Organometallic compounds with biologically active molecules:: in vitro antibacterial and antifungal activity of some 1,1′-(dicarbohydrazono) ferrocenes and their cobalt(II), copper(II), nickel(II) and zinc(II) complexes

被引:59
作者
Chohan, ZH [1 ]
Supuran, CT
机构
[1] Bahauddin Zakairya Univ, Dept Chem, Multan, Pakistan
[2] Univ Florence, Dipartimento Chim, Lab Chim Bioinorgan, I-50019 Florence, Italy
关键词
1,1 '-(dicarbohydrazono) ferrocenes; metal complexes; antibacterial; antifungal;
D O I
10.1002/aoc.944
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Some 1,1'-(dicarbohydrazono) ferrocenes have been prepared by condensing 1,1'-diacetylferrocene with either 2-furoic hydrazide, 2-thiophenecarboxylic hydrazide or 2-salicylic hydrazide. All the ligands synthesized were characterized by IR and NMR spectroscopy and elemental analysis data (carbon, hydrogen, nitrogen) and then were used as ligands to react with cobalt(II), copper(II), nickel(II) and zinc(II) metals as chlorides to afford metal complexes having the general formula M(L)Cl-2-IR and electronic spectral data, magnetic moment and elemental analyses were used in the structural investigation of the metal complexes synthesized. The ligands synthesized and their metal(II) complexes have been screened for their in vitro antibacterial activity against Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Pseudomonas aeruginosa, Salmonella typhi, Shigella dysenteriae, Bacillus cereus, Corynebacterium diphtheriae, Staphylococcus aureus and Streptococcus pyogenes bacterial strains and for in vitro antifungal activity against Trichophyton longifusus, Candida albicans, Aspergillus flavus, Microsporum canis, Fusarium solani and Candida glabrata. The results of these studies show the metal complexes to be more antibacterial and antifungal than the uncomplexed ligands. However, the potency of all the ligands synthesized and their metal complexes was lower than that of the standard drugs. Copyright (c) 2005 John Wiley & Sons, Ltd.
引用
收藏
页码:1207 / 1214
页数:8
相关论文
共 44 条
[1]  
AGARWAL RK, 1988, J INDIAN CHEM SOC, V65, P448
[2]  
[Anonymous], 1971, INFRARED SPECTRA COM
[3]  
[Anonymous], MAIN GROUP METAL CHE, DOI DOI 10.1515/MGMC.2002.25.5.291
[4]  
ATTAURRAHMAN, 2001, BIOASSAY TECHNIQUES, P16
[5]  
BALHAUSEN CJ, 1962, INTRO LIGAND FIELD
[6]  
BAUER DJ, 1963, LANCET, V2, P494
[7]   TRANSITION-METAL COMPLEXES OF THIOSEMICARBAZIDE AND THIOSEMICARBAZONES [J].
CAMPBELL, MJM .
COORDINATION CHEMISTRY REVIEWS, 1975, 15 (2-3) :279-319
[8]  
Carlin R.L., 1965, TRANSITION METAL CHE
[9]   Main group metal complexes of semicarbazones and thiosemicarbazones.: A structural review [J].
Casas, JS ;
García-Tasende, MS ;
Sordo, J .
COORDINATION CHEMISTRY REVIEWS, 2000, 209 :197-261
[10]  
Chohan Zahid H., 2001, Metal-Based Drugs, V8, P137, DOI 10.1155/MBD.2001.137