[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Zhao et al., 2011 - Google Patents

Construction of efficient solid emitters with conventional and AIE luminogens for blue organic light-emitting diodes

Zhao et al., 2011

Document ID
2037360529202606449
Author
Zhao Z
Chen S
Deng C
Lam J
Chan C
Lu P
Wang Z
Hu B
Chen X
Kwok H
Ma Y
Qiu H
Tang B
Publication year
Publication venue
Journal of Materials Chemistry

External Links

Snippet

9, 9-Bis (9-heptyl-3-carbazolyl) fluorenes (BPyBCF, BAnBCF, BTPABCF, and BTPEBCF, where B= Bis, Py= pyrene, C= carbazole, F= fluorene, An= anthracene, TPA= triphenylamine, and TPE= tetraphenylethene) with different chromophoric units at the 2, 7 …
Continue reading at pubs.rsc.org (other versions)

Classifications

    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1044Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0084Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • H01L51/0085Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077Coordination compounds, e.g. porphyrin
    • H01L51/0079Metal complexes comprising a IIIB-metal (B, Al, Ga, In or TI), e.g. Tris (8-hydroxyquinoline) gallium (Gaq3)
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0059Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1003Carbocyclic compounds
    • C09K2211/1007Non-condensed systems
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/0032Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0052Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof
    • H01L51/50Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes [OLED] or polymer light emitting devices [PLED];
    • H01L51/5012Electroluminescent [EL] layer
    • H01L51/5016Triplet emission
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L2251/00Indexing scheme relating to organic semiconductor devices covered by group H01L51/00

Similar Documents

Publication Publication Date Title
Yuan et al. Changing the behavior of chromophores from aggregation‐caused quenching to aggregation‐induced emission: development of highly efficient light emitters in the solid state
Zhao et al. Construction of efficient solid emitters with conventional and AIE luminogens for blue organic light-emitting diodes
Huang et al. Construction of efficient blue AIE emitters with triphenylamine and TPE moieties for non-doped OLEDs
Kim et al. Exceedingly efficient deep-blue electroluminescence from new anthracenes obtained using rational molecular design
Zhao et al. Using tetraphenylethene and carbazole to create efficient luminophores with aggregation-induced emission, high thermal stability, and good hole-transporting property
Chen et al. Versatile, Benzimidazole/Amine‐Based Ambipolar Compounds for Electroluminescent Applications: Single‐Layer, Blue, Fluorescent OLEDs, Hosts for Single‐Layer, Phosphorescent OLEDs
JP5813707B2 (en) Compounds for organic electronic devices
TWI611003B (en) Compounds for electronic devices
TWI762451B (en) Compounds for electronic devices
KR101884496B1 (en) Compounds for electronic devices
JP6896422B2 (en) Compounds and organic electronic devices
JP5653902B2 (en) Fluorine derivatives for organic electroluminescent devices
KR101807925B1 (en) Compounds and organic electroluminescent devices
Yu et al. Starburst 4, 4′, 4′′-tris (carbazol-9-yl)-triphenylamine-based deep-blue fluorescent emitters with tunable oligophenyl length for solution-processed undoped organic light-emitting diodes
KR20190053948A (en) Carbazoles having a diazadibenzofuran or diazadibenzothiophene structure
KR20150103241A (en) Materials for electronic devices
KR20150038193A (en) Derivatives of 2-diarylaminofluorene and organic electronic compounds containing them
KR20150036654A (en) Fluorenes and electronic devices containing them
JP2015212261A (en) Novel materials for organic electroluminescence devices
KR101979466B1 (en) Compounds for electronic devices
Ye et al. Phenyl-substituted fluorene-dimer cored anthracene derivatives: highly fluorescent and stable materials for high performance organic blue-and white-light-emitting diodes
Zhang et al. Dipolar 1, 3, 6, 8-tetrasubstituted pyrene-based blue emitters containing electro-transporting benzimidazole moieties: syntheses, structures, optical properties, electrochemistry and electroluminescence
Ye et al. Pyridine linked fluorene hybrid bipolar host for blue, green, and orange phosphorescent organic light-emitting diodes toward solution processing
Ahn et al. Electroluminescence characteristics of a new green-emitting phenylphenothiazine derivative with phenylbenzimidazole substituent
Huang et al. Blue AIE luminogens bearing methyl groups: different linkage position, different number of methyl groups, and different intramolecular conjugation