[go: up one dir, main page]

Zhang et al., 2017 - Google Patents

Synthesis and application in photovoltaic device of the porphyrin derivatives with liquid crystal properties

Zhang et al., 2017

Document ID
7945500889765231598
Author
Zhang X
Xia Y
Zhou L
Liu P
Deng W
Publication year
Publication venue
Tetrahedron

External Links

Snippet

A series of porphyrin derivatives with four meso-substituted amide groups and their zinc coordination compounds have been synthesized and characterized. The thermal behavior and morphology of these compounds were investigated using thermogravimetry (TG) …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • 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
    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00—Solid 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
    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/005—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene
    • H01L51/0062—Macromolecular systems with low molecular weight, e.g. cyanine dyes, coumarine dyes, tetrathiafulvalene aromatic compounds comprising a hetero atom, e.g.: N,P,S
    • H01L51/0071—Polycyclic condensed heteroaromatic hydrocarbons
    • H01L51/0072—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ringsystem, e.g. phenanthroline, carbazole
    • H—ELECTRICITY
    • H01—BASIC ELECTRIC ELEMENTS
    • H01L—SEMICONDUCTOR DEVICES; ELECTRIC SOLID STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H01L51/00—Solid 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
    • H01L51/0032—Selection of organic semiconducting materials, e.g. organic light sensitive or organic light emitting materials
    • H01L51/0077—Coordination compounds, e.g. porphyrin
    • H01L51/0084—Transition metal complexes, e.g. Ru(II)polypyridine complexes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C-Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom

Similar Documents

Publication Publication Date Title
Sakurai et al. Electron-or hole-transporting nature selected by side-chain-directed π-stacking geometry: liquid crystalline fused metalloporphyrin dimers
Miao et al. Syntheses and characterization of several nickel bis (dithiolene) complexes with strong and broad Near-IR absorption
Chico et al. High one-dimensional charge mobility in semiconducting columnar mesophases of isocyano-triphenylene metal complexes
CN1980791A (en) Perylene n-type semiconductors and related devices
Zhang et al. Synthesis and application in photovoltaic device of the porphyrin derivatives with liquid crystal properties
Huang et al. Dithienopyrrolobenzotriazole-based organic dyes with high molar extinction coefficient for efficient dye-sensitized solar cells
Li et al. Aza-BODIPY dyes with heterocyclic substituents and their derivatives bearing a cyanide co-ligand: NIR donor materials for vacuum-processed solar cells
Chen et al. Boron-and nitrogen-embedded polycyclic arenes as an emerging class of organic semiconductors
Sergeyev et al. Liquid crystalline octaalkoxycarbonyl phthalocyanines: design, synthesis, electronic structure, self-aggregation and mesomorphism
Zhang et al. Synthesis and properties of siloxane modified perylene bisimide discotic liquid crystals
Jeux et al. One step synthesis of DAD chromophores as active materials for organic solar cells by basic condensation
Nishimura et al. Additive-free, cost-effective hole-transporting materials for perovskite solar cells based on vinyl triarylamines
CN103534868B (en) Organic color material and use its dye-sensitized solar cell
Qiu et al. Tuning the central donor core via intramolecular noncovalent interactions based on D (A-Ar) 2 type small molecules for high performance organic solar cells
Duan et al. New organic dyes containing tert-Butyl-capped N-Arylcarbazole moiety for Dye-sensitized solar cells
Umesh et al. Discotic liquid crystalline tris (hexahexyloxytriphenylene) triazines with separate columns of triphenylene and triazine cores
Qiu et al. Electropolymerization and characterization of an alternatively conjugated donor–acceptor metallopolymer: Poly-[Ru (4′-(4-(Diphenylamino) phenyl)-2, 2′: 6′, 2 ″-Terpyridine) 2] 2+
CN103304568B (en) Trimerization Benzazole compounds and its production and use
Zhao et al. Tetradentate platinum (II) complexes: Synthesis, photophysical properties, liquid crystalline characteristics and charge transport behaviour
Xu et al. Synthesis and photochromism of new asymmetrical diarylethenes with a variable heteroaryl ring and a quinoline unit
Xia et al. Synthesis and photovoltaic properties of novel porphyrin derivatives
Huang et al. Dicyanopentafulvene-fused perylene diimide and its stable radical anion
Wang et al. Aryl-bisalkynyl bridged perylene diimides dimers: efficient synthesis, properties and improved electron mobilities
Luo et al. π-Conjugated oligothiophene-anthracene co-oligomers: synthesis, physical properties, and self-assembly
Chen et al. Improving photovoltaic properties of linear small molecules with TPA–DPP segment by tuning their frameworks