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

Pu et al., 2011 - Google Patents

New photochromic diarylethenes bearing a pyridine moiety

Pu et al., 2011

Document ID
202323596893181047
Author
Pu S
Yan P
Liu G
Miao W
Liu W
Publication year
Publication venue
Tetrahedron letters

External Links

Snippet

A new class of diarylethenes bearing a pyridine unit has been firstly developed and their properties such as photochromism, fatigue resistance, and fluorescence have been discussed. The pyridine unit was connected directly to the central cyclopentene ring as one …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1007—Non-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K9/00—Tenebrescent materials, i.e. materials for which the range of wavelength for energy absorption is changed as result of excitation by some form of energy
    • C09K9/02—Organic tenebrescent materials
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1018—Heterocyclic compounds
    • C09K2211/1025—Heterocyclic compounds characterised by ligands
    • C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
    • 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

Similar Documents

Publication Publication Date Title
Pu et al. New photochromic diarylethenes bearing a pyridine moiety
Pu et al. Syntheses and optoelectronic properties of four photochromic dithienylethenes
Pu et al. Syntheses and properties of new photochromic diarylethene derivatives having a pyrazole unit
Kuroiwa et al. On‐demand control of the photochromic properties of naphthopyrans
Pu et al. Synthesis and the effects of substitution upon photochromic diarylethenes bearing an isoxazole moiety
Kawai et al. Novel photochromic molecules based on 4, 5-dithienyl thiazole with fast thermal bleaching rate
Wang et al. New photochromic diarylethenes bearing a condensed aromatics moiety
Liu et al. Photochromism of new unsymmetrical isomeric diarylethenes bearing a pyridine group
Liu et al. Photochromism of new 3, 5-position hybrid diarylethene derivatives bearing both thiophene and thiazole moieties
Liu et al. Synthesis and photochromic properties of novel pyridine-containing diarylethenes
Pu et al. Photochromism of new diarylethenes bearing both thiazole and benzene moieties
Wang et al. New photochromic 1, 2-diarylperfluorocyclopentenes bearing unsymmetrical six-membered aryl units
Ren et al. A multi‐addressable molecular switch based on a novel diarylethene with an imidazo [4, 5‐f][1, 10] phenanthroline unit
Li et al. Photochromism of novel isomeric diarylethenes with benzofuran and pyridine moieties
Liu et al. New photochromic diarylethenes with a pyrimidine moiety
Pu et al. Modulation of a fluorescence switch based on a photochromic diarylethene and a rhodamine B dye
Wang et al. The effects of heteroaryl ring on the photochromism of diarylethenes with a naphthalene moiety
Jin et al. Novel photochromic and electrochromic diarylethenes bearing triphenylamine units
Li et al. Photochromism of new isomeric pyridine-containing diarylethenes with a benzofuran moiety
Liu et al. The effect of the cyano group position upon unsymmetrical isomeric diarylethenes bearing a pyrrole unit
Chen et al. A fluorescence switch based on a controllable photochromic naphthopyran group
Pu et al. The synthesis of novel photochromic diarylethenes bearing a biphenyl moiety and the effects of substitution on their properties
Sun et al. Synthesis and photochromism of novel unsymmetrical diarylethenes with an azaindole unit
Guo et al. Synthesis and photoswitching behavior of donor-acceptor type dithienylethene derivatives modified by diestervinyl moieties
Li et al. Rapid decoloration and acidichromism of photochromic 3, 3-diaryl-3H-pyrano [3, 2-f] quinolines