JP2007091721A5 - - Google Patents

Download PDF

Info

Publication number
JP2007091721A5
JP2007091721A5 JP2006231489A JP2006231489A JP2007091721A5 JP 2007091721 A5 JP2007091721 A5 JP 2007091721A5 JP 2006231489 A JP2006231489 A JP 2006231489A JP 2006231489 A JP2006231489 A JP 2006231489A JP 2007091721 A5 JP2007091721 A5 JP 2007091721A5
Authority
JP
Japan
Prior art keywords
carbon atoms
group
anthracene derivative
hydrogen
represent
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2006231489A
Other languages
Japanese (ja)
Other versions
JP2007091721A (en
JP5041766B2 (en
Filing date
Publication date
Application filed filed Critical
Priority to JP2006231489A priority Critical patent/JP5041766B2/en
Priority claimed from JP2006231489A external-priority patent/JP5041766B2/en
Publication of JP2007091721A publication Critical patent/JP2007091721A/en
Publication of JP2007091721A5 publication Critical patent/JP2007091721A5/ja
Application granted granted Critical
Publication of JP5041766B2 publication Critical patent/JP5041766B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (21)

一般式(1)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。R4は炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。R5は炭素数6以上25以下のアリール基を表す。R6は炭素数6以上25以下のアリール基を表す。X1は炭素数6以上25以下のアリーレン基を表す。)
An anthracene derivative represented by the general formula (1).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. R 4 represents either an alkyl group having 1 to 4 carbon atoms or an aryl group having 6 to 25 carbon atoms, R 5 represents an aryl group having 6 to 25 carbon atoms, R 6 represents an aryl group having 6 to 25 carbon atoms, and X 1 represents an arylene group having 6 to 25 carbon atoms.
一般式(2)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。R5は炭素数6以上25以下のアリール基を表す。Ph1、Ph2はフェニル基を表す。X1は炭素数6以上25以下のアリーレン基を表す。)
An anthracene derivative represented by the general formula (2).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. R 5 represents an aryl group having 6 to 25 carbon atoms, Ph 1 and Ph 2 represent a phenyl group, and X 1 represents an arylene group having 6 to 25 carbon atoms.
一般式(3)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。X1は炭素数6以上25以下のアリーレン基を表す。)
An anthracene derivative represented by the general formula (3).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. (Ph 1 , Ph 2 , Ph 3 each represents a phenyl group, and X 1 represents an arylene group having 6 to 25 carbon atoms.)
一般式(4)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2はフェニル基を表す。X1は炭素数6以上25以下のアリーレン基を表す。)
An anthracene derivative represented by the general formula (4).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. (Ph 1 and Ph 2 each represent a phenyl group, and X 1 represents an arylene group having 6 to 25 carbon atoms.)
一般式(5)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。 5 は炭素数6以上25以下のアリール基を表す。Ph1、Ph2はフェニル基を表す。)
An anthracene derivative represented by the general formula (5).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. R 5 represents an aryl group having 6 to 25 carbon atoms , Ph 1 and Ph 2 represent a phenyl group.
一般式(6)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。 5 は炭素数6以上25以下のアリール基を表す。Ph1、Ph2はフェニル基を表す。)
An anthracene derivative represented by the general formula (6).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. R 5 represents an aryl group having 6 to 25 carbon atoms , Ph 1 and Ph 2 represent a phenyl group.
一般式(7)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR1、R2は水素または炭素数1以上4以下のアルキル基を表す。R3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。 5 は炭素数6以上25以下のアリール基を表す。Ph1、Ph2はフェニル基を表す。)
An anthracene derivative represented by the general formula (7).
Figure 2007091721
(In the formula, R 1 and R 2 represent hydrogen or an alkyl group having 1 to 4 carbon atoms. R 3 represents hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. R 5 represents an aryl group having 6 to 25 carbon atoms , Ph 1 and Ph 2 represent a phenyl group.
一般式(8)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。)
An anthracene derivative represented by the general formula (8).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 , Ph 2 , and Ph 3 represent a phenyl group.)
一般式(9)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2はフェニル基を表す。)
An anthracene derivative represented by the general formula (9).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 and Ph 2 represent a phenyl group.)
一般式(10)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。)
An anthracene derivative represented by the general formula (10).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 , Ph 2 , and Ph 3 represent a phenyl group.)
一般式(11)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2はフェニル基を表す。)
An anthracene derivative represented by the general formula (11).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 and Ph 2 represent a phenyl group.)
一般式(12)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。)
An anthracene derivative represented by the general formula (12).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 , Ph 2 , and Ph 3 represent a phenyl group.)
一般式(13)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2はフェニル基を表す。)
An anthracene derivative represented by the general formula (13).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 and Ph 2 represent a phenyl group.)
一般式(14)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。)
An anthracene derivative represented by the general formula (14).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 , Ph 2 , and Ph 3 represent a phenyl group.)
一般式(15)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。)
An anthracene derivative represented by the general formula (15).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 , Ph 2 , and Ph 3 represent a phenyl group.)
一般式(16)で表されるアントラセン誘導体。
Figure 2007091721
(式中のR3は水素、炭素数1以上4以下のアルキル基、または炭素数6以上25以下のアリール基のいずれかを表す。Ph1、Ph2、Ph3はフェニル基を表す。)
An anthracene derivative represented by the general formula (16).
Figure 2007091721
(In the formula, R 3 represents any one of hydrogen, an alkyl group having 1 to 4 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Ph 1 , Ph 2 , and Ph 3 represent a phenyl group.)
請求項1乃至請求項16のいずれか一に記載のアントラセン誘導体を含む層を、一対の電極間に有する発光素子。   A light-emitting element having a layer containing the anthracene derivative according to any one of claims 1 to 16 between a pair of electrodes. 請求項1乃至請求項16のいずれか一に記載のアントラセン誘導体と、ホストとを含む層を、一対の電極間に有し、
前記ホストは前記アントラセン誘導体のエネルギーギャップよりも大きいエネルギーギャップを有し、また前記アントラセン誘導体の有するイオン化ポテンシャルよりも大きいイオン化ポテンシャルを有する物質であることを特徴とする発光素子。
A layer containing the anthracene derivative according to any one of claims 1 to 16 and a host is provided between a pair of electrodes,
The light-emitting element, wherein the host is a substance having an energy gap larger than that of the anthracene derivative and having an ionization potential larger than that of the anthracene derivative.
請求項1乃至請求項16のいずれか一に記載のアントラセン誘導体と、発光物質とを含む層を、一対の電極間に有し、
前記発光物質は前記アントラセン誘導体のエネルギーギャップよりも小さなエネルギーギャップを有し、また前記アントラセン誘導体の有するイオン化ポテンシャルよりも小さいイオン化ポテンシャルを有する物質であることを特徴とする発光素子。
A layer containing the anthracene derivative according to any one of claims 1 to 16 and a light-emitting substance is provided between a pair of electrodes,
The light-emitting element is characterized in that the light-emitting substance has an energy gap smaller than that of the anthracene derivative and has an ionization potential smaller than that of the anthracene derivative.
請求項17乃至請求項19のいずれか一に記載の発光素子を有する発光装置。   A light emitting device comprising the light emitting element according to any one of claims 17 to 19. 請求項17乃至請求項19のいずれか一に記載の発光素子を有する電子機器。





An electronic device having the light emitting element according to any one of claims 17 to 19.





JP2006231489A 2005-09-02 2006-08-29 Anthracene derivative, light-emitting element using the anthracene derivative, light-emitting device, and electronic device Expired - Fee Related JP5041766B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2006231489A JP5041766B2 (en) 2005-09-02 2006-08-29 Anthracene derivative, light-emitting element using the anthracene derivative, light-emitting device, and electronic device

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2005254363 2005-09-02
JP2005254363 2005-09-02
JP2006231489A JP5041766B2 (en) 2005-09-02 2006-08-29 Anthracene derivative, light-emitting element using the anthracene derivative, light-emitting device, and electronic device

Publications (3)

Publication Number Publication Date
JP2007091721A JP2007091721A (en) 2007-04-12
JP2007091721A5 true JP2007091721A5 (en) 2009-10-08
JP5041766B2 JP5041766B2 (en) 2012-10-03

Family

ID=37977831

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006231489A Expired - Fee Related JP5041766B2 (en) 2005-09-02 2006-08-29 Anthracene derivative, light-emitting element using the anthracene derivative, light-emitting device, and electronic device

Country Status (1)

Country Link
JP (1) JP5041766B2 (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101579918B1 (en) 2007-04-25 2015-12-24 가부시키가이샤 한도오따이 에네루기 켄큐쇼 Organic compound anthracene derivative and light emitting element light emitting device and electronic appliance using anthracene derivative
WO2009116605A1 (en) * 2008-03-18 2009-09-24 Semiconductor Energy Laboratory Co., Ltd. Light-emitting element, light-emitting device and electronic device
WO2009116547A1 (en) 2008-03-18 2009-09-24 Semiconductor Energy Laboratory Co., Ltd. Light-emitting element, light-emitting device and electronic device
CN101752514B (en) * 2008-12-17 2015-11-25 株式会社半导体能源研究所 Light-emitting component, lighting device, light-emitting device and electronic equipment
EP2200407B1 (en) * 2008-12-17 2017-11-22 Semiconductor Energy Laboratory Co., Ltd. Light-Emitting element, light emitting device, and electronic device
US20100156957A1 (en) * 2008-12-19 2010-06-24 Semiconductor Energy Laboratory Co., Ltd. Organic compound, anthracene derivative, and light-emitting elements, light-emitting devices, electronic devices, and lighting devices using the anthracene derivative
CN102484923B (en) 2009-09-04 2016-05-04 株式会社半导体能源研究所 Light-emitting component, light-emitting device and manufacture method thereof
KR102021273B1 (en) * 2011-05-27 2019-09-16 가부시키가이샤 한도오따이 에네루기 켄큐쇼 Carbazole compound, light-emitting element, light-emitting device, electronic device, and lighting device
JP7325731B2 (en) 2018-08-23 2023-08-15 国立大学法人九州大学 organic electroluminescence element
JP7129392B2 (en) * 2018-10-26 2022-09-01 キヤノン株式会社 COMPOSITION, ORGANIC LIGHT-EMITTING DEVICE, DISPLAY DEVICE, IMAGING DEVICE, ELECTRONIC DEVICE AND MOBILE BODY HAVING THE SAME

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3511825B2 (en) * 1996-01-29 2004-03-29 東洋インキ製造株式会社 Light emitting material for organic electroluminescent device and organic electroluminescent device using the same
JP4407102B2 (en) * 2001-08-06 2010-02-03 三菱化学株式会社 Anthracene compound, method for producing the same, and organic electroluminescent device
KR100478520B1 (en) * 2001-08-13 2005-03-28 삼성에스디아이 주식회사 Blue light-emitting compound and display device adopting light-emitting compound as color-developing substance
US20030215667A1 (en) * 2001-11-02 2003-11-20 Shuang Xie Electroluminescent devices
JP4221973B2 (en) * 2002-08-28 2009-02-12 富士ゼロックス株式会社 Organic electroluminescence device
JP4122901B2 (en) * 2002-08-28 2008-07-23 富士ゼロックス株式会社 Organic electroluminescence device
KR100624407B1 (en) * 2003-01-02 2006-09-18 삼성에스디아이 주식회사 Diphenyl anthracene derivatives and organoelectroluminescent device employing the same
US7651787B2 (en) * 2003-02-19 2010-01-26 Lg Display Co., Ltd. Organic electroluminescent device
US7541097B2 (en) * 2003-02-19 2009-06-02 Lg Display Co., Ltd. Organic electroluminescent device and method for fabricating the same
JP4392206B2 (en) * 2003-07-30 2009-12-24 三井化学株式会社 Anthracene compound and organic electroluminescent device containing the anthracene compound
JP4846982B2 (en) * 2004-01-26 2011-12-28 三井化学株式会社 Anthracene compound and organic electroluminescent device containing the anthracene compound

Similar Documents

Publication Publication Date Title
JP2007091721A5 (en)
JP2008260765A5 (en)
JP2007039431A5 (en) Substance, material for light emitting element, light emitting element, light emitting device and electronic device
JP2009076835A5 (en)
JP2008137994A5 (en)
JP2010077124A5 (en) Triazole derivative and light emitting device
JP2009076834A5 (en)
JP2008162910A5 (en)
JP2006124373A5 (en)
JP2008308490A5 (en) Triazole derivative, light emitting element, light emitting device, lighting device, and electronic device
JP2010517318A5 (en)
JP2009260308A5 (en)
JP2012131775A5 (en) Carbazole compound, light emitting device, light emitting device, electronic device and lighting device
JP2010241801A5 (en)
JP2010141309A5 (en) Light emitting element
JP2008106051A5 (en)
JP2012107004A5 (en)
JP2009280576A5 (en)
JP2006298895A5 (en)
JP2008013474A5 (en) Organic compound and light emitting device
JP2008137978A5 (en)
JP2009013167A5 (en) Organometallic complex, light emitting material, light emitting element, and light emitting device
JP2007291061A5 (en)
JP2009167173A5 (en) LIGHT EMITTING ELEMENT, LIGHT EMITTING DEVICE, AND LIGHTING DEVICE
JP2013067587A5 (en) Carbazole compound, light emitting device and light emitting device