JP2007070352A5 - - Google Patents

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JP2007070352A5
JP2007070352A5 JP2006217779A JP2006217779A JP2007070352A5 JP 2007070352 A5 JP2007070352 A5 JP 2007070352A5 JP 2006217779 A JP2006217779 A JP 2006217779A JP 2006217779 A JP2006217779 A JP 2006217779A JP 2007070352 A5 JP2007070352 A5 JP 2007070352A5
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carbon atoms
group
light emitting
light
general formula
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Claims (13)

一般式（１）で表される第２級アリールアミン化合物。
Figure 2007070352
 （式中、Ａｒ11は炭素数７〜２５のアリール基、炭素数７〜２５のヘテロアリール基のいずれかを表し、Ａｒ12およびＡｒ13はそれぞれ同一でも異なっていても良く、炭素数６〜９のアリール基、炭素数５〜９のヘテロアリール基のいずれかを表し、Ｘは炭素数６〜２５の２価の芳香族炭化水素基、炭素数５〜１０の２価の複素環基のいずれかを表す。） A secondary arylamine compound represented by the general formula (1).
Figure 2007070352
 (In the formula, Ar 11 represents either an aryl group having 7 to 25 carbon atoms or a heteroaryl group having 7 to 25 carbon atoms, and Ar 12 and Ar 13 may be the same or different, and 9 represents an aryl group having 5 or 9 to 9 carbon atoms, and X represents a divalent aromatic hydrocarbon group having 6 to 25 carbon atoms or a divalent heterocyclic group having 5 to 10 carbon atoms. Represents either one.) 一般式（２）で表される第２級アリールアミン化合物。
Figure 2007070352
 （式中、Ａｒ22およびＡｒ23はそれぞれ同一でも異なっていても良く、炭素数６〜９のアリール基、炭素数５〜９のヘテロアリール基のいずれかを表し、Ｘは炭素数６〜２５の２価の芳香族炭化水素基、炭素数５〜１０の２価の複素環基のいずれかを表す。） A secondary arylamine compound represented by the general formula (2).
Figure 2007070352
 (In the formula, Ar 22 and Ar 23 may be the same or different and each represents an aryl group having 6 to 9 carbon atoms or a heteroaryl group having 5 to 9 carbon atoms, and X is 6 to 25 carbon atoms. Or a divalent heterocyclic group having 5 to 10 carbon atoms.) 構造式（３１）で表される第２級アリールアミン化合物。
Figure 2007070352
 A secondary arylamine compound represented by Structural Formula (31).
Figure 2007070352
 請求項１乃至請求項３のいずれか一項に記載の第２級アリールアミンのアミンに結合した水素を置換して合成した第３級アリールアミン構造を有する化合物。 The compound which has the tertiary arylamine structure synthesize | combined by substituting the hydrogen couple | bonded with the amine of the secondary arylamine as described in any one of Claims 1 thru | or 3. 一般式（４）で示される化合物。
Figure 2007070352
 （式中、Ａｒ11は炭素数７〜２５のアリール基、炭素数７〜２５のヘテロアリール基のいずれかを表し、Ａｒ12およびＡｒ13はそれぞれ同一でも異なっていても良く、炭素数６〜９のアリール基、炭素数５〜９のヘテロアリール基のいずれかを表し、Ｘは炭素数６〜２５の２価の芳香族炭化水素基、炭素数５〜１０の２価の複素環基のいずれかを表し、Ｒ1は、水素、炭素数１〜６のアルキル基、炭素数６〜２５のアリール基、炭素数５〜９のヘテロアリール基、アリールアルキル基、炭素数１〜７のアシル基のいずれかを表し、Ｒ2は、水素、炭素数１〜６のアルキル基、一般式（５）で示される置換基のいずれかを表す。
Figure 2007070352
 一般式（５）中、Ａｒ14は炭素数７〜２５のアリール基、炭素数７〜２５のヘテロアリール基のいずれかを表し、Ａｒ15およびＡｒ16はそれぞれ同一でも異なっていても良く、炭素数６〜９のアリール基、炭素数５〜９のヘテロアリール基のいずれかを表し、Ｙは炭素数６〜２５の２価の芳香族炭化水素基、炭素数５〜１０の２価の複素環基のいずれかを表す。） A compound represented by the general formula (4).
Figure 2007070352
 (In the formula, Ar 11 represents either an aryl group having 7 to 25 carbon atoms or a heteroaryl group having 7 to 25 carbon atoms, and Ar 12 and Ar 13 may be the same or different, and 9 represents an aryl group having 5 or 9 to 9 carbon atoms, and X represents a divalent aromatic hydrocarbon group having 6 to 25 carbon atoms or a divalent heterocyclic group having 5 to 10 carbon atoms. R 1 represents any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 25 carbon atoms, a heteroaryl group having 5 to 9 carbon atoms, an arylalkyl group, and an acyl having 1 to 7 carbon atoms. R 2 represents any one of a group represented by hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituent represented by the general formula (5).
Figure 2007070352
 In the general formula (5), Ar 14 represents either an aryl group having 7 to 25 carbon atoms or a heteroaryl group having 7 to 25 carbon atoms, and Ar 15 and Ar 16 may be the same or different, and Any one of an aryl group having 6 to 9 carbon atoms and a heteroaryl group having 5 to 9 carbon atoms, Y is a divalent aromatic hydrocarbon group having 6 to 25 carbon atoms, and a divalent complex having 5 to 10 carbon atoms Represents any of the cyclic groups. ) 一般式（６）で示される化合物。
Figure 2007070352
 （式中、Ａｒ22およびＡｒ23はそれぞれ同一でも異なっていても良く、炭素数６〜９のアリール基、炭素数５〜９のヘテロアリール基のいずれかを表し、Ｘは炭素数６〜２５の２価の芳香族炭化水素基、炭素数５〜１０の２価の複素環基のいずれかを表し、Ｒ1は、水素、炭素数１〜６のアルキル基、炭素数６〜２５のアリール基、炭素数５〜９のヘテロアリール基、アリールアルキル基、炭素数１〜７のアシル基のいずれかを表し、Ｒ2は、水素、炭素数１〜６のアルキル基、一般式（７）で示される置換基のいずれかを表す。
Figure 2007070352
 一般式（７）中、Ａｒ25およびＡｒ26はそれぞれ同一でも異なっていても良く、炭素数６〜９のアリール基、炭素数５〜９のヘテロアリール基のいずれかを表し、Ｙは炭素数６〜２５の２価の芳香族炭化水素基、炭素数５〜１０の２価の複素環基のいずれかを表す。） Compound represented by the general formula (6).
Figure 2007070352
 (In the formula, Ar 22 and Ar 23 may be the same or different and each represents an aryl group having 6 to 9 carbon atoms or a heteroaryl group having 5 to 9 carbon atoms, and X is 6 to 25 carbon atoms. Represents a divalent aromatic hydrocarbon group or a divalent heterocyclic group having 5 to 10 carbon atoms, and R 1 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, or an aryl group having 6 to 25 carbon atoms. Group, a heteroaryl group having 5 to 9 carbon atoms, an arylalkyl group, or an acyl group having 1 to 7 carbon atoms, R 2 is hydrogen, an alkyl group having 1 to 6 carbon atoms, or a general formula (7) Any one of the substituents represented by
Figure 2007070352
 In general formula (7), Ar 25 and Ar 26 may be the same or different and each represents an aryl group having 6 to 9 carbon atoms or a heteroaryl group having 5 to 9 carbon atoms, and Y represents the number of carbon atoms It represents either a 6-25 divalent aromatic hydrocarbon group or a divalent heterocyclic group having 5-10 carbon atoms. ) 一般式（８）で表される化合物。
Figure 2007070352
 （式中、Ｒ1は、水素、炭素数１〜６のアルキル基、炭素数６〜２５のアリール基、炭素数５〜９のヘテロアリール基、アリールアルキル基、炭素数１〜７のアシル基のいずれかを表し、Ｒ2は、水素、炭素数１〜６のアルキル基、構造式（９）で示される置換基のいずれかを表す。）
Figure 2007070352
 The compound represented by General formula (8).
Figure 2007070352
 (In the formula, R 1 is hydrogen, an alkyl group having 1 to 6 carbon atoms, an aryl group having 6 to 25 carbon atoms, a heteroaryl group having 5 to 9 carbon atoms, an arylalkyl group, or an acyl group having 1 to 7 carbon atoms. R 2 represents any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituent represented by the structural formula (9).)
Figure 2007070352
 一対の電極間に発光物質を含む層を有し、前記発光物質を含む層は、請求項４乃至請求項７のいずれか一項に記載の化合物を含むことを特徴とする発光素子。 A layer containing a light emitting substance between a pair of electrodes, the layer containing the light emitting substance includes a light emitting device characterized by comprising a compound according to any one of claims 4 to 7. 第１の電極と、第２の電極との間に、発光物質を含む層を有し、前記発光物質を含む層は、発光層を有し、前記発光層よりも第１の電極側に、請求項４乃至請求項７のいずれか一項に記載の化合物を含む層を有し、前記第１の電極の電位の方が前記第２極の電位よりも高くなるように電圧を印加したときに前記発光物質が発光することを特徴とする発光素子。 Between the 1st electrode and the 2nd electrode, it has a layer containing a luminescent substance, the layer containing the luminescent substance has a luminescent layer, and the 1st electrode side rather than the luminescent layer, a layer comprising a compound according to any one of claims 4 to 7, when the person of the potential of the first electrode is applied a voltage to be higher than the potential of the second pole A light-emitting element, wherein the light-emitting substance emits light. 一対の電極間に発光物質を含む層を有し、前記発光物質を含む層は、発光層を有し、前記発光層は、請求項４乃至請求項７のいずれか一項に記載の化合物を含むことを特徴とする発光素子。 A layer containing a light-emitting substance is provided between a pair of electrodes, the layer containing the light-emitting substance has a light-emitting layer, and the light-emitting layer contains the compound according to any one of claims 4 to 7. A light emitting element including the light emitting element. 一対の電極間に発光物質を含む層を有し、前記発光物質は、請求項４乃至請求項７のいずれか一項に記載の化合物であることを特徴とする発光素子。 A layer containing a light emitting substance between a pair of electrodes, said luminescent material emitting element which is a compound according to any one of claims 4 to 7. 請求項８乃至請求項１１のいずれか一項に記載の発光素子と、前記発光素子の発光を制御する制御手段とを有する発光装置。 A light emitting device comprising: the light emitting element according to any one of claims 8 to 11; and a control unit that controls light emission of the light emitting element. 表示部を有し、前記表示部は、請求項８乃至請求項１１のいずれか一項に記載の発光素子と前記発光素子の発光を制御する制御手段とを備えたことを特徴とする電子機器。   An electronic apparatus comprising: a display unit, wherein the display unit includes the light emitting element according to any one of claims 8 to 11 and a control unit that controls light emission of the light emitting element. .
JP2006217779A 2005-08-12 2006-08-10 Arylamine compound and its synthesis method, and light emitting element material, light emitting element and electronic device obtained by using the arylamine compound Withdrawn JP2007070352A (en)

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JP2567075B2 (en) * 1988-12-16 1996-12-25 三井東圧化学株式会社 Dichroic dye for liquid crystal display
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US6602619B2 (en) * 2001-10-19 2003-08-05 Lightronik Technology Inc. Organic EL device
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JP4135411B2 (en) * 2002-06-26 2008-08-20 三菱化学株式会社 Asymmetric 1,4-phenylenediamine derivative and organic electroluminescence device using the same
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US7300709B2 (en) * 2004-03-31 2007-11-27 Eastman Kodak Company Organic element for electroluminescent devices
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