TW200740823A - Oxadiazole-substituted Sym-triindole derivative and organic el element employing the same - Google Patents
Oxadiazole-substituted Sym-triindole derivative and organic el element employing the sameInfo
- Publication number
- TW200740823A TW200740823A TW095127275A TW95127275A TW200740823A TW 200740823 A TW200740823 A TW 200740823A TW 095127275 A TW095127275 A TW 095127275A TW 95127275 A TW95127275 A TW 95127275A TW 200740823 A TW200740823 A TW 200740823A
- Authority
- TW
- Taiwan
- Prior art keywords
- organic
- derivative
- oxadiazole
- same
- sym
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
- H10K85/6565—Oxadiazole compounds
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
- C09K2211/1048—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms with oxygen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1059—Heterocyclic compounds characterised by ligands containing three nitrogen atoms as heteroatoms
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- 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
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Electroluminescent Light Sources (AREA)
- Luminescent Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
An Sym-triindole derivative which has excellent film-forming properties and is bipolar. Even when used to form a single-layer organic EL element, the derivative luminesces. It is hence widely applicable to the field of organic EL materials, etc., and is especially suitable for use in an organic EL element. The derivative is an oxadiazole-substituted Sym-triindole derivative represented by the general formula (1): (1) (wherein R1 to R5 each independently represents hydrogen, fluorine, C1-12 alkyl, etc.; and R6 represents C2-12 alkyl, etc.). Also provided is a process for producing the derivative.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2005223152 | 2005-08-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
TW200740823A true TW200740823A (en) | 2007-11-01 |
Family
ID=37708694
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW095127275A TW200740823A (en) | 2005-08-01 | 2006-07-26 | Oxadiazole-substituted Sym-triindole derivative and organic el element employing the same |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPWO2007015414A1 (en) |
TW (1) | TW200740823A (en) |
WO (1) | WO2007015414A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2282742A1 (en) * | 2008-04-09 | 2011-02-16 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
US9169206B2 (en) * | 2008-12-23 | 2015-10-27 | Luminano Co., Ltd. | Organic semiconductor compound, method for preparing the same, and organic semiconductor composition, and organic semiconductor thin film and element containing the same |
CN102295647B (en) * | 2011-08-15 | 2013-07-17 | 华东师范大学 | All-alkyl substituted triindenyl cyclopi trimeric-indole derivative and preparation method thereof |
CN103304568B (en) * | 2013-06-28 | 2015-11-18 | 中国科学院宁波材料技术与工程研究所 | Trimerization Benzazole compounds and its production and use |
GB201717193D0 (en) * | 2017-10-19 | 2017-12-06 | Univ Durham | Thermally activated delayed fluorescence molecules, materials comprising said molecules, and devices comprising said materials |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0794807A (en) * | 1993-07-27 | 1995-04-07 | Toshiba Corp | Amorphous organic thin film element, amorphous organic polymer compound and amorphous inorganic compound |
JP4499846B2 (en) * | 1998-05-07 | 2010-07-07 | 富山化学工業株式会社 | Method for producing 7-isoindoline-quinolonecarboxylic acid derivative and method for producing isoindoline-5-boronic acid derivative |
JPWO2003050201A1 (en) * | 2001-12-12 | 2005-04-21 | 株式会社トクヤマ | Organic electroluminescence element material |
DE10211597A1 (en) * | 2002-03-15 | 2003-10-02 | Merck Patent Gmbh | Process for the production of ring connections |
JP2004224774A (en) * | 2003-01-27 | 2004-08-12 | Mitsubishi Rayon Co Ltd | Indole derivative trimer, method for producing the same and light-emitting element using the same |
US7632954B2 (en) * | 2004-02-16 | 2009-12-15 | Ihara Chemical Industry Co., Ltd. | Substituted sym-triindole |
-
2006
- 2006-07-26 TW TW095127275A patent/TW200740823A/en unknown
- 2006-07-27 WO PCT/JP2006/314861 patent/WO2007015414A1/en active Application Filing
- 2006-07-27 JP JP2007529227A patent/JPWO2007015414A1/en active Pending
Also Published As
Publication number | Publication date |
---|---|
WO2007015414A1 (en) | 2007-02-08 |
JPWO2007015414A1 (en) | 2009-02-19 |
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