JP2017501144A5 - - Google Patents
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- JP2017501144A5 JP2017501144A5 JP2016536844A JP2016536844A JP2017501144A5 JP 2017501144 A5 JP2017501144 A5 JP 2017501144A5 JP 2016536844 A JP2016536844 A JP 2016536844A JP 2016536844 A JP2016536844 A JP 2016536844A JP 2017501144 A5 JP2017501144 A5 JP 2017501144A5
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- Prior art keywords
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- aromatic ring
- branched
- Prior art date
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- 125000003118 aryl group Chemical group 0.000 claims description 50
- 125000004432 carbon atom Chemical group C* 0.000 claims description 42
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 13
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 20
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 17
- 239000000463 material Substances 0.000 claims 9
- 150000003254 radicals Chemical class 0.000 claims 8
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims 6
- 239000000203 mixture Substances 0.000 claims 5
- 239000000178 monomer Substances 0.000 claims 3
- 125000004429 atom Chemical group 0.000 claims 2
- 230000000903 blocking effect Effects 0.000 claims 2
- 238000005401 electroluminescence Methods 0.000 claims 2
- 230000005525 hole transport Effects 0.000 claims 2
- 239000010410 layer Substances 0.000 claims 2
- 239000011159 matrix material Substances 0.000 claims 2
- 206010012438 Dermatitis atopic Diseases 0.000 claims 1
- 206010061218 Inflammation Diseases 0.000 claims 1
- 206010023126 Jaundice Diseases 0.000 claims 1
- 206010023138 Jaundice neonatal Diseases 0.000 claims 1
- 201000006346 Neonatal Jaundice Diseases 0.000 claims 1
- 208000002193 Pain Diseases 0.000 claims 1
- 201000004681 Psoriasis Diseases 0.000 claims 1
- 206010047642 Vitiligo Diseases 0.000 claims 1
- 201000008937 atopic dermatitis Diseases 0.000 claims 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims 1
- 239000004020 conductor Substances 0.000 claims 1
- 239000002019 doping agent Substances 0.000 claims 1
- 230000005684 electric field Effects 0.000 claims 1
- 230000005669 field effect Effects 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 230000004054 inflammatory process Effects 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 239000007791 liquid phase Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 239000012044 organic layer Substances 0.000 claims 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 1
- 238000001126 phototherapy Methods 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 125000005650 substituted phenylene group Chemical group 0.000 claims 1
- 239000010409 thin film Substances 0.000 claims 1
- 238000001947 vapour-phase growth Methods 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 125000004001 thioalkyl group Chemical group 0.000 description 6
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 0 **C(*)(c(c-1c(*)c(*)c2*)c2N)c2c-1c(N)c(*)c(*)c2N Chemical compound **C(*)(c(c-1c(*)c(*)c2*)c2N)c2c-1c(N)c(*)c(*)c2N 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
- 125000005017 substituted alkenyl group Chemical group 0.000 description 2
- ICPSWZFVWAPUKF-UHFFFAOYSA-N 1,1'-spirobi[fluorene] Chemical compound C1=CC=C2C=C3C4(C=5C(C6=CC=CC=C6C=5)=CC=C4)C=CC=C3C2=C1 ICPSWZFVWAPUKF-UHFFFAOYSA-N 0.000 description 1
- HBXNJRXRZXNRMX-CYBMUJFWSA-N C[C@H]1C(c2c3[o]c(cccc4)c4c3ccc2)=CC=CC1 Chemical compound C[C@H]1C(c2c3[o]c(cccc4)c4c3ccc2)=CC=CC1 HBXNJRXRZXNRMX-CYBMUJFWSA-N 0.000 description 1
- VTKMFJSESAHMLR-UHFFFAOYSA-N Cc(cc1)cc2c1[o]c1c2cccc1 Chemical compound Cc(cc1)cc2c1[o]c1c2cccc1 VTKMFJSESAHMLR-UHFFFAOYSA-N 0.000 description 1
- QMHZGKUYNPVSLS-UHFFFAOYSA-N Cc(cc1)ccc1-c1c2[o]c(cccc3)c3c2ccc1 Chemical compound Cc(cc1)ccc1-c1c2[o]c(cccc3)c3c2ccc1 QMHZGKUYNPVSLS-UHFFFAOYSA-N 0.000 description 1
- GQMXKCYNCFQHKQ-UHFFFAOYSA-N Cc(cc1)ccc1-c1ccc2[o]c(cccc3)c3c2c1 Chemical compound Cc(cc1)ccc1-c1ccc2[o]c(cccc3)c3c2c1 GQMXKCYNCFQHKQ-UHFFFAOYSA-N 0.000 description 1
- DGRSXAREJHBDJB-UHFFFAOYSA-N Cc(cccc1)c1-c1ccc2[o]c(cccc3)c3c2c1 Chemical compound Cc(cccc1)c1-c1ccc2[o]c(cccc3)c3c2c1 DGRSXAREJHBDJB-UHFFFAOYSA-N 0.000 description 1
- GMDVCIYBQIBPAK-UHFFFAOYSA-N Cc1cccc(-c2ccc3[o]c4ccccc4c3c2)c1 Chemical compound Cc1cccc(-c2ccc3[o]c4ccccc4c3c2)c1 GMDVCIYBQIBPAK-UHFFFAOYSA-N 0.000 description 1
- OLWCXPIFHHTCDG-UHFFFAOYSA-N Cc1cccc2c1[o]c1c2cccc1-c1ccccc1 Chemical compound Cc1cccc2c1[o]c1c2cccc1-c1ccccc1 OLWCXPIFHHTCDG-UHFFFAOYSA-N 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- RSCFTWWOSOBAQS-UHFFFAOYSA-N c(cc12)ccc1[o]c1c2[I]=CC=C1 Chemical compound c(cc12)ccc1[o]c1c2[I]=CC=C1 RSCFTWWOSOBAQS-UHFFFAOYSA-N 0.000 description 1
- 125000005553 heteroaryloxy group Chemical group 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 150000003413 spiro compounds Chemical class 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13005697 | 2013-12-06 | ||
| EP13005697.1 | 2013-12-06 | ||
| PCT/EP2014/003148 WO2015082056A1 (de) | 2013-12-06 | 2014-11-26 | Verbindungen und organische elektronische vorrichtungen |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019147078A Division JP7114530B2 (ja) | 2013-12-06 | 2019-08-09 | 化合物および有機電子素子 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017501144A JP2017501144A (ja) | 2017-01-12 |
| JP2017501144A5 true JP2017501144A5 (OSRAM) | 2020-12-17 |
| JP6896422B2 JP6896422B2 (ja) | 2021-06-30 |
Family
ID=49758976
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016536844A Active JP6896422B2 (ja) | 2013-12-06 | 2014-11-26 | 化合物および有機電子素子 |
| JP2019147078A Active JP7114530B2 (ja) | 2013-12-06 | 2019-08-09 | 化合物および有機電子素子 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019147078A Active JP7114530B2 (ja) | 2013-12-06 | 2019-08-09 | 化合物および有機電子素子 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US10355217B2 (OSRAM) |
| EP (3) | EP3693437B1 (OSRAM) |
| JP (2) | JP6896422B2 (OSRAM) |
| KR (4) | KR102445509B1 (OSRAM) |
| CN (1) | CN105980518B (OSRAM) |
| TW (1) | TWI679188B (OSRAM) |
| WO (1) | WO2015082056A1 (OSRAM) |
Families Citing this family (82)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6896422B2 (ja) | 2013-12-06 | 2021-06-30 | メルク パテント ゲーエムベーハー | 化合物および有機電子素子 |
| TW201542500A (zh) * | 2013-12-26 | 2015-11-16 | 羅門哈斯電子材料韓國公司 | 有機電場發光化合物及包含該化合物之有機電場發光裝置 |
| US10944057B2 (en) | 2014-07-11 | 2021-03-09 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence devices, organic electroluminescence device, and electronic equipment |
| EP2978040B1 (en) * | 2014-07-22 | 2017-12-27 | Samsung Display Co., Ltd. | Organic light-emitting device |
| JP2017531628A (ja) | 2014-09-25 | 2017-10-26 | メルク パテント ゲーエムベーハー | ベンゾ［ｃ］クマリン構造をもつヘテロ環化合物 |
| KR102338908B1 (ko) | 2015-03-03 | 2021-12-14 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| EP3297978B1 (en) * | 2015-05-18 | 2020-04-01 | Merck Patent GmbH | Materials for organic electroluminescent devices |
| WO2016204151A1 (ja) | 2015-06-16 | 2016-12-22 | 出光興産株式会社 | 化合物、有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子及び電子機器 |
| KR102591635B1 (ko) | 2015-10-27 | 2023-10-20 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| KR102399570B1 (ko) | 2015-11-26 | 2022-05-19 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| CN107093675B (zh) * | 2015-12-23 | 2022-05-03 | 三星显示有限公司 | 有机发光器件 |
| US11910707B2 (en) | 2015-12-23 | 2024-02-20 | Samsung Display Co., Ltd. | Organic light-emitting device |
| CN106920896A (zh) * | 2015-12-23 | 2017-07-04 | 三星显示有限公司 | 有机发光器件 |
| JP7051691B2 (ja) | 2016-02-05 | 2022-04-11 | メルク パテント ゲーエムベーハー | 電子素子のための材料 |
| GB2547645A (en) | 2016-02-22 | 2017-08-30 | Cambridge Display Tech Ltd | Compound,composition and organic light-emitting device |
| KR20170127101A (ko) | 2016-05-10 | 2017-11-21 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| GB2554404A (en) * | 2016-09-26 | 2018-04-04 | Sumitomo Chemical Co | Solvent systems for preparation of photosensitive organic electronic devices |
| TWI764942B (zh) | 2016-10-10 | 2022-05-21 | 德商麥克專利有限公司 | 電子裝置 |
| KR102673970B1 (ko) | 2016-10-13 | 2024-06-11 | 삼성디스플레이 주식회사 | 유기발광 표시장치 그 제조방법 |
| KR102650409B1 (ko) * | 2016-10-20 | 2024-03-25 | 주식회사 동진쎄미켐 | 신규 화합물 및 이를 포함하는 유기 발광 소자 |
| CN107963973B (zh) * | 2016-10-20 | 2023-07-25 | 东进世美肯株式会社 | 新颖化合物及包含其的有机发光器件 |
| TWI745467B (zh) | 2016-11-02 | 2021-11-11 | 德商麥克專利有限公司 | 電子裝置用的材料 |
| EP3538535A1 (en) | 2016-11-08 | 2019-09-18 | Merck Patent GmbH | Compounds for electronic devices |
| TW201833118A (zh) | 2016-11-22 | 2018-09-16 | 德商麥克專利有限公司 | 用於電子裝置之材料 |
| KR102683465B1 (ko) | 2017-02-02 | 2024-07-09 | 메르크 파텐트 게엠베하 | 전자 디바이스용 재료 |
| EP3589624A1 (de) | 2017-03-02 | 2020-01-08 | Merck Patent GmbH | Materialien für organische elektronische vorrichtungen |
| KR102785888B1 (ko) * | 2017-04-17 | 2025-03-25 | 주식회사 동진쎄미켐 | 신규 화합물 및 이를 포함하는 유기 발광 소자 |
| US11649249B2 (en) | 2017-04-25 | 2023-05-16 | Merck Patent Gmbh | Compounds for electronic devices |
| US20200136045A1 (en) | 2017-06-28 | 2020-04-30 | Merck Patent Gmbh | Materials for electronic devices |
| TWI779067B (zh) | 2017-07-28 | 2022-10-01 | 德商麥克專利有限公司 | 電子裝置用材料 |
| KR102746068B1 (ko) | 2017-09-08 | 2024-12-24 | 메르크 파텐트 게엠베하 | 전자 디바이스용 재료 |
| US11832513B2 (en) | 2017-11-23 | 2023-11-28 | Merck Patent Gmbh | Materials for electronic devices |
| KR20240025066A (ko) * | 2017-12-15 | 2024-02-26 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 치환된 방향족 아민 |
| CN109928961B (zh) * | 2017-12-15 | 2021-06-15 | 广东阿格蕾雅光电材料有限公司 | 含有4-硫砜芳基二苯并呋喃的光电材料及应用 |
| CN111819167A (zh) | 2018-03-16 | 2020-10-23 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
| EP3775099B1 (de) * | 2018-04-04 | 2022-08-24 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
| KR102559633B1 (ko) * | 2018-05-31 | 2023-08-02 | 주식회사 동진쎄미켐 | 신규 화합물 및 이를 포함하는 유기발광 소자 |
| KR102628804B1 (ko) * | 2018-07-10 | 2024-01-24 | 주식회사 동진쎄미켐 | 신규 화합물 및 이를 포함하는 유기발광 소자 |
| JP6866333B2 (ja) | 2018-08-16 | 2021-04-28 | エルジー・ケム・リミテッド | ４又は５位に芳香族アミノ基が置換したフルオレン誘導体を繰り返し単位として主鎖に含むポリマー、その正孔輸送材料としての使用、並びにそれを含む有機電子デバイス |
| CN110903276A (zh) * | 2018-09-17 | 2020-03-24 | 北京鼎材科技有限公司 | 有机化合物及有机电致发光器件 |
| JP7728702B2 (ja) | 2018-12-20 | 2025-08-25 | メルク パテント ゲーエムベーハー | 電子デバイス用の材料 |
| US12069950B2 (en) * | 2018-12-20 | 2024-08-20 | Merck Kgaa | Materials for electronic devices |
| KR102041137B1 (ko) * | 2019-04-02 | 2019-11-07 | 머티어리얼사이언스 주식회사 | 유기 화합물 및 이를 포함하는 유기전계발광소자 |
| TW202110788A (zh) | 2019-05-03 | 2021-03-16 | 德商麥克專利有限公司 | 電子裝置 |
| TW202110789A (zh) | 2019-05-03 | 2021-03-16 | 德商麥克專利有限公司 | 電子裝置 |
| EP3790857B1 (en) | 2019-06-28 | 2023-01-11 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element and electronic device |
| EP4041709A1 (de) * | 2019-10-11 | 2022-08-17 | Merck Patent GmbH | Verbindungen für elektronische vorrichtungen |
| CN114207863B (zh) * | 2020-01-23 | 2025-03-28 | 株式会社Lg化学 | 有机发光器件 |
| KR20210117219A (ko) * | 2020-03-18 | 2021-09-28 | 에스에프씨 주식회사 | 다환 방향족 유도체 화합물을 이용한 유기발광소자 |
| WO2021187923A1 (ko) * | 2020-03-18 | 2021-09-23 | 에스에프씨 주식회사 | 다환 방향족 유도체 화합물을 이용한 유기발광소자 |
| KR102599003B1 (ko) | 2020-04-20 | 2023-11-03 | 삼성에스디아이 주식회사 | 유기 광전자 소자용 조성물, 유기 광전자 소자 및 표시 장치 |
| KR102870803B1 (ko) | 2020-08-20 | 2025-10-14 | 삼성디스플레이 주식회사 | 아민 화합물 및 이를 포함한 발광 소자 |
| KR20230118991A (ko) * | 2020-12-18 | 2023-08-14 | 메르크 파텐트 게엠베하 | 전자 디바이스용 재료 |
| CN115109018A (zh) * | 2021-03-19 | 2022-09-27 | 烟台显华科技集团股份有限公司 | 一种芴双取代芳胺化合物及其应用 |
| WO2023052275A1 (de) | 2021-09-28 | 2023-04-06 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
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| CN119212975A (zh) * | 2022-05-18 | 2024-12-27 | 出光兴产株式会社 | 化合物、有机电致发光元件用材料、有机电致发光元件、和电子设备 |
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2014
- 2014-11-26 JP JP2016536844A patent/JP6896422B2/ja active Active
- 2014-11-26 US US15/101,193 patent/US10355217B2/en active Active
- 2014-11-26 CN CN201480066007.1A patent/CN105980518B/zh active Active
- 2014-11-26 EP EP20160631.6A patent/EP3693437B1/de active Active
- 2014-11-26 EP EP18157771.9A patent/EP3345984B1/de active Active
- 2014-11-26 KR KR1020177023410A patent/KR102445509B1/ko active Active
- 2014-11-26 EP EP14808490.8A patent/EP3077477B1/de active Active
- 2014-11-26 KR KR1020167016183A patent/KR101772371B1/ko not_active Ceased
- 2014-11-26 KR KR1020217037600A patent/KR102616941B1/ko active Active
- 2014-11-26 WO PCT/EP2014/003148 patent/WO2015082056A1/de not_active Ceased
- 2014-11-26 KR KR1020237043761A patent/KR20240005971A/ko active Pending
- 2014-12-03 TW TW103141982A patent/TWI679188B/zh active
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2019
- 2019-05-30 US US16/426,042 patent/US11056652B2/en active Active
- 2019-08-09 JP JP2019147078A patent/JP7114530B2/ja active Active
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