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Full-Text Articles in Physical Sciences and Mathematics
Synthesis And Antioxidant, Aggregation, And Electronic Properties Of6-Tert-Butyl-1,4-Benzodioxine Substituted Phthalocyanines, Mehmet Sali̇h Ağirtaş, Beyza Cabi̇r, Selçuk Gümüş, Sadi̇n Özdemi̇r, Abdurrahman Dündar
Synthesis And Antioxidant, Aggregation, And Electronic Properties Of6-Tert-Butyl-1,4-Benzodioxine Substituted Phthalocyanines, Mehmet Sali̇h Ağirtaş, Beyza Cabi̇r, Selçuk Gümüş, Sadi̇n Özdemi̇r, Abdurrahman Dündar
Turkish Journal of Chemistry
As a starting material, 7-tert-butyldibenzo [b,e] [1,4] dioxine-2,3-dicarbonitrile was prepared by the reac- tion of 4-tert-butylcatechol with 4,5-dichlorophthalonitrile. Metallophthalocyanine complexes 4-7 were obtained by cyclotetramerization of 7-tert-butyldibenzo [b,e] [1,4] dioxine-2,3-dicarbonitrile. All compounds were characterized by elemental analysis and other spectroscopic methods (IR, UV/Vis, and $^{1}$H NMR). Phthalocyanine compounds remained nonaggregated in tetrahydrofuran at the studied concentration ranges. Metallophthalocyanines 4-7 were tested for their antioxidant activities. The antioxidant activity processes included evaluation of radical-scavenging activity, chelat- ing activity, and reducing power. These compounds were compared to standard antioxidant ascorbic acid. The electronic data of the new compounds were obtained by computational …
Synthesis And Biological Evaluation Of Quinoline-Triazole And Quinolone-Triazole Conjugates, Ayşegül Gümüş, Veysi̇ Okumuş
Synthesis And Biological Evaluation Of Quinoline-Triazole And Quinolone-Triazole Conjugates, Ayşegül Gümüş, Veysi̇ Okumuş
Turkish Journal of Chemistry
One-pot synthesis of novel quinoline- and quinolone-substituted 1,2,3-triazoles has been performed from the key intermediates, quinoline- and quinolone-substituted propargyl derivatives 1-3 (48%-88% yields). The antioxidant properties of the newly synthesized compounds, 1a-1c, 2a-2c, and 3a-3c, were evaluated by monitoring DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging abilities, metal chelating effects, and reducing power. The scavenging effects of compounds on the free radical decreased in the order of 3b$>$ 3a$>$ 1b} and were found to be 36.3%, 34.9%, and 27.6% at the concentration of 500 $\mu $g/mL, respectively. All of the compounds showed low chelating capacity. Furthermore, the antibacterial activity was studied …
Synthesis Of 2-Substituted 8-Propargyloxyquinoline Derivatives And Determination Of Their Antioxidant, Antibacterial, And Dna Binding Activities, Ayşegül Gümüş, Veysi̇ Okumuş, Selçuk Gümüş
Synthesis Of 2-Substituted 8-Propargyloxyquinoline Derivatives And Determination Of Their Antioxidant, Antibacterial, And Dna Binding Activities, Ayşegül Gümüş, Veysi̇ Okumuş, Selçuk Gümüş
Turkish Journal of Chemistry
2-Substituted 8-propargyloxyquinoline derivatives have been synthesized from 2-substituted-8-hydroxyquinolines by O-propargylation method (30%-98% yields). The newly synthesized compounds were tested for in vitro antioxidant activities such as DPPH radical scavenging, ferrous chelating, and reducing power activities. The maximum radical scavenging (46.5%) and reducing power activities were obtained from 1 and maximum ferrous chelating effect was obtained from 6 (72.1%) at the concentration of 500 $\mu $g/mL. To indicate DNA binding activity of the complexes calf thymus DNA was used. The compounds were also evaluated for their antimicrobial activity against three gram-positive and three gram-negative bacteria. Compounds 3 and 5 exhibited antibacterial …