Wang et al., 2008 - Google Patents
Novel host materials for single-component white organic light-emitting diodes based on 9-naphthylanthracene derivativesWang et al., 2008
View PDF- Document ID
- 16706157901828529490
- Author
- Wang L
- Wong W
- Lin M
- Wong W
- Cheah K
- Tam H
- Chen C
- Publication year
- Publication venue
- Journal of Materials Chemistry
External Links
Snippet
A series of 9-naphthylanthracene based dimers and trimers were synthesized and characterized. TGA studies reveal that they are all thermally stable with decomposition temperatures well above 500° C. Upon optical excitation, all of these dimers and trimers …
- 239000000463 material 0 title abstract description 14
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
-
- 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
- H01L51/0077—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
- H01L51/0052—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0033—Iridium compounds
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Wang et al. | Novel host materials for single-component white organic light-emitting diodes based on 9-naphthylanthracene derivatives | |
Wan et al. | Multifunctional electron-transporting indolizine derivatives for highly efficient blue fluorescence, orange phosphorescence host and two-color based white OLEDs | |
Zhang et al. | New phosphorescent platinum (II) Schiff base complexes for PHOLED applications | |
KR100578424B1 (en) | New organic compounds for electroluminescence and organic electroluminescent devices using the same | |
Chen et al. | Synthesis, structure and luminescence properties of zinc (II) complexes with terpyridine derivatives as ligands | |
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 | |
TWI526448B (en) | Organic metal compound, and organic light-emitting device employing the same | |
JP2011037838A (en) | Benzofluorene compound, material for luminous layer and organic electroluminescent device using the compound | |
JP2007299980A (en) | Organic electroluminescence device | |
JP7193649B2 (en) | Compounds for organic light-emitting devices and long-lived organic light-emitting devices containing the same | |
Dai et al. | Iridium (III) complexes with enhanced film amorphism as guests for efficient orange solution-processed single-layer PhOLEDs with low efficiency roll-off | |
He et al. | Light-emitting dyes derived from bifunctional chromophores of diarylamine and oxadiazole: Synthesis, crystal structure, photophysics and electroluminescence | |
Wang et al. | Tuning electron injection/transporting properties of 9, 10-diphenylanthracene based electron transporters via optimizing the number of peripheral pyridine for highly efficient fluorescent OLEDs | |
Liu et al. | A new strategy to synthesize three-coordinate mononuclear copper (I) halide complexes containing a bulky terphenyl bidentate phosphine ligand and their luminescent properties | |
Giridhar et al. | A systematic identification of efficiency enrichment between thiazole and benzothiazole based yellow iridium (III) complexes | |
Huang et al. | Synthesis and characterization of highly stable and efficient star-molecules | |
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 | |
JP5007988B2 (en) | Polycyclic fused-ring compounds, production methods thereof, and organic electroluminescent devices using the polycyclic fused-ring compounds | |
Zhao et al. | 1, 3, 6, 8-Tetrakis [(triisopropylsilyl) ethynyl] pyrene: A highly efficient solid-state emitter for non-doped yellow electroluminescence devices | |
Tao et al. | A triphenylamine derivative as a single-emitting component for highly-efficient white electroluminescent devices | |
TWI390007B (en) | Triptycene derivatives and their application | |
JP5024655B2 (en) | Cross-linked stilbene derivatives and organic electroluminescent devices using them | |
WO2021000434A1 (en) | Red, green and blue thermally activated delayed fluorescent material, synthesis method therefor and use thereof | |
KR101369662B1 (en) | New Compounds, KL Host Material And Organic Light Emitting Device | |
Chen et al. | Synthesis, characterization and electroluminescence of B (III) compounds: BPh2 (2-(2-quinolyl) naphtho [b] imidazolato) and BPh2 (2-(2-quinolyl) benzimidazolato) |