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

Tan et al., 2013 - Google Patents

Syntheses, characterizations and electrochemical properties of mesomorphic 4-(4′-alkoxy-(1, 1′-biphenyl)-4-oxy) butane-1-sulfonic acids

Tan et al., 2013

Document ID
16953167248968300806
Author
Tan S
Wang C
Liang T
Huang W
Wu Y
Publication year
Publication venue
Journal of Molecular Structure

External Links

Snippet

Biphenyl based sulfonic acid derivatives have been synthesized for anhydrous proton conduction. The terminal sulfonic acid moiety was attached to a biphenyl core by ring- opening reaction of 1, 4-butane sultone. The target compounds exhibited smectic phases in …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/06Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/06Non-steroidal liquid crystal compounds
    • C09K19/34Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
    • C09K19/3441Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having nitrogen as hetero atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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 with heteroatoms or with carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals
    • C07D213/79Acids; Esters
    • 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
    • Y02E60/00Enabling technologies or technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage
    • Y02E60/13Ultracapacitors, supercapacitors, double-layer capacitors

Similar Documents

Publication Publication Date Title
KR100579650B1 (en) Liquid crystalline ion conductor and method for preparation thereof
Kumar Playing with discs
Kong et al. Multi-arm ionic liquid crystals formed by pyridine-mesophase and copper phthalocyanine
Tan et al. Anhydrous proton conduction in liquid crystals containing benzimidazole moieties
Ni et al. Truxene discotic liquid crystals with two different ring substituents: synthesis, mesomorphism and high charged carrier mobility
Liu et al. Tunable supramolecular helical aggregate and optoelectrical properties of perylene diimides by stereoisomerism of sugar
Saha et al. Polar switching and cybotactic nematic ordering in 1, 3, 4-thiadiazole-based short-core hockey stick-shaped fluorescent liquid crystals
Yuvaraj et al. Novel electron-deficient phenanthridine based discotic liquid crystals
Akkurt et al. Synthesis and liquid crystalline properties of new triazine-based $\pi $-conjugated macromolecules with chiral side groups
Wang et al. Ionic liquid-crystalline network polymers formed by sulfonic acid-containing polysiloxanes and pyridinium compounds
Orhan et al. Performance analysis and negative dielectric anisotropy behavior of nematic liquid crystal doped with newly synthesized 1-(p-chlorobenzyl)-5-nitrobenzimidazole cobalt complex
Yamashita et al. Use of a protic salt for the formation of liquid-crystalline proton-conductive complexes with mesomorphic diols
Ono et al. Design of 3D continuous proton conduction pathway by controlling co-organization behavior of gemini amphiphilic zwitterions and acids
Qiao et al. Supramolecular thermotropic ionic liquid crystals formed via self-assembled zwitterionic ionic liquids
Guo et al. Room-temperature AIE ionic liquid crystals based on diphenylacrylonitrile-imidazole salts
Tan et al. Syntheses, characterizations and electrochemical properties of mesomorphic 4-(4′-alkoxy-(1, 1′-biphenyl)-4-oxy) butane-1-sulfonic acids
Zheng et al. Liquid-crystalline behavior and ferroelectric property of viologen-based ionic liquid crystals
Wei et al. Synthesis, structural and electrochemical characterization of benzimidazole compounds exhibiting a smectic C liquid crystal phase
Kumar et al. The first examples of discotic liquid crystalline gemini surfactants
Liang et al. Enhancing proton conduction via doping of supramolecular liquid crystals (4-alkoxybenzoic acids) with imidazole
Taga et al. Liquid-crystalline perylene bisimide derivatives bearing an azacrown ether ring complexing with alkaline metal ions
Weng et al. Design, synthesis, and self‐assembly manipulating of polymerized ionic liquids contained imidazolium based on “Jacketing” effect
Zhang et al. Synthesis and characterisation of novel imidazolium‐based ionic liquid crystals with ap‐nitroazobenzene moiety
Yelamaggad et al. Tris (N-salicylideneanilines)[TSANs] exhibiting a room temperature columnar mesophase: synthesis and characterization
Zhou et al. Self-assembly and ionic conductivity of phthalocyanine-containing liquid-crystalline compound films