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

Chu et al., 2019 - Google Patents

Synthesis and electrochromic properties of cross-linked and soluble conjugated polymers based on 5, 8, 14, 17-tetrabromoquinoxaline [2′, 3': 9, 10] phenanthro [4, 5 …

Chu et al., 2019

Document ID
12565221941399885199
Author
Chu T
Ju X
Han X
Du H
Zhang Y
Zhao J
Zhang J
Publication year
Publication venue
Organic Electronics

External Links

Snippet

Three novel electrochromic copolymers PTPE-1, PTPE-2, and PTPE-3 were synthesized by changing the ratio of donor to acceptor using the Stille coupling polymerization. 5, 8, 14, 17- tetrabromoquinoxaline [2′, 3': 9, 10] phenanthro [4, 5-abc] phenazine (monomer b) was first …
Continue reading at www.sciencedirect.com (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
    • C08G61/126Macromolecular 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
    • 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
    • C08G2261/30Monomer units or repeat units incorporating structural elements in the main chain
    • C08G2261/34Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain
    • C08G2261/344Monomer units or repeat units incorporating structural elements in the main chain incorporating partially-aromatic structural elements in the main chain containing heteroatoms
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GASES [GHG] EMISSION, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/54Material technologies
    • Y02E10/549Material technologies organic PV cells
    • 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
    • C08G2261/31Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
    • 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
    • C08G2261/10Definition of the polymer structure
    • 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
    • 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

Similar Documents

Publication Publication Date Title
Chu et al. Synthesis and electrochromic properties of cross-linked and soluble conjugated polymers based on 5, 8, 14, 17-tetrabromoquinoxaline [2′, 3': 9, 10] phenanthro [4, 5-abc] phenazine as the multifunctionalized acceptor unit
Chua et al. Towards modulating the colour hues of isoindigo-based electrochromic polymers through variation of thiophene-based donor groups
Das et al. Cyclopenta [c] thiophene-based D–A conjugated copolymers: effect of heteroatoms (S, Se, and N) of benzazole acceptors on the properties of polymers
Zhao et al. Three donor-acceptor polymeric electrochromic materials employing 2, 3-bis (4-(decyloxy) phenyl) pyrido [4, 3-b] pyrazine as acceptor unit and thiophene derivatives as donor units
WO2009094361A2 (en) Conjugated polymers from substituted 3,4-propylenedioxythiophene, compositions, method of making, and use thereof
Xu et al. The synthesis of new donor–acceptor polymers containing the 2, 3-di (2-furyl) quinoxaline moiety: Fast-switching, low-band-gap, p-and n-dopable, neutral green-colored materials
Zhang et al. A conjugated polymer with Electron-withdrawing cyano group enables for flexible asymmetric electrochromic supercapacitors
Ye et al. Pyrrolophthalazine dione (PPD)-based donor–acceptor polymers as high performance electrochromic materials
Zhang et al. Synthesis and characterization of novel donor–acceptor type neutral green electrochromic polymers containing an indolo [3, 2-b] carbazole donor and diketopyrrolopyrrole acceptor
Toksabay et al. Thieno [3, 2-b] thiophene as π-bridge at different acceptor systems for electrochromic applications
Yue et al. Soluble neutral green-colored polymers based on propylenedioxythiophene, benzene and thieno [3, 4-b] pyrazine, and their electrochromic properties
Zhang et al. Three novel donor-acceptor type electrochromic polymers containing 2, 3-bis (5-methylfuran-2-yl) thieno [3, 4-b] pyrazine acceptor and different thiophene donors: Low-band-gap, neutral green-colored, fast-switching materials
Chen et al. Electropolymerization of DA type EDOT-based monomers consisting of camphor substituted quinoxaline unit for electrochromism with enhanced performance
Zhang et al. Synthesis and characterization of donor–acceptor type conducting polymers containing benzotriazole acceptor and benzodithiophene donor or s-indacenodithiophene donor
Hu et al. Synthesis of polyether-bridged bithiophenes and their electrochemical polymerization to electrochromic property
Hu et al. Free-standing oligo (oxyethylene)-functionalized polythiophene with the 3, 4-ethylenedioxythiophene building block: electrosynthesis, electrochromic and thermoelectric properties
Cimrová et al. Donor–acceptor copolymers containing bithiophene and dithiophenylthienothiadiazole units with fast electrochromic response
Cheng et al. Synthesis and characterization of novel donor–acceptor type electrochromic polymers containing diketopyrrolopyrrole as an acceptor and propylenedioxythiophene or indacenodithiophene as a donor
Xue et al. Enhanced electrochromic performances of Polythieno [3, 2-b] thiophene with multicolor conversion via embedding EDOT segment
Göker et al. The effect of the different donor units on fluorescent conjugated polymers containing 2, 1, 3-benzooxadiazole as the acceptor unit
Pola et al. Synthesis of fluorinated benzotriazole (BTZ)-and benzodithiophene (BDT)-based low-bandgap conjugated polymers for solar cell applications
Yasa et al. Selenophene-bearing low-band-gap conjugated polymers: tuning optoelectronic properties via fluorene and carbazole as donor moieties
Tarkuc et al. Tuning of the neutral state color of the π-conjugated donor–acceptor–donor type polymer from blue to green via changing the donor strength on the polymer
WO2018211286A1 (en) N-type conjugated polymers
Tao et al. Molecular engineering of novel DA conjugated polymers for electrochromic energy storage devices toward enhanced performance