JP2005247976A5 - - Google Patents

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Publication number
JP2005247976A5
JP2005247976A5 JP2004059280A JP2004059280A JP2005247976A5 JP 2005247976 A5 JP2005247976 A5 JP 2005247976A5 JP 2004059280 A JP2004059280 A JP 2004059280A JP 2004059280 A JP2004059280 A JP 2004059280A JP 2005247976 A5 JP2005247976 A5 JP 2005247976A5
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JP
Japan
Prior art keywords
group
transistors
tert
display panel
driver circuit
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JP2004059280A
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Japanese (ja)
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JP2005247976A (en
JP4521207B2 (en
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Priority claimed from JP2004059280A external-priority patent/JP4521207B2/en
Priority to JP2004059280A priority Critical patent/JP4521207B2/en
Priority to PCT/JP2004/009660 priority patent/WO2005005408A1/en
Priority to US10/564,039 priority patent/US7521567B2/en
Priority to KR1020067000745A priority patent/KR20060041223A/en
Priority to TW093120697A priority patent/TW200512272A/en
Publication of JP2005247976A publication Critical patent/JP2005247976A/en
Publication of JP2005247976A5 publication Critical patent/JP2005247976A5/ja
Publication of JP4521207B2 publication Critical patent/JP4521207B2/en
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Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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一般式1において、R乃至Rは、それぞれ独立に、水素原子又は置換基を表す。R乃至Rにおける置換基としては、例えば、メチル基、エチル基、プロピル基、イソプロピル基、イソプロペニル基、1−プロペニル基、1−プロピニル基、2−プロペニル基、ブチル基、イソブチル基、sec−ブチル基、tert−ブチル基、2−ブテニル、1,3−ブタジエニル基、ペンチル基、イソペンチル基、ネオペンチル基、tert−ペンチル基、1−メチルペンチル基、2−メチルペンチル基、2−ペンテニル基、2−ペンテン−4−イニル基、ヘキシル基、イソヘキシル基、5−メチルヘキシル基、ヘプチル基、オクチル基、ノニル基、デシル基、ドデシル基などの脂肪族炭化水素基、シクロプロピル基、シクロブチル基、シクロペンチル基、シクロペンテニル基、シクロペンタジエニル基、シクロヘキシル基、シクロヘキセニル基、シクロヘキサジエニル基、シクロヘプチル基、シクロオクチル基、シクロオクタジエニル基などの脂環式炭化水素基、フェニル基、o−トリル基、m−トリル基、p−トリル基、キシリル基、メシチル基、o−クメニル基、m−クメニル基、p−クメニル基、ビフェニリル基、ナフチル基、アントリル基、フェナレニル基、フェナントリル基、ピレニル基などの芳香族炭化水素基、メトキシ基、エトキシ基、プロポキシ基、イソプロポキシ基、ブトキシ基、イソブトキシ基、sec−ブトキシ基、tert−ブトキシ基、ペンチルオキシ基、イソペンチルオキシ基、ヘキシルオキシ基、アリルオキシ基、フェノキシ基、ナフチルオキシ基などのエーテル基、メトキシカルボニル基、エトキシカルボニル基、プロポキシカルボニル基、アセトキシ基、ベンゾイルオキシ基などのエステル基、メチルアミノ基、ジメチルアミノ基、エチルアミノ基、ジエチルアミノ基、プロピルアミノ基、ジプロピルアミノ基、イソプロピルアミノ基、ジイソプロピルアミノ基、ブチルアミノ基、ジブチルアミノ基、イソブチルアミノ基、ジイソブチルアミノ基、sec−ブチルアミノ基、tert−ブチルアミノ基、ペンチルアミノ基、ジペンチルアミノ基、ヘキシルアミノ基、シクロヘキシルアミノ基、ピペリジノ基、フェニルアミノ基、N,N−ジフェニルアミノ基、ナフチルアミノ基、N,N−ナフチルフェニルアミノ基、N,N−ジナフチルアミノ基、N−カルバゾリル基などのアミノ基、フルオロ基、クロロ基、ブロモ基、ヨード基などのハロゲン基、ヒドロキシ基、カルボキシ基、シアノ基、ニトロ基、さらには、それらの組合わせによる置換基が挙げられる。 In General Formula 1, R 1 to R 5 each independently represents a hydrogen atom or a substituent. Examples of the substituent in R 1 to R 5 include a methyl group, an ethyl group, a propyl group, an isopropyl group, an isopropenyl group, a 1-propenyl group, a 1-propynyl group, a 2-propenyl group, a butyl group, an isobutyl group, sec-butyl group, tert-butyl group, 2-butenyl group , 1,3-butadienyl group, pentyl group, isopentyl group, neopentyl group, tert-pentyl group, 1-methylpentyl group, 2-methylpentyl group, 2- Pentenyl group, 2-pentene-4-ynyl group, hexyl group, isohexyl group, 5-methylhexyl group, heptyl group, octyl group, nonyl group, decyl group, dodecyl group and other aliphatic hydrocarbon groups, cyclopropyl group, Cyclobutyl group, cyclopentyl group, cyclopentenyl group, cyclopentadienyl group, cyclohexyl group, Cyclohexenyl group, cyclohexadienyl group, cycloheptyl group, cyclooctyl group, cyclooctadienyl group and other alicyclic hydrocarbon groups, phenyl group, o-tolyl group, m-tolyl group, p-tolyl group, xylyl Group, mesityl group, o-cumenyl group, m-cumenyl group, p-cumenyl group, biphenylyl group, naphthyl group, anthryl group, phenalenyl group, phenanthryl group, pyrenyl group and other aromatic hydrocarbon groups, methoxy group, ethoxy group , Ether groups such as propoxy group, isopropoxy group, butoxy group, isobutoxy group, sec-butoxy group, tert-butoxy group, pentyloxy group, isopentyloxy group, hexyloxy group, allyloxy group, phenoxy group, naphthyloxy group , Methoxycarbonyl group, ethoxycarbonyl group, propoxycal Ester group such as bonyl group, acetoxy group, benzoyloxy group, methylamino group, dimethylamino group, ethylamino group, diethylamino group, propylamino group, dipropylamino group, isopropylamino group, diisopropylamino group, butylamino group, Dibutylamino group, isobutylamino group, diisobutylamino group, sec-butylamino group, tert-butylamino group, pentylamino group, dipentylamino group, hexylamino group, cyclohexylamino group, piperidino group, phenylamino group, N, N -Halogens such as amino groups such as diphenylamino group, naphthylamino group, N, N-naphthylphenylamino group, N, N-dinaphthylamino group and N-carbazolyl group, fluoro group, chloro group, bromo group and iodo group Group, hydroxy group, Bokishi group, a cyano group, a nitro group, further include a substituent by combination thereof.

48はこの発明の有機EL素子を主体とする表示パネルであり、ドライバ回路36、46を介してマイクロコンピューター38へ接続されている。ドライバ回路36は、昇圧回路からの直流電圧が表示パネル48へ印加されるのを制御する回路であって、表示パネル48における垂直方向の電極列へ個別に接続される複数のトランジスタを含んでなる。したがって、このドライバ回路36におけるトランジスタのいずれかがオンすると、そのトランジスタへ接続されている垂直方向の電極列へ昇圧回路32からの電圧が印加されることとなる。一方、ドライバ回路46は、表示パネル48の水平方向の電極列へ個別に接続される複数のトランジスタを含んでなり、ドライバ回路46におけるトランジスタのいずれかがオンすると、そのトランジスタへ接続されている水平方向の電極列が接地されることとなる。 A display panel 48 mainly composed of the organic EL element of the present invention is connected to the microcomputer 38 via driver circuits 36 and 46. The driver circuit 36 is a circuit that controls application of a DC voltage from the booster circuit to the display panel 48, and includes a plurality of transistors individually connected to the vertical electrode rows in the display panel 48. . Therefore, when any of the transistors in the driver circuit 36 is turned on, the voltage from the booster circuit 32 is applied to the vertical electrode row connected to the transistor. On the other hand, the driver circuit 46 includes a plurality of transistors individually connected to the horizontal electrode rows of the display panel 48, and when any of the transistors in the driver circuit 46 is turned on, the horizontal connection connected to the transistors is made. The electrode array in the direction is grounded.

JP2004059280A 2003-07-11 2004-03-03 Organic electroluminescence device Expired - Fee Related JP4521207B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP2004059280A JP4521207B2 (en) 2004-03-03 2004-03-03 Organic electroluminescence device
PCT/JP2004/009660 WO2005005408A1 (en) 2003-07-11 2004-07-07 Amine compound and uses thereof
US10/564,039 US7521567B2 (en) 2003-07-11 2004-07-07 Amine compound and uses thereof
KR1020067000745A KR20060041223A (en) 2003-07-11 2004-07-07 Amine compound and uses thereof
TW093120697A TW200512272A (en) 2003-07-11 2004-07-09 Amine compounds and use thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004059280A JP4521207B2 (en) 2004-03-03 2004-03-03 Organic electroluminescence device

Publications (3)

Publication Number Publication Date
JP2005247976A JP2005247976A (en) 2005-09-15
JP2005247976A5 true JP2005247976A5 (en) 2007-04-05
JP4521207B2 JP4521207B2 (en) 2010-08-11

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JP2004059280A Expired - Fee Related JP4521207B2 (en) 2003-07-11 2004-03-03 Organic electroluminescence device

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JP (1) JP4521207B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4843321B2 (en) * 2006-01-31 2011-12-21 Jnc株式会社 Coumarin compound, material for light emitting device, and organic electroluminescent device
TW201026344A (en) 2008-10-08 2010-07-16 Hayashibara Biochem Lab Lighting device

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5788455A (en) * 1980-11-22 1982-06-02 Canon Inc Electrophotographic receptor
JP3215718B2 (en) * 1992-06-19 2001-10-09 株式会社日本化学工業所 Fluorescent detector
JPH06122874A (en) * 1992-08-25 1994-05-06 Konica Corp Organic electroluminescent element

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