Mohamed Gehad G, Sharaby Carmen M
Chemistry Department, Faculty of Science, Cairo University, Giza, Egypt.
Spectrochim Acta A Mol Biomol Spectrosc. 2007 Apr;66(4-5):949-58. doi: 10.1016/j.saa.2006.04.033. Epub 2006 May 12.
Metal complexes of Schiff base derived from condensation of o-vanilin (3-methoxysalicylaldehyde) and sulfametrole [N(1)-(4-methoxy-1,2,5-thiadiazole-3-yl)sulfanilamide] (H2L) are reported and characterized based on elemental analyses, IR, 1H NMR, solid reflectance, magnetic moment, molar conductance, mass spectra, UV-vis and thermal analysis (TGA). From the elemental analyses data, the complexes were proposed to have the general formulae [M2X3(HL)(H2O)5].yH2O (where M=Mn(II), Co(II), Ni(II), Cu(II), Zn(II) and Cd(II), X=Cl, y=0-3); [Fe2Cl5(HL)(H2O)3].2H2O; [(FeSO4)2(H2L)(H2O)4] and [(UO2)2(NO3)3(HL)(H2O)].2H2O. The molar conductance data reveal that all the metal chelates were non-electrolytes. The IR spectra show that, H2L is coordinated to the metal ions in a tetradentate manner with ON and NO donor sites of the azomethine-N, phenolic-OH, enolic sulphonamide-OH and thiadiazole-N. From the magnetic and solid reflectance spectra, it is found that the geometrical structures of these complexes are octahedral. The thermal behaviour of these chelates shows that the hydrated complexes losses water molecules of hydration in the first step followed immediately by decomposition of the anions and ligand molecules in the subsequent steps. The activation thermodynamic parameters, such as, E*, DeltaH*, DeltaS* and DeltaG* are calculated from the DrTG curves using Coats-Redfern method. The synthesized ligand, in comparison to their metal complexes also were screened for their antibacterial activity against bacterial species, Escherichia coli, Salmonella typhi, Bacillus subtillus, Staphylococcus aureus and Fungi (Aspergillus terreus and Aspergillus flavus). The activity data show that the metal complexes to be more potent/antimicrobial than the parent Shciff base ligand against one or more microbial species.
报道了由邻香草醛(3 - 甲氧基水杨醛)与磺胺甲噁唑[N(1)-(4 - 甲氧基 - 1,2,5 - 噻二唑 - 3 - 基)磺胺]缩合得到的席夫碱的金属配合物,并通过元素分析、红外光谱、核磁共振氢谱、固体反射光谱、磁矩、摩尔电导率、质谱、紫外可见光谱和热分析(热重分析)对其进行了表征。根据元素分析数据,推测这些配合物的通式为[M2X3(HL)(H2O)5].yH2O(其中M = Mn(II)、Co(II)、Ni(II)、Cu(II)、Zn(II)和Cd(II),X = Cl,y = 0 - 3);[Fe2Cl5(HL)(H2O)3].2H2O;[(FeSO4)2(H2L)(H2O)4]和[(UO2)2(NO3)3(HL)(H2O)].2H2O。摩尔电导率数据表明所有金属螯合物均为非电解质。红外光谱显示,H2L以四齿方式与金属离子配位,通过偶氮甲碱 - N、酚羟基、烯醇式磺酰胺 - OH和噻二唑 - N的ON和NO供体位点配位。从磁光谱和固体反射光谱发现,这些配合物的几何结构为八面体。这些螯合物的热行为表明,水合配合物在第一步失去水分子,随后阴离子和配体分子在后续步骤中分解。使用Coats - Redfern方法从微商热重曲线计算活化热力学参数,如E*、ΔH*、ΔS和ΔG。还对合成的配体及其金属配合物针对细菌物种大肠杆菌、伤寒沙门氏菌、枯草芽孢杆菌、金黄色葡萄球菌以及真菌(土曲霉和黄曲霉)进行了抗菌活性筛选。活性数据表明,金属配合物对一种或多种微生物物种的抗菌活性比母体席夫碱配体更强。