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

Ertan et al., 2021 - Google Patents

Polyhedral oligomeric silsesquioxane cage integrated soluble and fluorescent poly (3, 4-propylenedioxythiophene) dye

Ertan et al., 2021

Document ID
9615567786995773143
Author
Ertan S
Kaya M
Cihaner A
Publication year
Publication venue
Polymer

External Links

Snippet

A new analog of poly (3, 4-propylenedioxythiophene) conjugated polymers called PProDOT- POSS, where polyhedral oligomeric silsesquioxane (POSS) nanocage with alkyl substitutions was integrated on the bridge of 3, 4-propylenedioxythiophene unit and its …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • 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
    • H01B1/127Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
    • 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
    • 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
    • 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
    • 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
    • C08G61/126Macromolecular 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 sulfur atom in the ring
    • 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
    • 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
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/32Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
    • C08G2261/322Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
    • C08G2261/3223Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed containing one or more sulfur atoms as the only heteroatom, e.g. thiophene
    • 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
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/90Applications
    • 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
    • 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

Similar Documents

Publication Publication Date Title
Pankow et al. The development of conjugated polymers as the cornerstone of organic electronics
Patra et al. Polyselenophenes
Chen et al. Low potential electrochemical syntheses of heteroaromatic conducting polymers in a novel solvent system based on trifluroborate–ethyl ether
Havinga et al. Absorption Properties of Alkoxy-Substituted Thienylene− Vinylene Oligomers as a Function of the Doping Level
Gribkova et al. Chemical synthesis of polyaniline in the presence of poly (amidosulfonic acids) with different rigidity of the polymer chain
Qin et al. Synthesis and electrochromic properties of polyacrylate functionalized poly (3, 4-ethylenedioxythiophene) network films
Dai et al. Electrochemistry, electrochromic and color memory properties of polymer/copolymer based on novel dithienylpyrrole structure
Shomura et al. Electrochemical generation and spectroscopic characterization of charge carriers within isolated planar polythiophene
Chao et al. New method of synthesis of electroactive polyamide with amine‐capped aniline pentamer in the main chain
Hsiao et al. Fluorescent and electrochromic polymers from 2, 8-di (carbazol-9-yl) dibenzothiophene and its S, S-dioxide derivative
Pei et al. Poly [3-(4-octylphenyl) thiophene], a new processible conducting polymer
Ming et al. Solvent effects on electrosynthesis, morphological and electrochromic properties of a nitrogen analog of PEDOT
Is et al. A new imine coupled pyrrole–carbazole–pyrrole polymer: Electro-optical properties and electrochromism
Thota et al. Dianiline conjugated Schiff base molecule: Electrical and electrochemical properties
Fong et al. Visible light-mediated photoclick functionalization of a conjugated polymer backbone
İçli-Özkut et al. A neutral state yellow to navy polymer electrochrome with pyrene scaffold
Çakal et al. Effect of the donor units on the properties of fluorinated acceptor based systems
Lu et al. Electrochemical polymerization of benzanthrone and characterization of its excellent green-light-emitting polymer
Turkoglu et al. Electropolymerization, spectroelectrochemistry and electrochromic properties of cross-conjugated and conjugated selenophenothiophenes with thiophene bridge
Lu et al. Electrosynthesis of highly conducting poly (1, 5-dihydroxynaphthalene) in BF3· Et2O
Ertan et al. Polyhedral oligomeric silsesquioxane cage integrated soluble and fluorescent poly (3, 4-propylenedioxythiophene) dye
Dong et al. Electrodeposition of conductive poly (3-methoxythiophene) in ionic liquid microemulsions
Lu et al. Electropolymerization study of benzothiophenes and characterization of novel poly (dibenzothiophene-S, S-dioxide)
Holze Spectroelectrochemistry of conducting polymers
Ramírez-Gómez et al. Physicochemical and Luminescent Properties of Copolymers Composed of Three Monomers: Polythiophenes Based on 3‐Hexylthiophene and 3, 4‐Ethylenedioxythiophene