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首页> 外文期刊>Journal of Molecular Structure >Synthesis, characterization and X-ray crystal structures of Vanadium(IV), Cobalt(III), Copper(II) and Zinc(II) complexes derived from an asymmetric bidentate Schiff-base ligand at ambient temperature
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Synthesis, characterization and X-ray crystal structures of Vanadium(IV), Cobalt(III), Copper(II) and Zinc(II) complexes derived from an asymmetric bidentate Schiff-base ligand at ambient temperature

机译:在室温下衍生自不对称双齿席夫碱配体的钒(IV),钴(III),铜(II)和锌(II)配合物的合成,表征和X射线晶体结构

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An asymmetric bidentate Schiff-base ligand (HL: 2-((allylimino)methyl)phenol) was prepared from reaction of salicylaldehyde and Allylamine. Vanadium(IV), Cobalt(III), Copper(II) and Zinc(II) complexes, VOL2, CoL3, CuL2 and ZnL2 were synthesized from the reaction of VO(acac)(2), CoCl2 center dot 6H(2)O, CuCl2 center dot 2H(2)O and Zn(NO3)(2)center dot 6H(2)O with the bidentate Schiff base ligand (HL: 2-allyliminomethyl-phenol) in methanol at ambient temperature. The ligand and its metal complexes were characterized by elemental analysis (CHN), Fr-IR spectroscopy. In addition, H-1 and C-13 NMR techniques were employed for characterization of the ligand (HL) and diamagnetic complex ZnL2. The molecular structures of all complexes were determined by single crystal X-ray diffraction technique. In the ZnL2 and CuL2 complexes, the metal ion is coordinated by two nitrogen and two oxygen atoms from two Schiff base ligands in an approximately square planar trans-[MN2O2] coordination geometry. In the Vanadium(IV) complex, VOL2, the vanadium center in this structure has a distorted tetragonal pyramidal N2O3 coordination sphere and for Cobalt(III) complex, CoL3, the Co-III ion is six coordinated by three bidentate Schiff base ligands in a distorted octahedral environment. (C) 2014 Elsevier B.V. All rights reserved.
机译:由水杨醛和烯丙胺的反应制备不对称的双齿席夫碱配体(HL:2-((烯丙基)甲基)苯酚)。钒(IV),钴(III),铜(II)和锌(II)配合物是通过VO(acac)(2),CoCl2中心点6H(2)O的反应合成的VOL2,CoL3,CuL2和ZnL2 ,CuCl2中心点2H(2)O和Zn(NO3)(2)O中心点6H(2)O与双齿席夫碱配体(HL:2-烯丙基氨基甲基苯酚)在室温下的甲醇溶液中。通过元素分析(CHN),Fr-IR光谱对配体及其金属配合物进行表征。此外,H-1和C-13 NMR技术用于表征配体(HL)和抗磁性配合物ZnL2。所有配合物的分子结构通过单晶X射线衍射技术确定。在ZnL2和CuL2络合物中,金属离子由来自两个席夫碱配体的两个氮原子和两个氧原子以近似正方形的平面[MN2O2]配位几何结构进行配位。在钒(IV)络合物VOL2中,此结构中的钒中心具有扭曲的四角锥锥形N2O3配位球,而对于钴(III)络合物CoL3,Co-III离子由三个二齿席夫碱配体配位成六个扭曲的八面体环境。 (C)2014 Elsevier B.V.保留所有权利。

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