کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1312022 | 1499145 | 2016 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Synthesis, X-ray structure, spectroscopic, electrochemical properties and DFT calculation of a bridged dinuclear copper(II) complex Synthesis, X-ray structure, spectroscopic, electrochemical properties and DFT calculation of a bridged dinuclear copper(II) complex](/preview/png/1312022.png)
• A bridged dinuclear Cu(II) complex has been synthesized and characterized structurally.
• The spectroscopic data of the Cu(II) complex was compared with the ligand HL1.
• The electrochemical properties of HL1 and the complex have been studied by cyclic voltammetry.
• EPR spectroscopy of the bridged dinuclear Cu(II) complex was also investigated.
• The geometries and electronic properties of both HL1 and the complex were studied by DFT calculation.
A bridged dinuclear Schiff base-type copper(II) complex, [(Cu2(L2)2CH3COO)]2[Cu(NO3)4]·2CH3COOCH2CH3 (HL2 = 1-(2-{[(E)-3,5-dibromo-2-hydroxybenzylidene]amino}phenyl)ethanone oxime), has been synthesized via complexation of Cu(II) nitrate trihydrate with HL1 (2-(3,5-dibromo-2-hydroxyphenyl)-4-methyl-1,2-dihydroquinazoline-3-oxide, H is the deprotonatable hydrogen). During the reaction, the C–N bond in the HL1 is converted into the CN–OH group in the ligand HL2. The Cu(II) complex was analyzed using IR and UV–Vis spectroscopy, elemental analysis and single-crystal X-ray crystallography. The spectroscopic data of the Cu(II) complex was compared with the ligand HL1. In the crystal, each complex links with four other molecules into an infinite 2-D supramolecular structure through intermolecular hydrogen bonding and π⋯π stacking interactions. Moreover, the electrochemical properties of HL1 and Cu(II) complex have been studied by cyclic voltammetry. The powder EPR spectrun of the dinuclear Cu(II) complex indicated that the existence of an antiferromagnetic spin-spin interaction between the magnetically nonequivalent two Cu(II) ions. The geometries and electronic properties of both the ligand HL1 and the Cu(II) complex were studied by DFT calculation.
A bridged dinuclear Schiff base-type copper(II) complex, [(Cu2(L2)2CH3COO)]2[Cu(NO3)4]·2CH3COOCH2CH3 has been synthesized via complexation of Cu(II) nitrate trihydrate with HL1. During the reaction, the C–N bond in the HL1 is converted into the CN–OH group in the ligand HL2. The Cu(II) complex was analyzed using IR and UV–Vis spectroscopy, elemental analysis and single-crystal X-ray crystallography. The spectroscopic data of the Cu(II) complex was compared with the ligand HL1. In the crystal, each complex links with four other molecules into an infinite 2-D supramolecular structure through intermolecular hydrogen bonding and π⋯π stacking interactions. Moreover, the electrochemical properties of HL1 and Cu(II) complex have been studied by cyclic voltammetry. Electron paramagnetic resonance (EPR) spectroscopy of the bridged dinuclear Cu(II) complex was also investigated. The geometries and electronic properties of both the ligand HL1 and the Cu(II) complex were studied by DFT calculation.Figure optionsDownload as PowerPoint slide
Journal: Inorganica Chimica Acta - Volume 444, 1 April 2016, Pages 193–201