Synthesis, photophysical and antioxidant properties of carbazole-based bis-thiosemicarbazones

被引:23
作者
Bingul, Murat [1 ]
Senkuytu, Elif [2 ]
Saglam, Mehmet F. [2 ]
Boga, Mehmet [3 ]
Kandemir, Hakan [4 ]
Sengul, Ibrahim F. [2 ]
机构
[1] Dicle Univ, Fac Pharm, Dept Pharmaceut Chem, TR-21280 Diyarbakir, Turkey
[2] Gebze Tech Univ, Dept Chem, Fac Sci, Kocaeli, Turkey
[3] Dicle Univ, Dept Pharmaceut Technol, Fac Pharm, TR-21280 Diyarbakir, Turkey
[4] Namik Kemal Univ, Fac Art & Sci, Dept Chem, Tekirdag, Turkey
关键词
Carbazole; Thiosemicarbazone; Antioxidant activities; Photophysical properties; LIGAND SYNTHESIS; FLUORESCENCE; DERIVATIVES; COPPER(II); COMPLEXES; IRON;
D O I
10.1007/s11164-019-03844-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Utilizing Schiff base condensation of the 9-ethylcarbazole-3,6-dicarbaldehyde and thiosemicarbazides, four new N-ethylcarbazole-based bis-thiosemicarbazone compounds 4a-d were successfully synthesized in high yields. The photophysical properties of the targeted compounds 4a-d were investigated using UV-vis absorption and fluorescence emission spectroscopy. The antioxidant properties of targeted compounds 4a-d were determined by DPPH radical scavenging, ABTS Cation Radical Decolarization and CUPRAC Cupric Reducing Antioxidant Capacity assay methods. Moreover, the anti-cholinesterase properties of designated compounds were investigated by the Acetylcholinesterase (Ach) and Butyrylcholinesterase (BCh) enzyme inhibition assays. The compound 4a was determined as a valuable candidate to be a potent antioxidant agent for the DPPH and ABTS assays. The compound 4d was found to be a target compound for the kinetic measurements to identify the mechanism of action in the area of anticholinesterase activity assay.
引用
收藏
页码:4487 / 4499
页数:13
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