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

Keum et al., 2004 - Google Patents

Solvatokinetic and solvatochromic behavior of bis (indolinobenzospiropyranyl) sulfide derivatives in various solvents

Keum et al., 2004

View PDF
Document ID
9992270933502072156
Author
Keum S
Ku B
Kim S
Choi Y
Kim S
Koh K
Publication year
Publication venue
Bulletin of the Korean Chemical Society

External Links

Snippet

Solvatokinetic and solvatochromic behavior of bis (indolinobenzospiropyranyl) sulfide derivatives 1a-1c have been studied in various solvents. The marked negative solvatochromism is exhibited for 1a and 1b in the whole region of solvent polarity examined …
Continue reading at koreascience.kr (PDF) (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
    • C07D491/14—Ortho-condensed systems
    • C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B11/00—Diaryl- or thriarylmethane dyes
    • C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
    • C09B11/10—Amino derivatives of triarylmethanes
    • C09B11/24—Phthaleins containing amino groups; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes

Similar Documents

Publication Publication Date Title
Lukyanov et al. Spiropyrans: synthesis, properties, and application.
JP2868262B2 (en) Adamanta / spiroheteroaromatic compound
Ito et al. Prototropic tautomerism and solid-state photochromism of N-phenyl-2-aminotropones
Deligeorgiev et al. Synthesis of photochromic chelating spironaphthoxazines
Shirinian et al. Photo-and PH-switchable fluorescent diarylethenes based on 2, 3-diarylcyclopent-2-en-1-ones with dialkylamino groups
Lvov et al. Revisiting Peri‐Aryloxyquinones: From a Forgotten Photochromic System to a Promising Tool for Emerging Applications
Kim et al. Crystalline-state photochromism and thermochromism of new spiroxazine
Yagi et al. Photochromic properties of cationic merocyanine dyes. Thermal stability of the spiropyran form produced by irradiation with visible light
Tan et al. Synthesis, characterization and photochromic studies in film of heterocycle-containing spirooxazines
Dagilienė et al. Synthesis of 1′, 3, 3′, 4-tetrahydrospiro [chromene-2, 2′-indoles] as a new class of ultrafast light-driven molecular switch
Mahmoodi et al. Synthesis and structure–behavior relationships of tetra-substituted imidazole derivatives of 1, 3-diazabicyclo [3, 1, 0] hex-3-ene
Keum et al. Solvatokinetic and solvatochromic behavior of bis (indolinobenzospiropyranyl) sulfide derivatives in various solvents
El Guesmi et al. Photochromism of dihydroindolizines. Part XXI: multiaddressable photochromic performances based on pyrrolo [1, 2-b] pyridazine photochromes: kinetics, substituent effect and solvatochromism
Keum et al. Synthesis and properties of thermo-and photochromic bisindolinobenzospiropyrans linked by thio-and carbonyl groups
Keum et al. Symmetric and unsymmetric indolinobenzospiropyran dimers: synthesis and characterization
US4139274A (en) Apparatus for changing color
Xie et al. Construction and photoswitching properties of fluorescent diarylethenes
Kikuchi et al. Electronic structure of light-induced lophyl radical derived from a novel hexaarylbiimidazole with π-conjugated chromophore
JP2009024161A (en) Cyanine compound
Watkins et al. Synthesis, characterization, and solvent-independent photochromism of spironaphthooxazine dimers
Laptev et al. Synthesis and study of the photochromic behavior of 3-[6′-nitro-1, 3, 3-trimethylspiro (indolino-2, 2′-[2H]-chromen-5-yl)] propenoic acid and its ethyl ester
CN108752327B (en) 3- (2-benzoxazole) coumarin amide compound and preparation method and application thereof
Jaung et al. Dicyanopyrazine studies. Part V: syntheses and characteristics of chalcone analogues of dicyanopyrazine
Keum et al. Nonactivated Arylazoindolinobenzospiropyran Derivatives. Part 2^ 1: Preparation and Kinetic Measurements of the Spiro-ring Formation from the Merocyanine Form
Chernyshev et al. Biphotochromic and ionochromic benzoxazolyl-substituted spirobipyrans