| Literature DB >> 24840495 |
Lan-Qin Chai1, Jiao-Jiao Huang2, Hong-Song Zhang3, Yu-Li Zhang2, Jian-Yu Zhang2, Yao-Xin Li2.
Abstract
An unexpected mononuclear Co(III) complex, [Co(L2)2·(CH3COO)]·CH3OH (HL2=1-(2-{[(E)-3,5-dichloro-2-hydroxybenzylidene]amino}phenyl)ethanone oxime), has been synthesized via complexation of Co(II) acetate tetrahydrate with HL1 originally. The plausible reaction mechanism for the formation of quinazoline-type ligand was proposed. HL1 and its corresponding Co(III) complex were characterized by IR, as well as by elemental analysis and UV-vis spectroscopy. The crystal structure of the complex has been determined by single-crystal X-ray diffraction. Each complex links two other molecules into an infinite 1-D chain via intermolecular hydrogen bonding interactions. Moreover, the electrochemical properties of the cobalt(III) complex were studied by cyclic voltammetry and X-ray photoelectron spectrum (XPS). In addition, superoxide dismutase-like activities of HL1 and Co(III) complex were also investigated.Entities:
Keywords: Crystal structure; Cyclic voltammetry; Quinazoline-type ligand; Spectroscopic behavior; Superoxide dismutase activity; X-ray photoelectron spectrum
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Year: 2014 PMID: 24840495 DOI: 10.1016/j.saa.2014.04.127
Source DB: PubMed Journal: Spectrochim Acta A Mol Biomol Spectrosc ISSN: 1386-1425 Impact factor: 4.098