Nothing Special   »   [go: up one dir, main page]

Gin et al., 1994 - Google Patents

Synthesis and processing of poly (p-phenylene) via the phosphoric acid-catalyzed pyrolysis of a stereoregular precursor polymer: a characterization study

Gin et al., 1994

View PDF
Document ID
3186363778811412999
Author
Gin D
Avlyanov J
MacDiarmid A
Publication year
Publication venue
Synthetic metals

External Links

Snippet

Flexible, free-standing films of high molecular weight, structurally regular poly (p- phenylene)(PPP) were prepared via the thermal conversion of a stereoregular precursor polymer using o-phosphoric acid as an aromatization catalyst. Approximately 83–90 wt.% of …
Continue reading at www.sciencedirect.com (PDF) (other versions)

Classifications

    • 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
    • C08G61/123Macromolecular 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
    • C08G61/124Macromolecular 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
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12Organic substances
    • H01B1/124Intrinsically conductive polymers
    • H01B1/128Intrinsically conductive polymers comprising six-membered aromatic rings in the main chain, e.g. polyanilines, polyphenylenes
    • HELECTRICITY
    • H01BASIC ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B1/00Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
    • H01B1/06Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
    • H01B1/12Organic substances
    • H01B1/124Intrinsically conductive polymers
    • H01B1/125Intrinsically conductive polymers comprising aliphatic main chains, e.g. polyactylenes
    • 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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/22Polybenzoxazoles
    • 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
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/02Polyamines
    • C08G73/026Wholly aromatic polyamines
    • C08G73/0266Polyanilines or derivatives thereof
    • 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
    • C08G79/00Macromolecular compounds obtained by reactions forming a linkage containing atoms other than silicon, sulfur, nitrogen, oxygen, and carbon with or without the latter elements in the main chain of the macromolecule
    • 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
    • C08G75/00Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
    • 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
    • C08G69/00Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids

Similar Documents

Publication Publication Date Title
Palaniappan et al. Temperature effect on conducting polyaniline salts: Thermal and spectral studies
Shacklette et al. Conducting complexes of polyphenylene sulfides
Han et al. Protonic acids: Generally applicable dopants for conducting polymers
Angelopoulos et al. Polyaniline: processability from aqueous solutions and effect of water vapor on conductivity
Pomerantz et al. Processable polymers and copolymers of 3-alkylthiophenes and their blends
Gin et al. Synthesis and processing of poly (p-phenylene) via the phosphoric acid-catalyzed pyrolysis of a stereoregular precursor polymer: a characterization study
Wang et al. Studies on Conjugated Polymers: Preparation, Spectroscopic, and Charge-Transport Properties of a New Soluble Polythiophene Derivative: Poly (3', 4'-dibutyl-2, 2': 5', 2''-terthiophene)
Yang et al. Chitaline materials: soluble chitosan-polyaniline copolymers and their conductive doped forms
Sato et al. Preparation and properties of poly (p‐phenylene) and polynaphthylene
US4618453A (en) Conductive heterocyclic ladder polymers
Lee et al. A novel conducting soluble polypyrrole composite with a polymeric co-dopant
Abraham et al. Highly conducting polymer blend films of polyaniline and nylon 6 by cosolvation in an organic acid
Gal et al. Electrical conductivity and spectral properties of iodine‐doped poly (2‐ethynylpyridine)
US4727135A (en) Synthesis of polyquinoline by the catalytical dehydrogenative polymerization of tetrahydroquinoline
Kim et al. Electrical conductivity change of polyaniline–dodecyl benzene sulfonic acid complex with temperature
Massoumi et al. Chemical and electrochemical grafting of polythiophene onto polystyrene synthesized via ‘living’anionic polymerization
Jiang et al. Iodine-doped poly (ethylenepyrrolediyl) derivatives: a new class of nonconjugated conducting polymers
Kang et al. Halogen induced polymerization of furan
Yang et al. Inverse emulsion polymerization for high molecular weight and electrically conducting polyanilines
Laakso et al. Synthesis and characterization of conducting polymer blends of poly (3-alkylthiophenes)
Amarnath et al. Polyaniline doped by a new class of dopants, benzoic acid and substituted benzoic acid: synthesis and characterization
Mertens et al. Characterization and dc conductivity of poly (p-phenylene vinylene) films doped with FeCl3
Jin et al. Synthesis and Characterization of Poly [(2-(2-phenylethenyl)-1, 4-phenylene) vinylene], Poly [(2-methoxy-5-(2-phenylethenyl)-1, 4-phenylene) vinylene], and Their Copolymers Containing 1, 4-Phenylenevinylene Units
Kulkarni et al. Investigation of effect of protonic acid media on the optical and thermal properties of chemically synthesized poly (o-toluidine)
Wilbur et al. A representative of a new class of conducting oligomer: acetylene-terminated polyaniline