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

Pişkin, 2016 - Google Patents

The novel 2, 6-dimethoxyphenoxy substituted phthalocyanine dyes having high singlet oxygen quantum yields

Pişkin, 2016

Document ID
1595451866135086358
Author
Pişkin M
Publication year
Publication venue
Polyhedron

External Links

Snippet

The synthesis of novel peripheral or non-peripheral tetra-2, 6-dimethoxyphenoxy substituted metal free, zinc (II) and indium (III) phthalocyanines was achieved. The novel compounds were characterized by IR, UV–Vis, 1 H NMR, MALDI-TOF mass spectroscopies and …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • 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
    • C07D487/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains four or more hetero rings
    • 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
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • 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
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
    • C09B67/0034—Mixtures of two or more pigments or dyes of the same type
    • 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
    • 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
    • C09B47/00—Porphines; Azaporphines
    • C09B47/04—Phthalocyanines abbreviation: Pc
    • 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
    • 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

Similar Documents

Publication Publication Date Title
Saka et al. Solvent and central metal effects on the photophysical and photochemical properties of 4-benzyloxybenzoxy substituted phthalocyanines
Pişkin The novel 2, 6-dimethoxyphenoxy substituted phthalocyanine dyes having high singlet oxygen quantum yields
Yanık et al. Peripheral and non-peripheral tetrasubstituted aluminium, gallium and indium phthalocyanines: Synthesis, photophysics and photochemistry
Durmuş et al. Synthesis, photophysical and photochemical properties of tetra-and octa-substituted gallium and indium phthalocyanines
Gürel et al. Synthesis, characterization and investigation of the photophysical and photochemical properties of highly soluble novel metal-free, zinc (II), and indium (III) phthalocyanines substituted with 2, 3, 6-trimethylphenoxy moieties
Çamur et al. Highly singlet oxygen generative water-soluble coumarin substituted zinc (II) phthalocyanine photosensitizers for photodynamic therapy
Camur et al. The first comparison of photophysical and photochemical properties of non-ionic, ionic and zwitterionic gallium (III) and indium (III) phthalocyanines
Chauke et al. Novel gallium (III) phthalocyanine derivatives–Synthesis, photophysics and photochemistry
Goslinski et al. Photophysical properties and photocytotoxicity of novel phthalocyanines–potentially useful for their application in photodynamic therapy
Taştemel et al. Photophysical and photochemical properties of novel metallophthalocyanines bearing 7-oxy-3-(m-methoxyphenyl) coumarin groups
Pişkin et al. Highly soluble 7-oxy-3-(4-methoxyphenyl) coumarin bearing zinc phthalocyanines: Synthesis and investigation of photophysical and photochemical properties
Acar et al. Synthesis, characterization and comparative studies on the photophysical and photochemical properties of peripherally and non-peripherally tetra-substituted zinc (II) phthalocyanines
Öztürk et al. Highly soluble 3, 4-(dimethoxyphenylthio) substituted phthalocyanines: synthesis, photophysical and photochemical studies
Pişkin et al. Synthesis, characterization, photophysical and photochemical properties of 7-oxy-3-methyl-4-phenylcoumarin-substituted indium phthalocyanines
Demirbaş et al. Peripherally and non-peripherally tetra-benzothiazole substituted metal-free zinc (II) and lead (II) phthalocyanines: Synthesis, characterization, and investigation of photophysical and photochemical properties
Nas et al. Novel organosoluble metal-free and metallophthalocyanines bearing triazole moieties: Microwave assisted synthesis and determination of photophysical and photochemical properties
Farajzadeh et al. Comparatively singlet oxygen efficiency by sono-photochemical and photochemical studies of new lutetium (III) phthalocyanines
Göl et al. Investigation of photophysical, photochemical and bovine serum albumin binding properties of novel water-soluble zwitterionic zinc phthalocyanine complexes
Ali et al. Synthesis, characterization, photophysical, and photochemical properties of novel zinc (II) and indium (III) phthalocyanines containing 2-phenylphenoxy units
Demirbaş et al. Synthesis, photophysical and photochemical properties of novel tetra substituted metal free and metallophthalocyanines bearing triazine units
Ke et al. Comparison between non-peripherally and peripherally tetra-substituted zinc (II) phthalocyanines as photosensitizers: Synthesis, spectroscopic, photochemical and photobiological properties
Günsel et al. Peripherally and non-peripherally tetra-HBME (4-hydroxybenzyl methyl ether) substituted metal-free and zinc (II) phthalocyanines: synthesis, characterization, and investigation of photophysical and photochemical properties
Erdoğan et al. Novel phthalocyanines bearing 7-oxy-3-(3, 5-difluorophenyl) coumarin moieties: Synthesis, characterization, photophysical and photochemical properties
Dilber et al. The peripheral and non-peripheral 2H-benzotriazole substituted phthalocyanines: Synthesis, characterization, photophysical and photochemical studies of zinc derivatives
Gürel et al. The novel mesityloxy substituted metallo-phthalocyanine dyes with long fluorescence lifetimes and high singlet oxygen quantum yields