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  • Küçük Resim
    Öğe
    Metallo phthalocyanines bearing (2-((2-hydroxyethyl) (p-tolyl)amino)ethoxy) and (2-((2-phenoxyethyl) (p-tolyl)amino)ethoxy) phthalonitrile substituents: Synthesis, characterization, aggregation behavior, antioxidant and antibacterial activity
    (Synthetic Metals, 2014) Çelebi, Metin; Ağırtaş, Salih; Özdemir, Sadin; Okumuş, Veysi
    tThe novel phthalonitrile derivatives bearing (2-((2-hydroxyethyl)(p-tolyl)amino)ethoxy) and (2-((2-phenoxyethyl)(p-tolyl)amino)ethoxy)phthalonitrile substituents at peripheral position were preparedby a nucleophilic displacement reaction. Cyclotetramerization of these phthalonitrile derivatives in thepresence of corresponding metal salts gave the new metallophthalocyanines. The novel compounds werecharacterized by using various spectroscopic data. The aggregation investigations carried out in differ-ent concentrations indicate that phthalocyanine compounds do not have any aggregation behavior forthe concentration range of 10−4–10−6M in tetrahydrofuran. In vitro three antioxidant test methods,namely diphenylpicrylhydrazyl radical scavenging activity, metal chelating activity and reducing powerwere used to determine the antioxidant activity of compounds. Compounds were analyzed for theirantibacterial activity against some bacteria by using the disk-diffusion method.
  • Küçük Resim
    Öğe
    New water soluble phenoxy phenyl diazenyl benzoic acid substituted phthalocyanine derivatives: Synthesis, antioxidant activities, atypical aggregation behavior and electronic properties.
    (Dyes and Pigments, 2013) Ağırtaş, Salih; Çelebi, Metin; Gümüş, Selçuk; Özdemir, Sadin; Okumuş, Veysi
    Novel substituted phthalonitrile derivatives were obtained by the reaction of 2-(4-hydroxyphenylazo) benzoic acid and 4,5-dichloro-1,2-dicyanobenzene, or 4-nitrophthalonitrile. Peripherally phenoxy phenyl diazenyl benzoic acid substituted zinc (II) phthalocyanine complexes, and their sodium salts were synthesized and characterized for the first time. The newly synthesized phthalocyanine complexes show excellent solubility in water. The aggregation investigations carried out in different concentrations indicate that phenoxy phenyl diazenyl benzoic acid-substituted phthalocyanine compounds do not have any aggregation behavior for the concentration range of 7.00 _ 10_5e4.38 _ 10_6 M in DMF. The antioxidant activities of DMF solution of compounds were analyzed through radical scavenging, and chelating ability to Fe2ş cation. Additionally, new compounds did not show any antibacterial activity against some selected bacteria cultures. Moreover, the ground-state geometries of the complexes were optimized using density functional theory (DFT) methods at B3LYP/6-31G(d,p) level in order to obtain information about the 3D geometries and electronic structure.