[go: up one dir, main page]

Jang et al., 1998 - Google Patents

Synthesis and characterization of a new polymer containing an electron accepting perfluoro group

Jang et al., 1998

Document ID
15967075980139773243
Author
Jang M
Suh M
Shim S
Shim H
Publication year
Publication venue
Macromolecular Chemistry and Physics

External Links

Snippet

Abstract Poly {oxy‐4, 4′‐octafluorobiphenylyleneoxy‐alt‐[1, 4‐phenylenevinylene (3‐ trimethylsilyl‐1, 4‐phenylene) vinylene‐1, 4‐phenylene]}(PFSi) was synthesized and characterized to investigate its thermal, optical, electrical and xerographic properties. An …
Continue reading at onlinelibrary.wiley.com (other versions)

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
    • H01L51/0043—Copolymers
    • 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
    • H01L51/0032—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
    • 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
    • C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
    • C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic 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
    • H01L51/50—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];
    • 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

Similar Documents

Publication Publication Date Title
Liang et al. Synthesis and electroluminescent property of poly (p-phenylenevinylene) s bearing triarylamine pendants
US6399224B1 (en) Conjugated polymers with tunable charge injection ability
US5741921A (en) Conjugated polymers containing hetero-spiro atoms and their use as electroluminescence materials
Gupta et al. Band-gap tuning of pendant polymers for organic light-emitting devices and photovoltaic applications
JP2005528492A (en) Copolymers with tunable energy levels and emission colors
EP2520576A1 (en) Compound and organic electroluminescent element using said compound
Wu et al. Enhancing the thermal and spectral stabilities of polyfluorene-based blue-light-emitting materials by incorporating pendent spiro-cycloalkyl groups
Liu et al. Synthesis and characterization of new poly (cyanoterephthalylidene) s for light-emitting diodes
Tang et al. Synthesis, electroluminescence, and photovoltaic properties of dendronized poly (p-phenylene vinylene) derivatives
US7115899B2 (en) Light-emitting copolymers and electronic devices using such copolymers
Jaballah et al. Blue-luminescent poly (p-phenylenevinylene) derivatives: Synthesis and effect of side-group size on the optical properties
Jeong et al. Synthesis and characterization of indeno [1, 2‐b] fluorene‐based white light‐emitting copolymer
US20050119491A1 (en) 2, 7-Substituted carbazoles and oligomers, polymers and co-polymers thereof
Zrida et al. Synthesis and study of morphological, optical and electrical properties of new organic semi conducting polymers containing isosorbide pendant group
Morisaki et al. Novel π-conjugated cyclophane polymers containing phenylamine moieties with strong blue-light emission
Hwang et al. Light-emitting properties of a germyl-substituted PPV derivative synthesized via a soluble precursor
Park et al. Synthesis and electroluminescent properties of bis (3-N-ethylcarbazolyl) cyanoterephthalidene
Jang et al. Synthesis and characterization of a new polymer containing an electron accepting perfluoro group
Islam et al. Highly emissive fluorene and thiophene based π-conjugated A-alt-B copolymers: Synthesis, characterization and electroluminescence properties
Huang et al. Highly efficient electroluminescent biphenylyl-substituted poly (p-phenylenevinylene) s through fine tuning the polymer structure
Zhang et al. Efficient Blue Light-Emitting Diodes Based on Conjugated Polymers with Fluorinated Silole Chemically Doped in Fluorene–Carbazole Main Chain
Karpagam et al. Enhancement of processability, stability and photoluminescence performance of poly (p-phenylene vinylene) containing diazine heterocycle unit
Yamada et al. Synthesis and characterization of fluorene-carbazole and fluorene-phenothiazine copolymers with carbazole and oxadiazole pendants for organic light emitting diodes
Hwang et al. Green electroluminescent diode from poly (2-trimethylsilyl-1, 4-phenylene vinylene)
Jin et al. Novel conjugated polymers employing the binding of polyfluorene derivatives and C60