Organotin(IV) complexes with 2-hydroxynaphthaldehyde-N(4)-ethylthiosemicarbazone: Synthesis, characterization, and in vitro antibacterial activity

被引:11
|
作者
Salam, M. A. [1 ]
Arafath, Md. Azharul [2 ]
Hussein, Mouayed A. [3 ]
Basri, Rabeya [1 ]
Pervin, Rehana [2 ]
机构
[1] Bangladesh Petr Explorat & Prod Co Ltd BAPEX, BAPEX Bhabon, 4 Karwan Bazar, Dhaka 1215, Bangladesh
[2] Shahjalal Univ Sci & Technol, Dept Chem, Sylhet, Bangladesh
[3] Univ Basrah, Dept Chem, Coll Sci, Basra, Iraq
关键词
2-Hydroxynaphthaldehyde-N(4)-ethylthiosemicarbazone; organotin(IV) complexes; spectral analyses; crystal structure; antibacterial activity; RAY CRYSTAL-STRUCTURE; SPECTROSCOPIC CHARACTERIZATION; CYTOTOXIC ACTIVITY; METAL-COMPLEXES; TRIORGANOTIN(IV) COMPLEXES; SPECTRAL CHARACTERIZATION; DIORGANOTIN COMPLEXES; ANTITUMOR ACTIVITIES; BIOLOGICAL-ACTIVITY; THIOSEMICARBAZONE;
D O I
10.1080/10426507.2016.1146270
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four new organotin(IV) complexes with 2-hydroxynaphthaldehyde-N(4)-ethylthiosemicarbazone [(H2DNET), (1)] of the type [MeSnCl(DNET] (2), [BuSnCl(DNET)] (3), [PhSnCl(DNET)] (4), and [Ph2Sn(DNET] (5) have been synthesized by the direct reaction of H2DNET (1) with organotin(IV) chloride(s) in the presence of potassium hydroxide in absolute methanol. All the compounds were characterized by elemental analyses, molar conductivity, UV-Vis, IR, H-1, C-13, and Sn-119 NMR spectral studies. The molecular structure of ligand (1) has been confirmed by X-ray single crystal diffraction. Spectroscopic data clearly suggested that Sn(IV) center is coordinated with the ONS tridentate ligand (H2DNET) and exhibits a five-coordinate geometry in solution. Antibacterial studies were carried out in vitro against four bacterial strains. All organotin(IV) compounds (2-5) showed good activity against various bacteria but lower activity than the reference drug (Ciprofloxacin). The results demonstrate that organic groups attached to tin(IV) moiety have significant effect on their biological activities. Among them, diphenyltin(IV) derivative 5 exhibits significantly good activity than the other organotin(IV) derivatives (2-4).
引用
收藏
页码:1101 / 1107
页数:7
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