Literature DB >> 15833330

Synthesis, crystal structure and nuclease activity of a Schiff base copper(II) complex.

Lian-Zhi Li1, Chao Zhao, Tao Xu, Hai-Wei Ji, Yan-Hong Yu, Guang-Qiang Guo, Hui Chao.   

Abstract

A new Schiff base copper(II) complex, Cu(o-VANAHE)(2) (o-VANAHE = 2-(o-vanillinamino)-1-hydroxyethane), has been synthesized and characterized. Single crystal X-ray diffraction results suggest that this complex structure belongs to triclinic crystal system, space group P1 with the following crystallographic parameters: a = 8.819(4) angstroms, b = 10.794(5) angstroms, c = 11.350(5) angstroms, alpha = 70.262(6) degrees, beta = 70.816(6) degrees, gamma = 78.360(6) degrees, V = 955.4(7) angstroms3, Z = 2, D(c) = 1.571 Mg x m(-3), and the final R1 = 0.0393, wR2 = 0.0994 for the observed reflections 2620(I > 2sigma(I)). The molecular geometry is almost coplanar. Viscosity, fluorescence spectroscopy and cyclic voltammetry have been conducted to assess their interaction between this complex and DNA. Results showed that the copper(II) complex can increase DNA's relative viscosity and quench the fluorescence intensity of EB bound to DNA. The adding of DNA to the solution of Cu(o-VANAHE)2 causes a slight decrease in the voltammetric current, as well as a slight shift in the E(1/2) to less negative potential. The interaction between the complex and DNA has also been investigated by submarine gel electrophoresis, interestingly, we found that the copper(II) complex can cleave circular plasmid pBR322 DNA to nicked and linear forms.

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Year:  2005        PMID: 15833330     DOI: 10.1016/j.jinorgbio.2005.01.017

Source DB:  PubMed          Journal:  J Inorg Biochem        ISSN: 0162-0134            Impact factor:   4.155


  3 in total

1.  A bis-chelate o-vanillin-2-ethano-lamine copper(II) complex bearing both imine and amine forms of the ligand.

Authors:  Nataliya Plyuta; Vladimir N Kokozay; Julia A Rusanova; Halyna Buvailo; Evgeny Goreshnik; Svitlana Petrusenko
Journal:  Acta Crystallogr E Crystallogr Commun       Date:  2021-11-09

2.  (E)-2-[(2-Hydroxy-ethyl)iminiometh-yl]-6-methoxy-phenolate.

Authors:  Guo-Xia Tan; Xi-Cheng Liu
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-02-21

Review 3.  Modifications of quinolones and fluoroquinolones: hybrid compounds and dual-action molecules.

Authors:  Joanna Fedorowicz; Jarosław Sączewski
Journal:  Monatsh Chem       Date:  2018-06-07       Impact factor: 1.451

  3 in total

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