Bis-diorganotin(IV) complexes with binucleating hydrazones derived from a methylene-bis-aromatic aldehyde as linker: Synthesis, spectral and structural characterization, antibacterial activity and DNA cleavage studies
首页> 外文期刊>Journal of Organometallic Chemistry >Bis-diorganotin(IV) complexes with binucleating hydrazones derived from a methylene-bis-aromatic aldehyde as linker: Synthesis, spectral and structural characterization, antibacterial activity and DNA cleavage studies
【24h】

Bis-diorganotin(IV) complexes with binucleating hydrazones derived from a methylene-bis-aromatic aldehyde as linker: Synthesis, spectral and structural characterization, antibacterial activity and DNA cleavage studies

机译:Bis-Diorgorinin(iv)与甲基双芳族醛作为接头的亚核酰胺的络合物:合成,光谱和结构表征,抗菌活性和DNA切割研究

获取原文
获取原文并翻译 | 示例
           

摘要

AbstractTwo bis-hydrazone, H4Laand H4Lb, have been synthesized from reaction of 5,5′-methylene-bis-salicylaldehyde with benzhydrazide and furan-2-carbohydrazide, respectively. New organotin(IV) complexes, (R2Sn)2L [L?=?La: R?=?Me (1), Ph (2); L?=?Lb: R?=?Me (3), Ph (4)] have been synthesized by reaction of dihydrazone ligands with R2SnCl2(R?=?Me or Ph). The synthesized compounds have been investigated by elemental analysis and IR,1H NMR, and119Sn NMR spectroscopy. The structures of1and2have been also confirmed by X-ray crystallography. The results show that the dihydrazone acts as a tetrabasic ligand in the enolic form and is coordinated to two SnR2moieties via ONO donor domains by the imine nitrogen and phenolic and enolic oxygen atoms. All complexes are binuclear and the coordination number of both tin is five. Thein?vitroantibacterial activity of ligands and complexes has been evaluated against Gram-positive (Bacillus subtilisandStaphylococcus aureus) and Gram-negative (Escherichia coliandPseudomonas aeruginosa) bacteria and compared with standard drugs. The synthesized compoun
机译:<![CDATA [ 抽象 两个双氢肼,h 4 l a 和h 4 l b < / Ce:sup>,已从5,5'-甲基 - 双水杨醛与苯肼和呋喃-2-碳水化肼的反应合成。新的有机锡(IV)复合物,(R 2 SN) 2 L [l?= ?l a :r?=?me( 1 ),pH( 2 ); l?=?l b :r?=?me( 3 ),ph( 4 )]通过二浦酮配体与R SNCL 2 (r?=?我或pH)。已经通过元素分析和IR来研究合成的化合物, 1 h nmr,以及 119 SN NMR光谱。 1 2 的结构也被X射线晶体学确认。结果表明,二腙作为烯烯型中的四种状配体作用,并与亚胺氮和酚类域通过ONO供体域和inm>部分协调为两个SNR 在β/ ce:斜体>配体和复合物的抗菌活性针对革兰氏阳性(枯草芽孢杆菌和斜体>和金黄色葡萄球菌)和克否定(大肠杆菌假单胞菌Aeruginosa )细菌,与标准药物相比。合成的康乐库

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号