Cadmium (II) macrocyclic Schiff-base complexes containing piperazine moiety: Synthesis, spectroscopic, X-ray structure, theoretical and antibacterial studies

被引:32
|
作者
Keypour, Hassan [1 ]
Mahmoudabadi, Masoumeh [1 ]
Shooshtari, Amir [1 ]
Bayat, Mehdi [1 ]
Mohsenzadeh, Fariba [2 ]
Gable, Robert William [3 ]
机构
[1] Bu Ali Sina Univ, Fac Chem, Hamadan 65174, Iran
[2] Bu Ali Sina Univ, Dept Biol, Lab Plant Cell Biol, Hamadan 65174, Iran
[3] Univ Melbourne, Sch Chem, Melbourne, Vic 3010, Australia
关键词
Macrocyclic Schiff-base complexes; Piperazine moiety; X-ray structures; Antibacterial; DFT; Nature of metal-ligand bond; NBO; EDA; EDA-NOCV; ENERGY DECOMPOSITION ANALYSIS; N-HETEROCYCLIC CARBENE; CRYSTAL-STRUCTURE; ZN(II) COMPLEXES; SILVER(I) COMPLEXES; PHOSPHORUS YLIDES; CHEMICAL-BOND; LIGANDS; BR; CL;
D O I
10.1016/j.molstruc.2017.10.074
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The new Cd(II) macrocyclic Schiff-base complexes were prepared via the metal templated [1 + 1] cyclocondensation of 2,2'-(piperazine-1,4-diyIbis (methylene))dianiline (A) and 2,6-pyridinedicarbaldehyde or 2,6-diacetylpyridine. The products were characterized by elemental analysis, mass spectrometry and spectroscopic methods such as: FT-IR, H-1 and C-13-NMR, the crystal structure of [CdL1(ClO4)(2)](CH3CN) (1) complex was also obtained by single-crystal X-ray crystallography. The complexes were tested for in vitro antibacterial properties against some bacteria. The complexes had antibacterial properties and in some cases were active even more than standards. The geometries of the [CdLn (ClO4)(2)], (n = 1,2) complexes have been optimized at the 8P86/def2-SVP level of theory. Also the nature of Cd -> L-n (n = 1,2) bonds in [CdLn (ClO4)(2)], (n = 1,2) complexes are studied with the help of NBO and Energy decomposition analysis (EDA). Results showed that the nature of metal-ligand bond in the complexes is slightly more electrostatic with a contribution of about 52% in total interaction energy. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:196 / 204
页数:9
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