KR102345329B1 - 조성물, 인광 발광성 화합물 및 발광 소자 - Google Patents
조성물, 인광 발광성 화합물 및 발광 소자 Download PDFInfo
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- KR102345329B1 KR102345329B1 KR1020207000602A KR20207000602A KR102345329B1 KR 102345329 B1 KR102345329 B1 KR 102345329B1 KR 1020207000602 A KR1020207000602 A KR 1020207000602A KR 20207000602 A KR20207000602 A KR 20207000602A KR 102345329 B1 KR102345329 B1 KR 102345329B1
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- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 125000005581 pyrene group Chemical group 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
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- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- IGLNJRXAVVLDKE-UHFFFAOYSA-N rubidium atom Chemical compound [Rb] IGLNJRXAVVLDKE-UHFFFAOYSA-N 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 238000007789 sealing Methods 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
- 229910000077 silane Inorganic materials 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000012419 sodium bis(2-methoxyethoxy)aluminum hydride Substances 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 238000000956 solid--liquid extraction Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910000080 stannane Inorganic materials 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- NLDYACGHTUPAQU-UHFFFAOYSA-N tetracyanoethylene Chemical group N#CC(C#N)=C(C#N)C#N NLDYACGHTUPAQU-UHFFFAOYSA-N 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 125000005580 triphenylene group Chemical group 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C07D233/58—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring nitrogen atoms
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0033—Iridium compounds
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0073—Rhodium compounds
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
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- H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
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- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
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- H10K85/346—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising platinum
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- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
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- Inorganic Chemistry (AREA)
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- Manufacturing & Machinery (AREA)
- Optics & Photonics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
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| Application Number | Priority Date | Filing Date | Title |
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| KR1020217042634A KR20220000988A (ko) | 2016-01-29 | 2017-01-24 | 조성물, 인광 발광성 화합물 및 발광 소자 |
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| JP2016015799 | 2016-01-29 | ||
| JPJP-P-2016-015799 | 2016-01-29 | ||
| PCT/JP2017/002377 WO2017130977A1 (ja) | 2016-01-29 | 2017-01-24 | 組成物、燐光発光性化合物及び発光素子 |
| KR1020187024128A KR102099524B1 (ko) | 2016-01-29 | 2017-01-24 | 조성물, 인광 발광성 화합물 및 발광 소자 |
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| KR1020217042634A Ceased KR20220000988A (ko) | 2016-01-29 | 2017-01-24 | 조성물, 인광 발광성 화합물 및 발광 소자 |
| KR1020187024128A Active KR102099524B1 (ko) | 2016-01-29 | 2017-01-24 | 조성물, 인광 발광성 화합물 및 발광 소자 |
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| KR1020187024128A Active KR102099524B1 (ko) | 2016-01-29 | 2017-01-24 | 조성물, 인광 발광성 화합물 및 발광 소자 |
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| WO2018088573A1 (ja) * | 2016-11-14 | 2018-05-17 | 住友化学株式会社 | 発光素子、並びに、それに用いる金属錯体及び組成物 |
| JP7191687B2 (ja) * | 2018-12-28 | 2022-12-19 | 住友化学株式会社 | 発光素子用組成物及びそれを含有する発光素子 |
| JP6585812B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585817B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585811B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585273B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585819B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6688869B1 (ja) * | 2018-12-28 | 2020-04-28 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585816B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6688870B1 (ja) * | 2018-12-28 | 2020-04-28 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585815B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP7191688B2 (ja) * | 2018-12-28 | 2022-12-19 | 住友化学株式会社 | 発光素子用組成物及びそれを含有する発光素子 |
| JP6585810B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585818B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585813B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6688871B1 (ja) * | 2018-12-28 | 2020-04-28 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP6585814B1 (ja) | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP7191686B2 (ja) * | 2018-12-28 | 2022-12-19 | 住友化学株式会社 | 発光素子用組成物及びそれを含有する発光素子 |
| JP6688872B1 (ja) * | 2018-12-28 | 2020-04-28 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
| JP7191685B2 (ja) * | 2018-12-28 | 2022-12-19 | 住友化学株式会社 | 発光素子用組成物及びそれを含有する発光素子 |
| JP7191684B2 (ja) * | 2018-12-28 | 2022-12-19 | 住友化学株式会社 | 発光素子用組成物及びそれを含有する発光素子 |
| JP6585272B1 (ja) * | 2018-12-28 | 2019-10-02 | 住友化学株式会社 | 発光素子用組成物及び発光素子の製造方法 |
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| JPWO2017130977A1 (ja) | 2018-02-08 |
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| WO2017130977A1 (ja) | 2017-08-03 |
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| US20190036046A1 (en) | 2019-01-31 |
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| EP3410508A4 (en) | 2019-07-17 |
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| JP2021120952A (ja) | 2021-08-19 |
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| CN108496259B (zh) | 2020-03-03 |
| KR102099524B1 (ko) | 2020-04-09 |
| US20200194695A1 (en) | 2020-06-18 |
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