JP2010143879A - ジアセナフト[1,2−b:1’,2’−k]クリセン誘導体 - Google Patents
ジアセナフト[1,2−b:1’,2’−k]クリセン誘導体 Download PDFInfo
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- JP2010143879A JP2010143879A JP2008324468A JP2008324468A JP2010143879A JP 2010143879 A JP2010143879 A JP 2010143879A JP 2008324468 A JP2008324468 A JP 2008324468A JP 2008324468 A JP2008324468 A JP 2008324468A JP 2010143879 A JP2010143879 A JP 2010143879A
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- FAAAKDIORRDGMS-UHFFFAOYSA-N Brc1cc2c(cccc3)c3ccc2c2ccccc12 Chemical compound Brc1cc2c(cccc3)c3ccc2c2ccccc12 FAAAKDIORRDGMS-UHFFFAOYSA-N 0.000 description 1
- MGACHYZJCYWHPI-UHFFFAOYSA-N C(C1)C=CC=C1Nc1ccccc1 Chemical compound C(C1)C=CC=C1Nc1ccccc1 MGACHYZJCYWHPI-UHFFFAOYSA-N 0.000 description 1
- PVARTZPEJXNIBD-UHFFFAOYSA-N C(CC=CC1)C1N(c1ccccc1)c1cc(c2ccccc2cc2)c2c2c1cccc2 Chemical compound C(CC=CC1)C1N(c1ccccc1)c1cc(c2ccccc2cc2)c2c2c1cccc2 PVARTZPEJXNIBD-UHFFFAOYSA-N 0.000 description 1
- ZVPHXMGYAYMXAP-UHFFFAOYSA-N C(c1ccccc1)c1c(cc(C2=CC(C3)C3C3C=CC=C4C23)c4c2)c2c(ccc(c2c3)cc(C4=CCC5)c3-c3c4c5ccc3)c2c1 Chemical compound C(c1ccccc1)c1c(cc(C2=CC(C3)C3C3C=CC=C4C23)c4c2)c2c(ccc(c2c3)cc(C4=CCC5)c3-c3c4c5ccc3)c2c1 ZVPHXMGYAYMXAP-UHFFFAOYSA-N 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N C(c1ccccc1)c1ccccc1 Chemical compound C(c1ccccc1)c1ccccc1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- FURHMGVKKGEGMZ-UHFFFAOYSA-N Ic1cccc2cccc(I)c12 Chemical compound Ic1cccc2cccc(I)c12 FURHMGVKKGEGMZ-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Nc1ccccc1 Chemical compound Nc1ccccc1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
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Abstract
【解決手段】 ジアセナフト[1,2−b:1’,2’−k]クリセン誘導体であることを特徴とする有機化合物。
【選択図】 図5
Description
メチル基、エチル基、プロピル基などのアルキル基、
ベンジル基などのアラルキル基、
フェニル基、ビフェニル基などのアリール基、
ピリジル基、ピロリル基などの複素環基、
ジメチルアミノ基、ジエチルアミノ基、ジベンジルアミノ基、ジフェニルアミノ基、ジトリルアミノ基などのアミノ基、
メトキシル基、エトキシル基、プロポキシル基、フェノキシル基などのアルコキシル基、
シアノ基、フッ素、塩素、臭素、ヨウ素などのハロゲン原子などが挙げられるが、もちろんこれらに限定されるものではない。
1つめに振動子強度が高いこと
2つめに発光にかかわる骨格の振動部分が少ないこと
があげられる。これら2点の条件の何れもが満たされることが重要であると本発明者等は考える。
1.発光層内での電子・ホールの輸送。
2.ホスト材料の励起子生成。
3.ホスト材料同士の分子間の励起エネルギー伝達。
4.ホスト材料からゲスト材料への励起エネルギー移動。
例示化合物A3の、1×10−5mol/lにおけるトルエン溶液の発光スペクトルは、日立製F−4500を用い、350nmの励起波長においてフォトルミネッセンスの測定を行った結果、459nmに最大強度を有するスペクトルであった。
[例示化合物A1の合成]
実施例2に用いられる原料のクリセンをE4に変更する以外は同様にして合成した。
[例示化合物A1の合成]
実施例2に用いられる原料のクリセンをE5に変更する以外は同様にして合成した。
本実施例では、多層型有機発光素子の第五の例で示した素子(陽極/ホール注入層/ホール輸送層/発光層/ホール・エキシトンブロッキング層/電子輸送層/陰極)とした。ガラス基板上に100nmのITOをパターニングした。そのITO基板上に、以下の有機層と電極層を10−5Paの真空チャンバー内で抵抗加熱による真空蒸着して連続製膜し、対向する電極面積が3mm2になるようにした。
ホール輸送層(30nm) F−1
発光層(30nm) ホストF−2、ゲスト:例示化合物 (重量比 5%)
ホール・エキシトンブロッキング層(10nm) F−3
電子輸送層(30nm) F−4
金属電極層1(1nm) LiF
金属電極層2(100nm) Al
2,15 画素回路
11 走査信号ドライバー
12 情報信号ドライバー
13 電流供給源
14 画素
21 第一の薄膜トランジスタ(TFT)
22 コンデンサー(Cadd)
23 第二の薄膜トランジスタ(TFT)
31 基板
32 防湿層
33 ゲート電極
34 ゲート絶縁膜
35 半導体膜
36 ドレイン電極
37 ソース電極
38 TFT素子
39 絶縁膜
310 コンタクトホール(スルーホール)
311 陽極
312 有機層
313 陰極
314 第一の保護層
315 第二の保護層
Claims (2)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008324468A JP5424635B2 (ja) | 2008-12-19 | 2008-12-19 | ジアセナフト[1,2−b:1’,2’−k]クリセン誘導体 |
EP09833525.0A EP2379473B1 (en) | 2008-12-19 | 2009-12-16 | Diacenaphtho[1,2-b:1',2'-k]chrysene derivative |
US13/140,809 US8951648B2 (en) | 2008-12-19 | 2009-12-16 | Diacenaphtho[1,2-b:1′,2′-k]chrysene derivative |
CN200980150383.8A CN102245546B (zh) | 2008-12-19 | 2009-12-16 | 二苊并[1,2-b:1',2'-k]*衍生物 |
KR1020117016034A KR101309339B1 (ko) | 2008-12-19 | 2009-12-16 | 디아세나프토[1,2-b:1',2'-k]크리센 유도체 |
CN201410146622.5A CN103952144B (zh) | 2008-12-19 | 2009-12-16 | 二苊并[1,2-b:1’,2’-k]*衍生物 |
PCT/JP2009/071367 WO2010071224A1 (en) | 2008-12-19 | 2009-12-16 | DIACENAPHTHO[1,2-b:1',2'-k]CHRYSENE DERIVATIVE |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008324468A JP5424635B2 (ja) | 2008-12-19 | 2008-12-19 | ジアセナフト[1,2−b:1’,2’−k]クリセン誘導体 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2010143879A true JP2010143879A (ja) | 2010-07-01 |
JP5424635B2 JP5424635B2 (ja) | 2014-02-26 |
Family
ID=42268889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2008324468A Active JP5424635B2 (ja) | 2008-12-19 | 2008-12-19 | ジアセナフト[1,2−b:1’,2’−k]クリセン誘導体 |
Country Status (6)
Country | Link |
---|---|
US (1) | US8951648B2 (ja) |
EP (1) | EP2379473B1 (ja) |
JP (1) | JP5424635B2 (ja) |
KR (1) | KR101309339B1 (ja) |
CN (2) | CN102245546B (ja) |
WO (1) | WO2010071224A1 (ja) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011040631A1 (en) * | 2009-10-01 | 2011-04-07 | Canon Kabushiki Kaisha | Diindenopicene compound and organic light emitting device using the same |
WO2011102102A1 (en) * | 2010-02-16 | 2011-08-25 | Canon Kabushiki Kaisha | Novel organic compound and organic light-emitting device |
WO2016204150A1 (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 |
DE102019108200A1 (de) | 2018-03-30 | 2019-10-02 | Canon Kabushiki Kaisha | Organisches Lichtemissionsbauelement, Anzeigegerät, Bildaufnahmegerät und Beleuchtungsgerät |
WO2020039708A1 (ja) | 2018-08-23 | 2020-02-27 | 国立大学法人九州大学 | 有機エレクトロルミネッセンス素子 |
US20210036232A1 (en) * | 2019-08-02 | 2021-02-04 | Canon Kabushiki Kaisha | Organic compound, organic light-emitting device, display device, photoelectric conversion apparatus, electronic apparatus, lighting device, and movable body |
EP3800180A1 (en) | 2019-10-03 | 2021-04-07 | Canon Kabushiki Kaisha | Organic compound, organic light-emitting element, display apparatus, image pickup apparatus, lighting apparatus, and moving object |
JP2021059523A (ja) * | 2019-10-03 | 2021-04-15 | キヤノン株式会社 | 有機化合物、有機発光素子、表示装置、撮像装置、照明装置、移動体 |
EP3967675A1 (en) | 2020-09-11 | 2022-03-16 | Canon Kabushiki Kaisha | Diacephenanthryleno chrysene derivatives for use in organic light-emitting devices |
US11964930B2 (en) | 2019-11-07 | 2024-04-23 | Canon Kabushiki Kaisha | Organic compound and organic light-emitting element |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5561929B2 (ja) | 2008-12-19 | 2014-07-30 | キヤノン株式会社 | 新規有機化合物 |
JP6016511B2 (ja) * | 2012-08-07 | 2016-10-26 | キヤノン株式会社 | 新規縮合多環化合物、それを有する有機発光素子、表示装置、画像情報処理装置、照明装置及び画像形成装置 |
US9200365B2 (en) * | 2012-08-15 | 2015-12-01 | Applied Material, Inc. | Method of catalytic film deposition |
US11844268B2 (en) | 2019-11-12 | 2023-12-12 | Canon Kabushiki Kaisha | Organic compound and organic light-emitting element |
Citations (6)
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JPH10294177A (ja) * | 1997-04-17 | 1998-11-04 | Mitsui Chem Inc | 有機電界発光素子 |
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Also Published As
Publication number | Publication date |
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EP2379473B1 (en) | 2017-02-22 |
KR20110104026A (ko) | 2011-09-21 |
CN103952144B (zh) | 2016-08-17 |
CN102245546A (zh) | 2011-11-16 |
EP2379473A4 (en) | 2012-07-04 |
JP5424635B2 (ja) | 2014-02-26 |
US20110251446A1 (en) | 2011-10-13 |
EP2379473A1 (en) | 2011-10-26 |
CN103952144A (zh) | 2014-07-30 |
WO2010071224A1 (en) | 2010-06-24 |
KR101309339B1 (ko) | 2013-09-17 |
US8951648B2 (en) | 2015-02-10 |
CN102245546B (zh) | 2015-05-13 |
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