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

Tsai et al., 2007 - Google Patents

Novel hyperbranched polyfluorenes containing electron-transporting aromatic triazole as branch unit

Tsai et al., 2007

Document ID
8240727585622233319
Author
Tsai L
Chen Y
Publication year
Publication venue
Macromolecules

External Links

Snippet

Linear (P 1) and hyperbranched polyfluorenes (PF1− PF5) containing hole-transporting [(4- (9-carbazolyl) butoxyphenyl)] side groups and different amounts of branching triphenyl-1, 2, 4-triazole units (mole fraction: 0− 0.22) have been synthesized to investigate hyperbranched …
Continue reading at pubs.acs.org (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
    • 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
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/12Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
    • C08G61/122Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • 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
    • 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

Similar Documents

Publication Publication Date Title
Shu et al. Highly efficient blue-light-emitting diodes from polyfluorene containing bipolar pendant groups
Yang et al. High-efficiency saturated red emitting polymers derived from fluorene and naphthoselenadiazole
Yu et al. Synthesis and Characterization of a New p− n Diblock Light-Emitting Copolymer
Wu et al. Highly efficient light-emitting diodes based on fluorene copolymer consisting of triarylamine units in the main chain and oxadiazole pendent groups
Peng et al. Synthesis and characterization of new red-emitting polyfluorene derivatives containing electron-deficient 2-pyran-4-ylidene− malononitrile moieties
Xia et al. Decreased aggregation phenomena in polyfluorenes by introducing carbazole copolymer units
Liu et al. Effect of cyano substituents on electron affinity and electron-transporting properties of conjugated polymers
Lu et al. Pure deep blue light-emitting diodes from alternating fluorene/carbazole copolymers by using suitable hole-blocking materials
Cho et al. Saturated and efficient red light-emitting fluorene-based alternating polymers containing phenothiazine derivatives
Tsai et al. Novel hyperbranched polyfluorenes containing electron-transporting aromatic triazole as branch unit
Tseng et al. Stable organic blue-light-emitting devices prepared from poly [spiro (fluorene-9, 9 ‘-xanthene)]
Jacob et al. A fully aryl-substituted poly (ladder-type pentaphenylene): A remarkably stable blue-light-emitting polymer
Tang et al. Synthesis of new conjugated polyfluorene derivatives bearing triphenylamine moiety through a vinylene bridge and their stable blue electroluminescence
Liu et al. Thermally cross-linkable hole-transporting materials for improving hole injection in multilayer blue-emitting phosphorescent polymer light-emitting diodes
Liu et al. Synthesis and characterization of a novel light-emitting polymer containing highly efficient hole-transporting aromatic diamine
Aubert et al. Copolymers of 3, 4-ethylenedioxythiophene and of pyridine alternated with fluorene or phenylene units: Synthesis, optical properties, and devices
Su et al. Tuning wavelength: Synthesis and characterization of spiro-DPVF-containing polyfluorenes and applications in organic light-emitting diodes
Meng et al. Facile synthetic route to a novel electroluminescent polymer− poly (p-phenylenevinylene) containing a fully conjugated aromatic oxadiazole side chain
Cao et al. Novel blue-light-emitting truxene-containing hyperbranched and zigzag type copolymers: Synthesis, optical properties, and investigation of thermal spectral stability
Zhan et al. New series of blue-emitting and electron-transporting copolymers based on cyanostilbene
Huang et al. Solution-processable polyphenylphenyl dendron bearing molecules for highly efficient blue light-emitting diodes
Li et al. Novel thieno-[3, 4-b]-pyrazines cored dendrimers with carbazole dendrons: design, synthesis, and application in solution-processed red organic light-emitting diodes
Tonzola et al. A new synthetic route to soluble polyquinolines with tunable photophysical, redox, and electroluminescent properties
Liou et al. A new class of high T g and organosoluble aromatic poly (amine− 1, 3, 4-oxadiazole) s containing donor and acceptor moieties for blue-light-emitting materials
Kamtekar et al. Synthesis and spectroscopy of poly (9, 9-dioctylfluorene-2, 7-diyl-co-2, 8-dihexyldibenzothiophene-S, S-dioxide-3, 7-diyl) s: solution-processable, deep-blue emitters with a high triplet energy