首页> 外文期刊>中国化学:英文版 >Synthesis, Crystal Structure, Fluorescence Property and Antibacterial Activity of Two Unprecedented One-dimensional Chain Metal organic Coordination Polymers: Zn(H-SSA)(Phen)(H20)2 and Cu(H-SSA) (Phen) (H20)2
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Synthesis, Crystal Structure, Fluorescence Property and Antibacterial Activity of Two Unprecedented One-dimensional Chain Metal organic Coordination Polymers: Zn(H-SSA)(Phen)(H20)2 and Cu(H-SSA) (Phen) (H20)2

机译:两种前所未有的一维链状金属有机配位聚合物Zn(H-SSA)(Phen)(H20)2和Cu(H-SSA)(Phen)(H20)2的合成,晶体结构,荧光性质和抗菌活性

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The reaction of 5-sulfosalicylic acid(H3-SSA) with o-phenanthroline(Phen),NaOH,and Mcl2(M=Zn,Cu) affords Zn(H-SSA)(Phen)(H2O)2(1) and Cu(H-SSA)(Phen)(H2O)2 (2),respectively ,compounds 1 and 2 are characterized by elemental analysis,IR,fluorescence spectra and single crystal Xray diffraction analysis.The X-ray diffraction analyses reveal that compounds 1 and 2 are isostructure.The 5-sulfosalicylic acid ligand loses two protons at the sulfo-group and carboxylic group during the reaction.The Zn(II) and Cu(II)ions are sixcoordinated and adopt distorted octahedral geometry,which are surrounded by two N atoms from Phen,two O atoms from two water molecules,one O atom from-SO3 group and one oxygen from carboxylic group of the other H-SSA.Compounds 1 and 2 have unprecedented one-dimensional linear chain formed by a repeating mononuclear structureal unit.which is bridged by H-SSA.The fluorescence intensity of 1 and 2 is stronger than that of Phen and H3-SSA at 400nm.The lowest excited single states of these complexes are assigned as mainly Phen localized 1(π π),The antibacterial activity test shows that compounds 1 and 2 strongly inhibit the growth of Streptococcus haemolyticus,Straphylococcus aureus and Escherichia coli.
机译:5-磺基水杨酸(H3-SSA)与邻菲咯啉(Phen),NaOH和Mcl2(M = Zn,Cu)的反应得到Zn(H-SSA)(Phen)(H2O)2(1)和Cu (H-SSA)(Phen)(H2O)2(2)分别通过元素分析,红外光谱,荧光光谱和单晶X射线衍射分析表征化合物1和2.X射线衍射分析显示化合物1和2是同构结构.5-磺基水杨酸配体在反应过程中在磺基和羧基上失去两个质子.Zn(II)和Cu(II)离子是六配位的并且具有扭曲的八面体几何形状,被两个N包围化合物1和2具有空前的一维线性链,该线性链是由重复的单核结构单元形成的,该苯基来自Phen原子,两个O原子来自两个水分子,一个O原子来自-SO3基,一个氧来自另一个H-SSA的羧基。由H-SSA桥接.400 nm处1和2的荧光强度比Phen和H3-SSA的荧光强度强。这些复合物主要被定为Phen定位的1(ππ)。抗菌活性测试表明,化合物1和2强烈抑制溶血链球菌,金黄色葡萄球菌和大肠杆菌的生长。

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