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A new series of the polydentate Schiff base CuII, CoII, NiII, PdII and ZnII complexes derived from ethylenediamine (eda), diethylenetriamine (dea) and tris(2-aminoethyl)amine (taa) have been prepared by template condensation in MeOH solution, and characterized by i.r., electronic spectral data, elemental analyses, conductivity and magnetic measurements. The 1H- and 13C-n.m.r. and mass spectral data of the NiII, PdII and ZnII complexes have been recorded. In all complexes, some of the chloride ions coordinate to the metal ions. From conductivity measurements, it is shown that the complexes are electrolytes. The NiII, PdII and ZnII complexes have diamagnetic character. In this study, the Schiff base CuII and CoII complexes have sub-normal magnetic moments commensurate with their binuclear or tetranuclear nature. Some show antimicrobial activity against bacteria and yeast. 相似文献
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Ahmed F. M. Sadeek S. A. El-Shwiniy W. H. 《Russian Journal of General Chemistry》2019,89(9):1874-1883
Russian Journal of General Chemistry - The new tetradentate Schiff base N,N′-ethylene bis[1-ethyl-6-fluoro-4-imine-7-(piperazine-1-yl)-quinoline-3-carboxylic acid] (Nor-en) has been... 相似文献
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Two novel bidentate Schiff base ligands, 2-(2-hydroxy-3,5-dichloro/diboromo) benzaldehyde-[4-(3-methyl-3-mesitylcyclobutyl)-1,3-thiazol-2-yl]hydrazone,
L1H, L2H and their transition metal complexes are reported. The new ligands and their complexes have been characterized by elemental
analyses, ΛM, infrared, u.v.–vis, 1H- and 13C-n.m.r. spectroscopy, and magnetic susceptibility measurements. The thermal properties of all complexes have been investigated
by TG technique. The complexes contain two monoanionic, bidentate NO ligands. It was found that all the complexes are mononuclear.
Antimicrobial activities of the ligands and their complexes have been tested against five different microorganisms, and some
of the complexes were found to be active against some of the microorganisms studied. 相似文献
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Two new ligands, 4-hydroxy coumarin-3-thiosemicarbazone (H2L1) and 4-hydroxy coumarin-3-semicarbazone (H2L2) were synthesized and used for the preparation of a series of transition metal complexes (Cr3+, Co2+, Ni2+, Cu2+, and Fe3+), derived from these ligands. These complexes have the forms [ML1Cl2]·nX (1–5) and [ML2Cl]·nX (6–9) (X = H2O or ethanol). The structures of these complexes were elucidated by elemental analyses, IR, UV–Vis, and electrical conductivity, as well as magnetic susceptibility measurements and thermal analyses. IR spectral data indicates that in all complexes, the ligands act as monobasic tridentate, coordinated through keto oxygen or sulfur, azomethine nitrogen and deprotonated phenolic oxygen atom. On the basis of other physicochemical investigations, tetrahedral or square planar geometries are assigned for Cu2+ complexes in monomeric structures. In the case of the Co2+, Ni2+ and Fe3+ complexes, octahedral stereochemistries in monomeric structures are suggested. The dissociation constants of the ligands and the stability constants of their Cu(II), Co(II), Ni(II), and Fe(III) complexes have been also determined using potentiometric pH-metric titration in mixed solvents of dioxane: H2O and DMF: H2O with different ratios and different temperatures. 相似文献
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Nuran Asmafiliz Zeynel Kılıç Aslı Öztürk Yasemin Süzen Tuncer Hökelek Leyla Açık 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):1723-1742
Abstract The condensation reactions of hexachlorocyclotriphosphazene (N3P3Cl6) with mono (1 and 2) and bisferrocenyldiamines (3–5 and 7) resulted in the formation of tetrachloro mono- (8 and 9) and bisferrocenylspirocyclotriphosphazenes (10–13). In addition the tetramorpholino mono- (8a and 9a) and bisferrocenylphosphazenes (10a–12a) were obtained from the reactions of the corresponding tetrachlorophosphazenes (8–12) with excess morpholine. The structures of all the phosphazenes were determined using FTIR, MS, 1H, 13C, and 31P NMR and 2-dimensional NMR techniques. The structures of 9a and 13 were determined by single crystal X-ray diffraction techniques. Cyclic voltammetric investigations of compounds 8a, 9a, and 11a revealed that ferrocene redox centers undergo reversible oxidation. These ferrocenylphosphazenes appear to be quite robust electrochemically. Interactions between the compounds 8a, 9a, 11a, and 12a and pBR322 plasmid DNA were investigated by agarose gel electrophoresis. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfer, and Silicon and the Related Elements for the following free supplemental files: Additional text and figures.] 相似文献
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