Synthesis, spectroscopic, thermogravimetric and antimicrobial studies of mixed ligands complexes

被引:48
作者
Mahmoud, Walaa H. [1 ]
Mahmoud, Nessma F. [1 ]
Mohamed, Gehad G. [1 ]
El-Sonbati, Adel. Z. [2 ]
El-Bindary, Ashraf A. [2 ]
机构
[1] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt
[2] Damietta Univ, Fac Sci, Dept Chem, Dumyat 34517, Egypt
关键词
Ternary complexes; Thermal analysis; Antimicrobial activity; TRANSITION-METAL-COMPLEXES; VITRO BIOLOGICAL-ACTIVITY; SCHIFF-BASE COMPLEXES; THERMAL CHARACTERIZATION; OXOVANADIUM(IV) COMPLEXES; SUPRAMOLECULAR STRUCTURE; ANTIBACTERIAL ACTIVITY; COORDINATION MODES; AZODYE COMPLEXES; IONS SYNTHESIS;
D O I
10.1016/j.molstruc.2015.04.004
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
An interesting series of mixed ligand complexes have been synthesized by the reaction of metal chloride with guaifenesin (GFS) in the presence of 2-aminoacetic acid (HGly) (1:1:1 molar ratio). The elemental analysis, magnetic moments, molar conductance, spectral (UV-Vis, IR, H-1 NMR and ESR) and thermal studies were used to characterize the isolated complexes. The molecular structure of GFS is optimized theoretically and the quantum chemical parameters are calculated. The IR showed that the ligand (GFS) acts as monobasic tridentate through the hydroxyl, phenoxy etheric and methoxy oxygen atoms and co-ligand (HGly) as monobasic bidentate through the deprotonated carboxylate oxygen atom and nitrogen atom of amino group. The molar conductivities showed that all the complexes are non-electrolytes except Cr(III) complex is electrolyte. Electronic and magnetic data proposed the octahedral structure for all complexes under investigation. ESR spectrum for Cu(II) revealed data which confirm the proposed structure. Antibacterial screening of the compounds were carried out in vitro on gram positive (Bacillus subtilis and Staphylococcus aureus), gram negative (Escherichia coli and Neisseria gonorrhoeae) bacteria and for in vitro antifungal activity against Candida albicans organism. However, some complexes showed more chemotherapeutic efficiency than the parent GFS drug. The complexes were also screened for their in vitro anticancer activity against the breast cell line (MFC7) and the results obtained showed that they exhibit a considerable anticancer activity. (C) 2015 Elsevier B.V. All rights reserved.
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页码:15 / 25
页数:11
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