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

Shirota et al., 1984 - Google Patents

Preparation of an electrically conducting polymer by the electrolytic polymerization of N-vinylcarbazole

Shirota et al., 1984

View PDF
Document ID
338785664084726512
Author
Shirota Y
Noma N
Kanega H
Mikawa H
Publication year
Publication venue
Journal of the Chemical Society, Chemical Communications

External Links

Snippet

The controlled-potential anodic oxidation of N-vinylcarbazole in dichloromethane with tetra- n-butylammonium perchlorate as the supporting electrolyte deposited an electrically conducting polymer on the surface of the electrode; the polymer exhibits a room temperature …
Continue reading at citeseerx.ist.psu.edu (PDF) (other versions)

Classifications

    • 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
    • C08G61/124—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 with a five-membered ring containing one nitrogen atom in the ring
    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12—Organic substances
    • H01B1/124—Intrinsically conductive polymers
    • H01B1/125—Intrinsically conductive polymers comprising aliphatic main chains, e.g. polyactylenes
    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12—Organic substances
    • H01B1/124—Intrinsically conductive polymers
    • H01B1/128—Intrinsically conductive polymers comprising six-membered aromatic rings in the main chain, e.g. polyanilines, polyphenylenes
    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12—Organic substances
    • H01B1/124—Intrinsically conductive polymers
    • H01B1/127—Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes

Similar Documents

Publication Publication Date Title
Kaneto et al. Electrochemical preparation of a metallic polythiophene film
Sato et al. Electrochemical preparation of conducting poly (3-methylthiophene): comparison with polythiophene and poly (3-ethylthiophene)
Zagórska et al. Chemical synthesis and characterization of soluble poly (4, 4′-dialkyl-2, 2′-bithiophenes)
Roncali et al. Poly mono-, bi-and trithiophene: Effect of oligomer chain length on the polymer properties
Feldhues et al. Polyalxykothiophenes soluble electrically conducting polymers
US4532188A (en) Electrically conductive pyrrole copolymer article
Siove et al. Chain length effect on the electroactivity of poly (N-alkyl-3, 6-carbazolediyl) thin films
PT85579B (en) PROCESS FOR THE PREPARATION OF ELECTRICALLY CONDUCTIVE SOLUVE POLYMERS
WO1991019021A1 (en) Polymerization of thiophene and its derivatives
Shirota et al. Preparation of an electrically conducting polymer by the electrolytic polymerization of N-vinylcarbazole
US4618454A (en) Conducting polymers
US4663001A (en) Electroconductive polymers derived from heterocycles polycyclic monomers and process for their manufacture
Ferraris et al. Electrochemical and optical properties of thiophene-alkylheteroaromatic copolymers
US4548696A (en) 3,4-Disubstituted polypyrroles and articles of manufacture coated therewith
Miyazaki et al. Characterization, properties and doping of poly (3-alkylthiophene-2, 5-diyl) s, P3RThs (R= n-C6H13, n-C18H17, n-C12H25), prepared by using zero-valent nickel complex
Yamamoto et al. The preparation of poly (dihydroxyphenylene) through the electro-oxidative polymerization of hydroquinone
CA1311715C (en) Method for the electropolymerization of conductive polymers
Qiu et al. Poly [3, 6‐(carbaz‐9‐yl) propanesulfonate]: A Self‐Doped Polymer with Both Cation and Anion Exchange Properties
JPH0794538B2 (en) Novel polymer and method for producing the same
Bolognesi et al. Synthesis and characterization of alkyl-substituted poly (thiophene-2, 5-diylvinylene) s
Mitsuhara et al. Electrochemical preparation of poly (di (2‐thienyl) benzene) s and poly (4, 4′‐di (2‐thienyl) biphenyl)
JPH05262993A (en) Polymer conductor and its production
Jeon et al. Preparation of an electrically conducting polymer by the electrolytic polymerization of 3-vinylperylene
JPH07694B2 (en) Organic semiconductor and manufacturing method thereof
Roncali et al. Recent developments in the synthesis and functionalization of conducting poly (thiophenes)