Yang et al., 2006 - Google Patents
Highly substituted poly (2, 3‐diphenyl‐1, 4‐phenylenevinylene) derivatives having bulky phenyl and fluorenyl pendant groups: Synthesis, characterization, and electro …Yang et al., 2006
View PDF- Document ID
- 8862164787562915338
- Author
- Yang S
- Li H
- Chen C
- Hsu C
- Publication year
- Publication venue
- Journal of Polymer Science Part A: Polymer Chemistry
External Links
Snippet
Abstract Two series of poly (2, 3‐diphenyl‐1, 4‐phenylenevinylene)(DP‐PPV) derivatives containing multiple bulky substituents were synthesized. In the first series, two different groups were incorporated on C‐5, 6 positions of the phenylene moiety to increase steric …
- -1 poly (2, 3-diphenyl-1, 4-phenylenevinylene) 0 title abstract description 37
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
- H01L51/0034—Organic polymers or oligomers
- H01L51/0035—Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
- H01L51/0039—Polyeflurorene 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
- H01L51/0062—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
-
- 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
- H01L51/0032—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
- H01L51/0034—Organic polymers or oligomers
- H01L51/0043—Copolymers
-
- 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
- H01L51/50—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
- 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
-
- 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
- C09K2211/14—Macromolecular compounds
- C09K2211/1441—Heterocyclic
-
- 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
-
- 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 |
|---|---|---|
| Zhan et al. | New series of blue-emitting and electron-transporting copolymers based on fluorene | |
| US6887972B2 (en) | Blue electroluminescent materials for polymer light-emitting diodes | |
| Mei et al. | Synthesis and characterization of white‐light‐emitting polyfluorenes containing orange phosphorescent moieties in the side chain | |
| Lo et al. | Synthesis and electroluminescence properties of white‐light single polyfluorenes with high‐molecular weight by click reaction | |
| EP1509959A2 (en) | Copolymers having tunable energy levels and color of emission | |
| Zhan et al. | Synthesis and electroluminescence of poly (aryleneethynylene) s based on fluorene containing hole-transport units | |
| Lim et al. | Improved EL efficiency of fluorene‐thieno [3, 2‐b] thiophene‐based conjugated copolymers with hole‐transporting or electron‐transporting units in the main chain | |
| Yang et al. | Synthesis and electroluminescent properties of disubstituted polyacetylene derivatives containing multi‐fluorophenyl and cyclohexylphenyl side groups | |
| Shin et al. | Sterically hindered and highly thermal stable spirobifluorenyl-substituted poly (p-phenylenevinylene) for light-emitting diodes | |
| Chen et al. | Novel poly (2, 3-diphenyl-1, 4-phenylenevinylene) derivatives containing long branched alkoxy and fluorenyl substituents: synthesis, characterization, and their applications for polymer light-emitting diodes | |
| Xiao et al. | Novel green light-emitting polyfluorenes containing dibenzothiophene-S, S-dioxide-arylamine derivatives | |
| Liao et al. | High-performance poly (2, 3-diphenyl-1, 4-phenylene vinylene)-based polymer light-emitting diodes by blade coating method | |
| Peng et al. | Conjugated alternating copolymers of fluorene and 2-pyridine-4-ylidenemalononitrile: synthesis, characterization and electroluminescent properties | |
| Liu et al. | Synthesis and electroluminescent properties of a phenothiazine‐based polymer for nondoped polymer light‐emitting diodes with a stable orange‐red emission | |
| Jeong et al. | Synthesis and characterization of indeno [1, 2‐b] fluorene‐based white light‐emitting copolymer | |
| Kuo et al. | High‐efficiency poly (phenylenevinylene)‐co‐fluorene copolymers incorporating a triphenylamine as the end group for white‐light‐emitting diode applications | |
| Peng et al. | Novel supramolecular polymers based on Zinc‐salen chromophores for efficient light‐emitting diodes | |
| Lin et al. | Novel fluorene-based light-emitting copolymers containing cyanophenyl pendants and carbazole-triphenylamines: Synthesis, characterization and their PLED application | |
| Huang et al. | Synthesis and light emitting properties of polyacetylenes having pendent fluorene groups | |
| Peng et al. | New series of highly phenyl‐substituted polyfluorene derivatives for polymer light‐emitting diodes | |
| Krüger et al. | New organo‐soluble conjugated polyquinolines | |
| Liu et al. | Synthesis and optoelectronic properties of silole‐containing polyfluorenes with binary structures | |
| Rodrigues et al. | Synthesis of a PPV‐fluorene derivative: Applications in luminescent devices | |
| Song et al. | Synthesis and characterization of polyfluorenevinylene with cyano group and carbazole unit | |
| Yang et al. | Highly substituted poly (2, 3‐diphenyl‐1, 4‐phenylenevinylene) derivatives having bulky phenyl and fluorenyl pendant groups: Synthesis, characterization, and electro‐optical properties |