CA3016789A1 - Molecules organiques, destinees en particulier aux dispositifs optoelectroniques - Google Patents
Molecules organiques, destinees en particulier aux dispositifs optoelectroniques Download PDFInfo
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- CA3016789A1 CA3016789A1 CA3016789A CA3016789A CA3016789A1 CA 3016789 A1 CA3016789 A1 CA 3016789A1 CA 3016789 A CA3016789 A CA 3016789A CA 3016789 A CA3016789 A CA 3016789A CA 3016789 A1 CA3016789 A1 CA 3016789A1
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- 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
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
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- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 6
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- 229910052736 halogen Inorganic materials 0.000 claims description 5
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- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 230000005669 field effect Effects 0.000 claims description 4
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- 125000004076 pyridyl group Chemical group 0.000 claims description 4
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- 238000000295 emission spectrum Methods 0.000 description 12
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- 125000005069 octynyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C#C* 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102017121106.3 | 2017-09-12 | ||
| DE102017121106 | 2017-09-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA3016789A1 true CA3016789A1 (fr) | 2019-03-12 |
Family
ID=65721725
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA3016789A Pending CA3016789A1 (fr) | 2017-09-12 | 2018-09-07 | Molecules organiques, destinees en particulier aux dispositifs optoelectroniques |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA3016789A1 (fr) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| CN114075229A (zh) * | 2020-08-20 | 2022-02-22 | 江苏三月科技股份有限公司 | 一种含硼有机化合物及其在有机电致发光器件上的应用 |
| 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 |
-
2018
- 2018-09-07 CA CA3016789A patent/CA3016789A1/fr active Pending
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| 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 |
| WO2021020929A1 (fr) * | 2019-08-01 | 2021-02-04 | 주식회사 엘지화학 | Composé et dispositif électroluminescent organique le comprenant |
| CN113544136A (zh) * | 2019-08-01 | 2021-10-22 | 株式会社Lg化学 | 化合物和包含其的有机发光器件 |
| 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 |
| WO2021122757A1 (fr) * | 2019-12-20 | 2021-06-24 | Cynora Gmbh | Molécules organiques pour dispositifs optoélectroniques |
| 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 |
| CN111333671B (zh) * | 2020-03-16 | 2022-12-23 | 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 |
| 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 |
| CN114075229A (zh) * | 2020-08-20 | 2022-02-22 | 江苏三月科技股份有限公司 | 一种含硼有机化合物及其在有机电致发光器件上的应用 |
| 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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