Sun et al., 2015 - Google Patents
Electrosynthesis and characterization of aminomethyl functionalized PEDOT with electrochromic propertySun et al., 2015
- Document ID
- 9863800601045233874
- Author
- Sun H
- Lu B
- Hu D
- Duan X
- Xu J
- Zhen S
- Zhang K
- Zhu X
- Dong L
- Mo D
- Publication year
- Publication venue
- Chinese Journal of Polymer Science
External Links
Snippet
We herein report the electrosynthesis of an aminomethyl functionalized poly (3, 4- ethylenedioxythiophene)(PEDOT) derivative, poly (2′-aminomethyl-3, 4- ethylenedioxythiophene)(PEDOT-MeNH 2), in CH 2 Cl 2-Bu 4 NPF 6 (0.1 mol· L-1) system …
- 229920001609 Poly(3,4-ethylenedioxythiophene) 0 title abstract description 31
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
-
- 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
- C08G61/126—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 sulfur 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
- H01B1/127—Intrinsically conductive polymers comprising five-membered aromatic rings in the main chain, e.g. polypyrroles, polythiophenes
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/54—Material technologies
- Y02E10/549—Material technologies organic PV cells
-
- 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
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/32—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain
- C08G2261/322—Monomer units or repeat units incorporating structural elements in the main chain incorporating heteroaromatic structural elements in the main chain non-condensed
- C08G2261/3223—Monomer 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
-
- 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
- C08G73/00—Macromolecular 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
- C08G73/02—Polyamines
- C08G73/026—Wholly aromatic polyamines
- C08G73/0266—Polyanilines or derivatives thereof
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Lu et al. | Highly stable hybrid selenophene-3, 4-ethylenedioxythiophene as electrically conducting and electrochromic polymers | |
Qin et al. | Synthesis and electrochromic properties of polyacrylate functionalized poly (3, 4-ethylenedioxythiophene) network films | |
Zhen et al. | Tuning the optoelectronic properties of polyfuran by design of furan-EDOT monomers and free-standing films with enhanced redox stability and electrochromic performances | |
Cheng et al. | Star-shaped conjugated systems derived from thienyl-derivatized poly (triphenylamine) s as active materials for electrochromic devices | |
Lu et al. | Electrosynthesis of poly (3, 4-ethylenedithiathiophene) in an ionic liquid and its electrochemistry and electrochromic properties | |
Ming et al. | Solvent effects on electrosynthesis, morphological and electrochromic properties of a nitrogen analog of PEDOT | |
Zhen et al. | Poly (mono-, bi-or trifuran): effect of oligomer chain length on the electropolymerization performances and polymer properties | |
Xu et al. | Triphenylamine-based multielectrochromic material and its neutral green electrochromic devices | |
Nie et al. | Electrodeposition of poly (indole-5-carboxylic acid) in boron trifluoride diethyl etherate containing additional diethyl ether | |
Sezai Sarac et al. | Electrolyte and solvent effects of electrocoated polycarbazole thin films on carbon fiber microelectrodes | |
Qin et al. | Poly (3, 4-dioxythiophene) soft nano-network with a compatible ion transporting channel for improved electrochromic performance | |
Lin et al. | Synthesis and electro-optical properties of new conjugated hybrid polymers from EDOT end-capped dibenzothiophene and dibenzofuran | |
Yadav et al. | Poly (3, 4-ethylenedioxyselenophene): effect of solvent and electrolyte on electrodeposition, optoelectronic and electrochromic properties | |
Hu et al. | Free-standing oligo (oxyethylene)-functionalized polythiophene with the 3, 4-ethylenedioxythiophene building block: electrosynthesis, electrochromic and thermoelectric properties | |
Sun et al. | Electrosynthesis and characterization of aminomethyl functionalized PEDOT with electrochromic property | |
Lin et al. | Effects on the electrochemical and electrochromic properties of 3 linked polythiophene derivative by the introduction of polyacrylate | |
Sun et al. | Electrosynthesis and Characterization of a New Conducting Copolymer from 2’-aminomethyl-3, 4-ethylenedioxythiophene and 3, 4-ethylenedioxythiophene | |
Turkoglu et al. | Electropolymerization, spectroelectrochemistry and electrochromic properties of cross-conjugated and conjugated selenophenothiophenes with thiophene bridge | |
Zhang et al. | A novel multichromic copolymer of 1, 4-bis (3-hexylthiophen-2-yl) benzene and 3, 4-ethylenedioxythiophene prepared via electrocopolymerization | |
Sun et al. | Aqueous electrosynthesis of an electrochromic material based water-soluble EDOT-MeNH2 hydrochloride | |
Hu et al. | Tuning optoelectronic performances for 3-methylselenophene-EDOT hybrid polymer | |
Lu et al. | Electropolymerization of 3, 4-ethylenedithiathiophene in the green binary solvent system of water and ethanol | |
Lu et al. | Effect of electrolytes on the electropolymerization and optoelectronic properties of poly (3-methylselenophene) | |
Xu et al. | Electrosyntheses of high quality poly (5-cyanoindole) films in boron trifluoride diethyl etherate containing additional diethyl ether | |
Zhang et al. | Low-potential electrosynthesis of novel electroactive poly (9-fluorenemethanol) and its electrochromic and blue-light-emitting properties |