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

Wang et al., 2005 - Google Patents

Synthesis and properties of new orange red light‐emitting hyperbranched and linear polymers derived from 3, 5‐dicyano‐2, 4, 6‐tristyrylpyridine

Wang et al., 2005

Document ID
530657158357279834
Author
Wang H
Li Z
Jiang Z
Liang Y
Wang H
Qin J
Yu G
Liu Y
Publication year
Publication venue
Journal of Polymer Science Part A: Polymer Chemistry

External Links

Snippet

Two new orange red light‐emitting hyperbranched and linear polymers, poly (pyridine phenylene) s P1 and P2, were prepared by the Heck coupling reaction. In particular, an A2+ B3 approach was developed to synthesize conjugated hyperbranched polymer P2 via one …
Continue reading at onlinelibrary.wiley.com (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
    • H01L51/0034Organic polymers or oligomers
    • H01L51/0035Organic polymers or oligomers comprising aromatic, heteroaromatic, or arrylic chains, e.g. polyaniline, polyphenylene, polyphenylene vinylene
    • H01L51/0038Poly-phenylenevinylene and derivatives
    • 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
    • H01L51/0034Organic polymers or oligomers
    • H01L51/0043Copolymers
    • 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
    • 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
    • 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
    • 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
    • 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
    • C09K2211/14Macromolecular compounds
    • C09K2211/1441Heterocyclic
    • 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
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/549Material technologies organic PV cells

Similar Documents

Publication Publication Date Title
Tamilavan et al. Synthesis and characterization of indenofluorene‐based copolymers containing 2, 5‐bis (2‐thienyl)‐N‐arylpyrrole for bulk heterojunction solar cells and polymer light‐emitting diodes
Lee et al. Enhanced efficiency of polyfluorene derivatives: Organic–inorganic hybrid polymer light‐emitting diodes
Wang et al. Backbone‐acceptor/pendant‐donor strategy for efficient thermally activated delayed fluorescence conjugated polymers with external quantum efficiency close to 25% and emission peak at 608 nm
Lo et al. Synthesis and electroluminescence properties of white‐light single polyfluorenes with high‐molecular weight by click reaction
Chen et al. Synthesis and characterization of a new series of blue fluorescent 2, 6-linked 9, 10-diphenylanthrylenephenylene copolymers and their application for polymer light-emitting diodes
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
Wu et al. Synthesis and optical and electrochemical properties of novel copolymers containing alternating 2, 3‐divinylquinoxaline and hole‐transporting units
Zhuang et al. High‐efficiency, electrophosphorescent polymers with porphyrin–platinum complexes in the conjugated backbone: Synthesis and device performance
Kim et al. Synthesis and characterization of poly (fluorene)‐based copolymer containing triphenylamine group
Mikroyannidis et al. New poly (p‐phenylene vinylene) derivatives with two oxadiazole rings per repeat unit: Synthesis, photophysical properties, electroluminescence, and metal ion recognition
Li et al. Novel saturated red‐emitting poly (p‐phenylenevinylene) copolymers with narrow‐band‐gap units of 2, 1, 3‐benzothiadiazole synthesized by a palladium‐catalyzed Stille coupling reaction
Jeong et al. Synthesis and characterization of indeno [1, 2‐b] fluorene‐based white light‐emitting copolymer
Wu et al. Bipolar copoly (aryl ether) containing distyrylbenzene, triphenylamine, and 1, 2, 4‐triazole moieties: Synthesis and optoelectronic properties
Wang et al. Stable and good color purity white light‐emitting devices based on random fluorene/spirofluorene copolymers doped with iridium complex
Liu et al. Highly efficient red electroluminescent polymers with dopant/host system and molecular dispersion feature: polyfluorene as the host and 2, 1, 3-benzothiadiazole derivatives as the red dopant
Hsieh et al. Synthesis, photophysics, and electroluminescence of copolyfluorenes containing DCM derivatives
Tsai et al. Hyperbranched luminescent polyfluorenes containing aromatic triazole branching units
Kyu Lee et al. White electroluminescence from a single polyfluorene containing bis‐DCM units
Wang et al. Synthesis and properties of new orange red light‐emitting hyperbranched and linear polymers derived from 3, 5‐dicyano‐2, 4, 6‐tristyrylpyridine
Peng et al. New series of highly phenyl‐substituted polyfluorene derivatives for polymer light‐emitting diodes
Liu et al. Synthesis and optoelectronic properties of silole‐containing polyfluorenes with binary structures
Peng et al. New polyphenylene‐and polyphenylenevinylene‐based copolymers containing triarylpyrazoline units in the main chains
Song et al. Synthesis and characterization of polyfluorenevinylene with cyano group and carbazole unit
Chien et al. White electroluminescence from a single polymer: A blue‐emitting polyfluorene incorporating orange‐emitting benzoselenadiazole segments on its main chain
Yoon et al. Synthesis and characterization of fluorene‐based copolymers containing benzothiadiazole derivative for light‐emitting diodes applications