JP5808252B2 - カルバゾール、ジベンゾフラン、ジベンゾチオフェンおよびジベンゾホスホールから選択されたシリル置換およびヘテロ原子置換された化合物および該化合物の有機エレクトロニクスへの使用 - Google Patents

カルバゾール、ジベンゾフラン、ジベンゾチオフェンおよびジベンゾホスホールから選択されたシリル置換およびヘテロ原子置換された化合物および該化合物の有機エレクトロニクスへの使用 Download PDF

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JP5808252B2
JP5808252B2 JP2011544828A JP2011544828A JP5808252B2 JP 5808252 B2 JP5808252 B2 JP 5808252B2 JP 2011544828 A JP2011544828 A JP 2011544828A JP 2011544828 A JP2011544828 A JP 2011544828A JP 5808252 B2 JP5808252 B2 JP 5808252B2
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substituted
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JP2012514618A5 (cg-RX-API-DMAC7.html
JP2012514618A (ja
Inventor
ランガー ニコル
ランガー ニコル
シルトクネヒト クリスティアン
シルトクネヒト クリスティアン
惣一 渡部
惣一 渡部
フックス エヴェリン
フックス エヴェリン
ヴァーゲンブラスト ゲアハルト
ヴァーゲンブラスト ゲアハルト
レナルツ クリスティアン
レナルツ クリスティアン
モルト オリヴァー
モルト オリヴァー
ドアマン コリンナ
ドアマン コリンナ
ロー チュアンジエ
ロー チュアンジエ
アーヴィト　フンツェ
フンツェ アーヴィト
ラルフ　クラウゼ
クラウゼ ラルフ
シュミート ギュンター
シュミート ギュンター
ホイザー カルステン
ホイザー カルステン
ファン エルスベアゲン フォルカー
ファン エルスベアゲン フォルカー
フリードリヒ ベアナー ヘアバート
フリードリヒ ベアナー ヘアバート
キルシュ シュテファン
キルシュ シュテファン
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BASF SE
Philips Intellectual Property and Standards GmbH
Ams Osram International GmbH
Koninklijke Philips NV
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BASF SE
Osram Opto Semiconductors GmbH
Philips Intellectual Property and Standards GmbH
Koninklijke Philips NV
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
    • C07F9/572—Five-membered rings
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    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
    • C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
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    • C07F7/02—Silicon compounds
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
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    • C07F9/655354—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
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    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
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    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
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    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
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    • H10K2101/00—Properties of the organic materials covered by group H10K85/00
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    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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  • Organic Chemistry (AREA)
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  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Electroluminescent Light Sources (AREA)
JP2011544828A 2009-01-07 2009-12-14 カルバゾール、ジベンゾフラン、ジベンゾチオフェンおよびジベンゾホスホールから選択されたシリル置換およびヘテロ原子置換された化合物および該化合物の有機エレクトロニクスへの使用 Active JP5808252B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP09150176 2009-01-07
EP09150181 2009-01-07
EP09150176.7 2009-01-07
EP09150181.7 2009-01-07
PCT/EP2009/067120 WO2010079051A1 (de) 2009-01-07 2009-12-14 Silyl- und heteroatom-substituierte verbindungen ausgewählt aus carbazolen, dibenzofuranen, dibenzothiophenen und dibenzophospholen und ihre anwendung in der organischen elektronik

Publications (3)

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JP2012514618A JP2012514618A (ja) 2012-06-28
JP2012514618A5 JP2012514618A5 (cg-RX-API-DMAC7.html) 2015-08-27
JP5808252B2 true JP5808252B2 (ja) 2015-11-10

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US (1) US9458182B2 (cg-RX-API-DMAC7.html)
EP (1) EP2393819B9 (cg-RX-API-DMAC7.html)
JP (1) JP5808252B2 (cg-RX-API-DMAC7.html)
KR (1) KR101693903B1 (cg-RX-API-DMAC7.html)
CN (1) CN102341403B (cg-RX-API-DMAC7.html)
WO (1) WO2010079051A1 (cg-RX-API-DMAC7.html)

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