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Articles 31 - 34 of 34
Full-Text Articles in Physical Sciences and Mathematics
Water-Soluble Phthalocyanines Containing Azo Dye; Microwave-Assisted Synthesis And Photochemical Properties Of Znpcs, Ci̇han Kantar, Emrah Ataci, Selami̇ Şaşmaz
Water-Soluble Phthalocyanines Containing Azo Dye; Microwave-Assisted Synthesis And Photochemical Properties Of Znpcs, Ci̇han Kantar, Emrah Ataci, Selami̇ Şaşmaz
Turkish Journal of Chemistry
Novel water-soluble metallophthalocyanines (M: Co, Ni, Cu, Zn) containing azo dye were characterized. The structures were confirmed by IR, UV/vis, ^1H NMR, ^{13}C NMR, mass spectroscopy, and elemental analysis. Photochemical properties and aggregation behavior of zinc phthalocyanines were investigated. Singlet oxygen quantum yields of the zinc phthalocyanines (2d, 3d, 5d, and 6d) were 0.8, 0.57, 0.71, and 0.46, respectively.
A Phthalocyanine--Fluorescein Conjugate, İlker Ün, Yunus Zorlu, Hani̇fe İbi̇şoğlu, Fabienne Dumoulin, Vefa Ahsen
A Phthalocyanine--Fluorescein Conjugate, İlker Ün, Yunus Zorlu, Hani̇fe İbi̇şoğlu, Fabienne Dumoulin, Vefa Ahsen
Turkish Journal of Chemistry
A phthalocyanine--fluorescein conjugate was designed and prepared. Its photophysical properties (electronic absorption and fluorescence) were determined and compared with those of an analogous derivative functionalized by a simple triazole without chromophore. It is likely to be used as a theranostic agent in photodynamic therapy.
Symmetric, Twinned, And Double-Decker Phthalocyanines Substituted By Trialkylated Pentaerythritol, Muzaffer Köç, Ayşe Gül Gürek, Fabienne Dumoulin, Vefa Ahsen
Symmetric, Twinned, And Double-Decker Phthalocyanines Substituted By Trialkylated Pentaerythritol, Muzaffer Köç, Ayşe Gül Gürek, Fabienne Dumoulin, Vefa Ahsen
Turkish Journal of Chemistry
Trialkylated pentaerythritol was chosen as a bulky substituent for a set of 3 free-base phthalocyanines: a symmetric, a twinned, and a double-decker derivative. The bulkiness of this substituent lowered the aggregation of the phthalocyanines. The electronic absorptions were comparatively investigated: the twinned phthalocyanine exhibited a significant near-infrared shifted absorption. The neutral radical Eu(III) complex was oxidized by bromine. These 3 phthalocyanines are promising for use as molecular materials.
Synthesis And Properties Of Triazol-5-One Substituted Phthalocyanines By Microwave Irradiation, Bahatti̇n Kahveci̇, Selami̇ Şaşmaz, Musa Özi̇l, Ci̇han Kantar, Başak Koşar, Orhan Büyükgüngör
Synthesis And Properties Of Triazol-5-One Substituted Phthalocyanines By Microwave Irradiation, Bahatti̇n Kahveci̇, Selami̇ Şaşmaz, Musa Özi̇l, Ci̇han Kantar, Başak Koşar, Orhan Büyükgüngör
Turkish Journal of Chemistry
Triazol-5-one substituted phthalocyanines were prepared quickly by the reaction of 4-nitrophthalonitrile with anhydrous metal salts in DBU (1,8-diazabicyclo[5,4,0]undec-7-ene) and DMAE (dimethylaminoethanol) by microwave irradiation. Microwave yields were higher than those of the conventional synthesis methods. All of these complexes are insoluble in polar solvents such as ethanol, ethyl acetate and chloroform. The characterization of the compounds was accomplished by elemental analysis, ^1H NMR (for I and II), ^{13}C NMR (for I and II), IR and UV-Vis spectral data. In addition, the structure of the starting material (I) was determined by single crystal diffraction.