Synthesis and biological activity of a ferrocenyl ligand derived from thiophenol and its coordination with some transition metals

被引:9
作者
Abd-Elzaher, Mokhles M. [1 ]
Moustafa, Samia A. [1 ]
Mousa, Hanan A. [1 ]
Labib, Ammar A. [1 ]
机构
[1] Natl Res Ctr, Dept Inorgan Chem, Cairo, Egypt
来源
MONATSHEFTE FUR CHEMIE | 2012年 / 143卷 / 06期
关键词
Bioinorganic chemistry; Ligands; Metallocenes; Schiff bases; Transition metal compounds; AMINO-ACIDS; DERIVATIZING REAGENTS; ZINC(II) COMPLEXES; SCHIFF-BASES; X-RAY; PEPTIDES; CHEMISTRY; NICKEL(II); COBALT(II); PROTEINS;
D O I
10.1007/s00706-011-0685-1
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
The new ferrocenyl ligand 1,1'-bis(2,3-dihydro-2-methylbenzo[]thiazol-2-yl)ferrocene was prepared at room temperature from the condensation reaction of 2-aminothiophenol with 1,1'-diacetylferrocene followed by intramolecular Michael-type addition. The prepared ligand forms 1:1 complexes with manganese(II), cobalt(II), nickel(II), copper(II), and zinc(II) in good yield. Characterization of the ligand and its complexes was carried out using IR, H-1 and C-13 NMR, electronic absorption, mass spectra, magnetic susceptibility, molar conductance, and elemental analysis. Biological activity of the ligand and its complexes was assessed against , , , , , and . The results indicated that the ligand is biologically active but the complexes are more active. The Zn and Cu complexes exhibited biological activity comparable to that of chloramphenicol (commercial broad-spectrum antibiotic).
引用
收藏
页码:909 / 915
页数:7
相关论文
共 55 条
[1]
Synthesis, characterization and biological studies of ferrocenyl complexes containing thiophene moiety [J].
Abd-Elzaher, MM ;
Hegazy, WH ;
Gaafar, AEDM .
APPLIED ORGANOMETALLIC CHEMISTRY, 2005, 19 (08) :911-916
[2]
Synthesis and spectroscopic characterization of some ferrocenyl Schiff bases containing pyridine moiety and their complexation with cobalt, nickel, copper and zinc [J].
Abd-Elzaher, MM .
JOURNAL OF THE CHINESE CHEMICAL SOCIETY, 2004, 51 (03) :499-504
[3]
Synthesis, characterization, and antimicrobial activity of cobalt(II), nickel(II), copper(H) and zinc(II) complexes with ferrocenyl Schiff bases containing a phenol moiety [J].
Abd-Elzaher, MM .
APPLIED ORGANOMETALLIC CHEMISTRY, 2004, 18 (04) :149-155
[4]
Biological studies of newly synthesized ferrocenyl complexes containing triazinone moiety [J].
Abd-Elzaher, Mokhles M. ;
El-shiekh, Said M. ;
Eweis, Mohamed .
APPLIED ORGANOMETALLIC CHEMISTRY, 2006, 20 (10) :597-602
[5]
Synthesis, characterization, and anticancer properties of ferrocenyl complexes containing a salicylaldehyde moiety [J].
Abd-Elzaher, Mokhles M. ;
Moustafa, Samia A. ;
Labib, Ammar A. ;
Ali, Mamdouh M. .
MONATSHEFTE FUR CHEMIE, 2010, 141 (04) :387-393
[6]
Development of organometallic (organo-transition metal) pharmaceuticals [J].
Allardyce, CS ;
Dorcier, A ;
Scolaro, C ;
Dyson, PJ .
APPLIED ORGANOMETALLIC CHEMISTRY, 2005, 19 (01) :1-10
[7]
New orally active non-peptide fibrinogen receptor (GpIIb-IIIa) antagonists: Identification of ethyl 3-[N-[4-[4-[amino[(ethoxycarbonyl)imino]methyl]phenyl]-1,3-thiazol-2-yl]-N-[1-[(ethoxycarbonyl)methyl]piperid-4-yl]amino]propionate (SR 121787) as a potent and long-acting antithrombotic agent [J].
Badorc, A ;
Bordes, MF ;
deCointet, P ;
Savi, P ;
Bernat, A ;
Lale, A ;
Petitou, M ;
Maffrand, JP ;
Herbert, JM .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (21) :3393-3401
[8]
Synthesis of chiral chromium tricarbonyl labeled thymine PNA monomers via the Ugi reaction [J].
Baldoli, C ;
Maiorana, S ;
Licandro, E ;
Zinzalla, G ;
Perdicchia, D .
ORGANIC LETTERS, 2002, 4 (24) :4341-4344
[9]
Incorporation of the unnatural organometallic amino acid 1′-aminoferrocene-1-carboxylic acid (Fca) into oligopeptides by a combination of Fmoc and Boc solid-phase synthetic methods [J].
Barisic, Lidija ;
Rapic, Vladimir ;
Metzler-Nolte, Nils .
EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, 2006, (20) :4019-4021
[10]
Transition-metal receptor systems for the selective recognition and sensing of anionic guest species [J].
Beer, PD .
ACCOUNTS OF CHEMICAL RESEARCH, 1998, 31 (02) :71-80