Kreyenschmidt et al., 1998 - Google Patents
Thermally stable blue-light-emitting copolymers of poly (alkylfluorene)Kreyenschmidt et al., 1998
- Document ID
- 8029485863487531046
- Author
- Kreyenschmidt M
- Klaerner G
- Fuhrer T
- Ashenhurst J
- Karg S
- Chen W
- Lee V
- Scott J
- Miller R
- Publication year
- Publication venue
- Macromolecules
External Links
Snippet
We have prepared a variety of high molecular weight, thermally stable, blue-light-emitting random copolymers of 9, 9-di-n-hexylfluorene by nickel (0)-mediated polymerization. The copolymers are readily soluble and easily processable from organic solvents. Both the …
- 229920001577 copolymer 0 title abstract description 101
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
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
- H01L51/0038—Poly-phenylenevinylene and derivatives
-
- 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
-
- 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
-
- 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
- H01L51/0032—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
- H01L51/0069—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S comprising two or more different heteroatoms per ring, e.g. S and N
- H01L51/007—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S comprising two or more different heteroatoms per ring, e.g. S and N oxadiazole compounds
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/54—Material technologies
- Y02E10/549—Material technologies organic PV cells
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
-
- 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 |
---|---|---|
Kreyenschmidt et al. | Thermally stable blue-light-emitting copolymers of poly (alkylfluorene) | |
Marsitzky et al. | Amorphous poly-2, 7-fluorene networks | |
Klärner et al. | Cross-linkable polymers based on dialkylfluorenes | |
Lee et al. | Oxidative stability and its effect on the photoluminescence of poly (fluorene) derivatives: end group effects | |
Song et al. | Highly efficient light-emitting polymers composed of both hole and electron affinity units in the conjugated main chain | |
Kulkarni et al. | Blue light-emitting diodes with good spectral stability based on blends of poly (9, 9-dioctylfluorene): interplay between morphology, photophysics, and device performance | |
Kulkarni et al. | Quinoxaline-containing polyfluorenes: synthesis, photophysics, and stable blue electroluminescence | |
Lee et al. | Luminescence properties of structurally modified PPVs: PPV derivatives bearing 2-(4-tert-butylphenyl)-5-phenyl-1, 3, 4-oxadiazole pendants | |
Shu et al. | Highly efficient blue-light-emitting diodes from polyfluorene containing bipolar pendant groups | |
Peng et al. | Polymers with bipolar carrier transport abilities for light emitting diodes | |
Alam et al. | Polybenzobisazoles are efficient electron transport materials for improving the performance and stability of polymer light-emitting diodes | |
Kim et al. | Blue light emitting polymers | |
Lu et al. | Pure deep blue light-emitting diodes from alternating fluorene/carbazole copolymers by using suitable hole-blocking materials | |
Zeng et al. | Spectral and thermal spectral stability study for fluorene-based conjugated polymers | |
Marsitzky et al. | Self-encapsulation of poly-2, 7-fluorenes in a dendrimer matrix | |
Pei et al. | Efficient photoluminescence and electroluminescence from a soluble polyfluorene | |
Pei et al. | A novel series of efficient thiophene-based light-emitting conjugated polymers and application in polymer light-emitting diodes | |
Chou et al. | Synthesis and characterization of luminescent polyfluorenes incorporating side-chain-tethered polyhedral oligomeric silsesquioxane units | |
Li et al. | “AB2+ AB” approach to hyperbranched polymers used as polymer blue light emitting materials | |
Babel et al. | Charge carrier mobility in blends of poly (9, 9-dioctylfluorene) and poly (3-hexylthiophene) | |
Cho et al. | Synthesis and color tuning of new fluorene-based copolymers | |
Kang et al. | Highly improved quantum efficiency in blend polymer LEDs | |
Chou et al. | Synthesis and characterization of dendronized polyfluorenes | |
Alam et al. | Nanophase-Separated Blends of Acceptor and Donor Conjugated Polymers. Efficient Electroluminescence from Binary Polyquinoline/Poly (2-methoxy-5-(2 ‘-ethylhexyloxy)-1, 4-phenylenevinylene) and Polyquinoline/Poly (3-octylthiophene) Blends | |
Liu et al. | Thermally cross-linkable hole-transporting materials for improving hole injection in multilayer blue-emitting phosphorescent polymer light-emitting diodes |