Ni(II) and Cu(II) complexes of new unsymmetrical N2O2 Schiff bases derived from 3-(2-aminobenzylimino)-1-phenylbutan-1-ol: synthesis, structure, antibacterial properties, and electrochemistry

被引:8
作者
Meghdadi, Soraia [1 ]
Amirnasr, Mehdi [1 ]
Mereiter, Kurt [2 ]
Motaharipour, Somayeh [1 ]
Nasehi, Monireh [1 ]
Bagheri, Maryam [1 ]
Abbasi, Soheila [3 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan, Iran
[2] Vienna Univ Technol, Fac Chem, A-1040 Vienna, Austria
[3] Univ Isfahan, Dept Biol Sci, Esfahan, Iran
关键词
Unsymmetrical Schiff base; Copper(II) and nickel(II) complexes; Crystal structure; Cyclic voltammetry; Antibacterial activity; TRANSITION-METAL-COMPLEXES; COPPER(II) COMPLEXES; NICKEL(II) COMPLEXES; SPECTROSCOPIC CHARACTERIZATION; CRYSTAL-STRUCTURES; LIGANDS; ANTIFUNGAL; ZN(II); CO(II);
D O I
10.1080/00958972.2015.1085977
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new N2O2 unsymmetrical Schiff bases, H2L1=3-[({o-[(E)-(o-hydroxyphenyl)methylideneamino]phenyl}methyl)imino]-1-phenyl-1-buten-1-ol and H2L2=3-[({o-[(E)-(2-hydroxy-1-naphthyl)methylideneamino]phenyl}methyl)imino]-1-phenyl-1-buten-1-ol, and their copper(II) and nickel(II) complexes, [CuL1] (1), [CuL2] (2), [NiL1] (3), and [NiL2] (4), have been synthesized and characterized by elemental analyses and spectroscopic methods. The crystal structures of these complexes have been determined by X-ray diffraction. The coordination geometry around Cu(II) and Ni(II) centers is described as distorted square planar in all complexes with the CuN2O2 coordination more distorted than the Ni ones. The electrochemical studies of these complexes indicate a good correlation between the structural distortion and the redox potentials of the metal centers. The ligand and metal complexes were also screened for their in vitro antibacterial activity.
引用
收藏
页码:4055 / 4069
页数:15
相关论文
共 38 条
  • [11] Synthesis, spectroscopic characterization, electrochemical behaviour, reactivity and antibacterial activity of some transition metal complexes with 2-(N-salicylideneamino)-3-carboxyethyl-4,5-dimethylthiophene
    Daniel, Varughese P.
    Murukan, B.
    Kumari, B. Sindhu
    Mohanan, K.
    [J]. SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2008, 70 (02) : 403 - 410
  • [12] Elder R. C., 1983, INORG CHEM, V22, P2771
  • [13] Highly efficient chiral copper Schiff-base catalyst for asymmetric cyclopropanation of 2,5-dimethyl-2,4-hexadiene
    Itagaki, M
    Hagiya, K
    Kamitamari, M
    Masumoto, K
    Suenobu, K
    Yamamoto, Y
    [J]. TETRAHEDRON, 2004, 60 (36) : 7835 - 7843
  • [14] The applications of Schiff bases in Ti-catalyzed asymmetric alkynylation of aldehydes
    Jia, Xian
    Yin, Lu
    Zhao, Xuan
    Li, Xing Shu
    [J]. CHINESE CHEMICAL LETTERS, 2007, 18 (03) : 275 - 278
  • [15] Joseyphus R. Selwin, 2008, Mycobiology, V36, P93, DOI 10.4489/MYCO.2008.36.2.093
  • [16] Synthesis, characterization and X-ray crystal structures of copper(II) and nickel(II) complexes with potentially hexadentate Schiff base ligands.
    Khandar, AA
    Hosseini-Yazdi, SA
    Zarei, SA
    [J]. INORGANICA CHIMICA ACTA, 2005, 358 (11) : 3211 - 3217
  • [17] Kwiatkowski E., 1985, J CHEM SOC DA, P803
  • [18] Asymmetric Henry reaction catalyzed by a copper tridentate chiral schiff-base complex
    Lai, Guoyin
    Wang, Sujing
    Wang, Zhiyong
    [J]. TETRAHEDRON-ASYMMETRY, 2008, 19 (15) : 1813 - 1819
  • [19] Lashanizadegan M., 2011, Journal of Sciences-Islamic Republic of Iran, V22, P121
  • [20] Lever A. B. P., 1984, INORGANIC ELECT SPEC, p[565, 535]