CN113461548B - 一种芳香族胺类衍生物及其应用 - Google Patents
一种芳香族胺类衍生物及其应用 Download PDFInfo
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- CN113461548B CN113461548B CN202010242245.0A CN202010242245A CN113461548B CN 113461548 B CN113461548 B CN 113461548B CN 202010242245 A CN202010242245 A CN 202010242245A CN 113461548 B CN113461548 B CN 113461548B
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- layer
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- aromatic amine
- hole
- amine derivative
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- 150000004982 aromatic amines Chemical class 0.000 title claims abstract description 18
- 239000010410 layer Substances 0.000 claims description 106
- 239000000463 material Substances 0.000 claims description 48
- 230000005525 hole transport Effects 0.000 claims description 29
- 238000002347 injection Methods 0.000 claims description 26
- 239000007924 injection Substances 0.000 claims description 26
- 230000000903 blocking effect Effects 0.000 claims description 19
- 239000002346 layers by function Substances 0.000 claims description 10
- 239000011368 organic material Substances 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 abstract description 30
- 238000004770 highest occupied molecular orbital Methods 0.000 abstract description 10
- 230000002035 prolonged effect Effects 0.000 abstract description 5
- 239000004065 semiconductor Substances 0.000 abstract description 2
- 230000000052 comparative effect Effects 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 239000000376 reactant Substances 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- 238000007740 vapor deposition Methods 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 125000001624 naphthyl group Chemical group 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- ISMDILRWKSYCOD-GNKBHMEESA-N C(C1=CC=CC=C1)[C@@H]1NC(OCCCCCCCCCCCNC([C@@H](NC(C[C@@H]1O)=O)C(C)C)=O)=O Chemical compound C(C1=CC=CC=C1)[C@@H]1NC(OCCCCCCCCCCCNC([C@@H](NC(C[C@@H]1O)=O)C(C)C)=O)=O ISMDILRWKSYCOD-GNKBHMEESA-N 0.000 description 4
- 229940126639 Compound 33 Drugs 0.000 description 4
- -1 aromatic amine compounds Chemical class 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000008204 material by function Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 229910001873 dinitrogen Inorganic materials 0.000 description 3
- 239000007772 electrode material Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000005286 illumination Methods 0.000 description 3
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000006798 recombination Effects 0.000 description 3
- 238000005215 recombination Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000005070 sampling Methods 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 238000010025 steaming Methods 0.000 description 3
- 238000003756 stirring Methods 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
- 238000009826 distribution Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000004957 naphthylene group Chemical group 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000208125 Nicotiana Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000011982 device technology Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000000113 differential scanning calorimetry Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000000295 emission spectrum Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000012994 industrial processing Methods 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000001894 space-charge-limited current method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
- C07C211/60—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton containing a ring other than a six-membered aromatic ring forming part of at least one of the condensed ring systems
-
- 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]
- H10K50/14—Carrier transporting layers
- H10K50/15—Hole transporting layers
-
- 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]
- H10K50/17—Carrier injection layers
-
- 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]
- H10K50/18—Carrier blocking layers
-
- 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
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
-
- 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
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Optics & Photonics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims (4)
Priority Applications (1)
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CN202010242245.0A CN113461548B (zh) | 2020-03-31 | 2020-03-31 | 一种芳香族胺类衍生物及其应用 |
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CN202010242245.0A CN113461548B (zh) | 2020-03-31 | 2020-03-31 | 一种芳香族胺类衍生物及其应用 |
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CN113461548A CN113461548A (zh) | 2021-10-01 |
CN113461548B true CN113461548B (zh) | 2023-12-12 |
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Families Citing this family (1)
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CN115784904B (zh) * | 2022-09-14 | 2024-03-22 | 陕西莱特光电材料股份有限公司 | 含氮化合物和电子元件及电子装置 |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09194441A (ja) * | 1996-01-12 | 1997-07-29 | Idemitsu Kosan Co Ltd | ナフチル基を有するジアミン誘導体及び該誘導体を用いた有機エレクトロルミネッセンス素子 |
JP2003040844A (ja) * | 2001-07-30 | 2003-02-13 | Konica Corp | 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材料及びそれ等に用いる化合物 |
JP2009016719A (ja) * | 2007-07-09 | 2009-01-22 | Konica Minolta Holdings Inc | 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 |
CN101395126A (zh) * | 2006-03-07 | 2009-03-25 | 出光兴产株式会社 | 芳香族胺衍生物及使用其的有机电致发光元件 |
KR20100005903A (ko) * | 2008-07-08 | 2010-01-18 | 덕산하이메탈(주) | 페닐-나프틸 유도체 및 이를 사용하는 유기전계발광소자 |
CN105529405A (zh) * | 2014-10-17 | 2016-04-27 | 三星显示有限公司 | 有机发光元件 |
KR20170018627A (ko) * | 2015-08-10 | 2017-02-20 | (주)피엔에이치테크 | 유기발광 화합물을 포함하는 유기전계발광소자 |
KR20170127099A (ko) * | 2016-05-10 | 2017-11-21 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
CN108569970A (zh) * | 2017-10-19 | 2018-09-25 | 北京鼎材科技有限公司 | 联苯二胺型的三芳胺化合物及包含其的有机电致发光器件 |
KR20190124620A (ko) * | 2018-04-26 | 2019-11-05 | (주)피엔에이치테크 | 유기발광 화합물 및 이를 포함하는 유기전계발광소자 |
CN111138296A (zh) * | 2018-11-01 | 2020-05-12 | 东进世美肯株式会社 | 新型覆盖层用化合物及包含其的有机发光器件 |
-
2020
- 2020-03-31 CN CN202010242245.0A patent/CN113461548B/zh active Active
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH09194441A (ja) * | 1996-01-12 | 1997-07-29 | Idemitsu Kosan Co Ltd | ナフチル基を有するジアミン誘導体及び該誘導体を用いた有機エレクトロルミネッセンス素子 |
JP2003040844A (ja) * | 2001-07-30 | 2003-02-13 | Konica Corp | 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材料及びそれ等に用いる化合物 |
CN101395126A (zh) * | 2006-03-07 | 2009-03-25 | 出光兴产株式会社 | 芳香族胺衍生物及使用其的有机电致发光元件 |
JP2009016719A (ja) * | 2007-07-09 | 2009-01-22 | Konica Minolta Holdings Inc | 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 |
KR20100005903A (ko) * | 2008-07-08 | 2010-01-18 | 덕산하이메탈(주) | 페닐-나프틸 유도체 및 이를 사용하는 유기전계발광소자 |
CN105529405A (zh) * | 2014-10-17 | 2016-04-27 | 三星显示有限公司 | 有机发光元件 |
KR20170018627A (ko) * | 2015-08-10 | 2017-02-20 | (주)피엔에이치테크 | 유기발광 화합물을 포함하는 유기전계발광소자 |
KR20170127099A (ko) * | 2016-05-10 | 2017-11-21 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
CN108569970A (zh) * | 2017-10-19 | 2018-09-25 | 北京鼎材科技有限公司 | 联苯二胺型的三芳胺化合物及包含其的有机电致发光器件 |
KR20190124620A (ko) * | 2018-04-26 | 2019-11-05 | (주)피엔에이치테크 | 유기발광 화합물 및 이를 포함하는 유기전계발광소자 |
CN111138296A (zh) * | 2018-11-01 | 2020-05-12 | 东进世美肯株式会社 | 新型覆盖层用化合物及包含其的有机发光器件 |
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