KR20220157948A - 페난트롤린 유도체의 결정 및 그 제조 방법, 그리고 그것을 사용한 발광 소자 - Google Patents
페난트롤린 유도체의 결정 및 그 제조 방법, 그리고 그것을 사용한 발광 소자 Download PDFInfo
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- KR20220157948A KR20220157948A KR1020227031056A KR20227031056A KR20220157948A KR 20220157948 A KR20220157948 A KR 20220157948A KR 1020227031056 A KR1020227031056 A KR 1020227031056A KR 20227031056 A KR20227031056 A KR 20227031056A KR 20220157948 A KR20220157948 A KR 20220157948A
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- 150000003216 pyrazines Chemical class 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000005581 pyrene group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 1
- 150000003230 pyrimidines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 150000004322 quinolinols Chemical class 0.000 description 1
- 150000004059 quinone derivatives Chemical class 0.000 description 1
- 230000009467 reduction 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
- 239000004065 semiconductor Substances 0.000 description 1
- 150000003377 silicon compounds Chemical group 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000037 tert-butyldiphenylsilyl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1[Si]([H])([*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- PCCVSPMFGIFTHU-UHFFFAOYSA-N tetracyanoquinodimethane Chemical class N#CC(C#N)=C1C=CC(=C(C#N)C#N)C=C1 PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 125000001544 thienyl group Chemical group 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
- 125000003944 tolyl group Chemical group 0.000 description 1
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- H01L51/0072—
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/10—Apparatus or processes specially adapted to the manufacture of electroluminescent light sources
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Materials Engineering (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
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| Application Number | Priority Date | Filing Date | Title |
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| JP2020055829 | 2020-03-26 | ||
| JPJP-P-2020-055829 | 2020-03-26 | ||
| PCT/JP2021/012518 WO2021193818A1 (ja) | 2020-03-26 | 2021-03-25 | フェナントロリン誘導体の結晶およびその製造方法ならびにそれを用いた発光素子 |
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| KR20220157948A true KR20220157948A (ko) | 2022-11-29 |
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| JP (1) | JPWO2021193818A1 (ja) |
| KR (1) | KR20220157948A (ja) |
| CN (1) | CN115335385A (ja) |
| WO (1) | WO2021193818A1 (ja) |
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| CN114195809B (zh) * | 2021-12-27 | 2023-11-14 | 中国科学院长春应用化学研究所 | 一种硼杂或磷杂稠环化合物及其制备方法和应用 |
| WO2023190159A1 (ja) * | 2022-04-01 | 2023-10-05 | 東レ株式会社 | 化合物、それを用いた発光素子材料および発光素子、光電変換素子材料、色変換組成物、色変換シート、光源ユニット、表示装置、照明装置 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004281390A (ja) | 2003-02-25 | 2004-10-07 | Toray Ind Inc | 発光素子用材料、及びこれを含む発光素子 |
| JP2008189660A (ja) | 2007-01-11 | 2008-08-21 | Toray Ind Inc | 含窒素芳香環誘導体の製造方法 |
| WO2015156228A1 (ja) | 2014-04-07 | 2015-10-15 | 東レ株式会社 | 高分子電解質組成物ならびにそれを用いた高分子電解質膜、膜電極複合体および固体高分子形燃料電池 |
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| JP4710268B2 (ja) * | 2003-07-23 | 2011-06-29 | 東レ株式会社 | ピロメテン化合物、それを用いた発光素子材料ならびに発光素子 |
| WO2006021982A1 (ja) * | 2004-08-23 | 2006-03-02 | Toray Industries, Inc. | 発光素子用材料および発光素子 |
| JP4842587B2 (ja) * | 2005-08-11 | 2011-12-21 | 株式会社半導体エネルギー研究所 | フェナントロリン誘導体化合物、並びにそれを利用する電子輸送性材料、発光素子、発光装置及び電子機器 |
| CN101308906A (zh) * | 2007-05-16 | 2008-11-19 | 财团法人山形县产业技术振兴机构 | 电子输送性材料及使用该电子输送性材料的有机发光元件 |
| JP4784631B2 (ja) * | 2008-09-30 | 2011-10-05 | トヨタ自動車株式会社 | 駆動力伝達装置 |
| WO2010084852A1 (ja) * | 2009-01-23 | 2010-07-29 | 東レ株式会社 | 発光素子材料および発光素子 |
| WO2016121597A1 (ja) * | 2015-01-29 | 2016-08-04 | 東レ株式会社 | フェナントロリン誘導体、それを含有する電子デバイス、発光素子および光電変換素子 |
| CN110835351A (zh) * | 2018-08-15 | 2020-02-25 | 江苏三月光电科技有限公司 | 一种以吡咯亚甲基硼络合物为核心的有机化合物及其制备和应用 |
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2021
- 2021-03-25 CN CN202180023209.8A patent/CN115335385A/zh active Pending
- 2021-03-25 KR KR1020227031056A patent/KR20220157948A/ko unknown
- 2021-03-25 JP JP2021517490A patent/JPWO2021193818A1/ja active Pending
- 2021-03-25 WO PCT/JP2021/012518 patent/WO2021193818A1/ja active Application Filing
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004281390A (ja) | 2003-02-25 | 2004-10-07 | Toray Ind Inc | 発光素子用材料、及びこれを含む発光素子 |
| JP2008189660A (ja) | 2007-01-11 | 2008-08-21 | Toray Ind Inc | 含窒素芳香環誘導体の製造方法 |
| WO2015156228A1 (ja) | 2014-04-07 | 2015-10-15 | 東レ株式会社 | 高分子電解質組成物ならびにそれを用いた高分子電解質膜、膜電極複合体および固体高分子形燃料電池 |
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| Publication number | Publication date |
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| WO2021193818A1 (ja) | 2021-09-30 |
| CN115335385A (zh) | 2022-11-11 |
| JPWO2021193818A1 (ja) | 2021-09-30 |
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