Zhao et al., 2011 - Google Patents
Construction of efficient solid emitters with conventional and AIE luminogens for blue organic light-emitting diodesZhao 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 …
- 239000007787 solid 0 title abstract description 15
Classifications
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
- H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
- H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- 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
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H01L51/0085—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising Iridium
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/0077—Coordination compounds, e.g. porphyrin
- H01L51/0079—Metal complexes comprising a IIIB-metal (B, Al, Ga, In or TI), e.g. Tris (8-hydroxyquinoline) gallium (Gaq3)
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0059—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
- H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
- H01L51/0052—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
-
- H—ELECTRICITY
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L51/00—Solid 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
- H01L51/50—Solid 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];
- H01L51/5012—Electroluminescent [EL] layer
- H01L51/5016—Triplet emission
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
- 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
- H01—BASIC ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H01L2251/00—Indexing 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 |