15	Huawei Technologies Co., Ltd.	Composé émetteur hydrocarbure aromatique polycyclique dopé au bore (b-pah) et procédé de synthèse de b-pah
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