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N-(苯并噻唑-2-基)-4-氯苯磺酰胺及其钕(III)和铊(III)配合物的合成、表征与抗菌研究

Synthesis, Characterization and Antibacterial Studies of N-(Benzothiazol-2-yl)-4-chlorobenzenesulphonamide and Its Neodymium(III) and Thallium(III) Complexes.

作者信息

Obasi Lawrence Nnamdi, Oruma Uchechukwu Susan, Al-Swaidan Ibrahim Abdulrazak, Ramasami Ponnadurai, Ezeorah Chigozie Julius, Ochonogor Alfred Ezinna

机构信息

Department of Pure and Industrial Chemistry, University of Nigeria, Nsukka 410001, Nigeria.

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.

出版信息

Molecules. 2017 Feb 22;22(2):153. doi: 10.3390/molecules22020153.

Abstract

-(Benzothiazol-2-yl)-4-chlorobenzenesulphonamide (NBTCS) was synthesized by condensation reaction of 4-chlorobenzenesulphonyl chloride and 2-aminobenzothiazole in acetone under reflux. Neodymium(III) and thallium(III) complexes of the ligand were also synthesized. Both ligand and metal complexes were characterized using UV-Vis, IR, ¹H- and C-NMR spectroscopies, elemental analysis and molar conductance measurement. IR studies revealed that the ligand is tridentate and coordinates to the metal ions through nitrogen and oxygen atoms of the sulphonamide group and nitrogen atom attached to benzothiazole ring. The neodymium(III) complex displays a coordination number of eight while thallium(III) complex displays a coordination number of six. The ligand and its complexes were screened in vitro for their antibacterial activities against strains ( and ), species, and using the agar well diffusion technique. The synthesized compounds were found to be more active against the microorganisms screened relative to ciprofloxacin, gentamicin and co-trimoxazole.

摘要

-(苯并噻唑-2-基)-4-氯苯磺酰胺(NBTCS)通过4-氯苯磺酰氯与2-氨基苯并噻唑在丙酮中回流进行缩合反应合成。还合成了该配体的钕(III)和铊(III)配合物。使用紫外可见光谱、红外光谱、¹H-和¹³C-核磁共振光谱、元素分析和摩尔电导率测量对配体和金属配合物进行了表征。红外研究表明,该配体是三齿的,通过磺酰胺基团的氮和氧原子以及与苯并噻唑环相连的氮原子与金属离子配位。钕(III)配合物的配位数为八,而铊(III)配合物的配位数为六。使用琼脂孔扩散技术在体外筛选了该配体及其配合物对菌株(和)、物种、和的抗菌活性。相对于环丙沙星、庆大霉素和复方新诺明,发现合成的化合物对所筛选的微生物更具活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a09/6155816/450df9e1e7b8/molecules-22-00153-g001.jpg

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