几种硫代氨基脲配体Cu(II)配合物的微波合成、表征及生物活性研究

K. Verma, N. Nirwan, R. Singh, N. Bhojak
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引用次数: 1

摘要

硫代氨基脲是由硫代氨基脲与羰基化合物缩合而成的一类化合物。硫代氨基脲类过渡金属配合物因其广泛的抗菌、抗肿瘤、抗真菌等生物活性而受到广泛的关注。本文研究了四种新型的Cu(II)芳基硫代氨基脲配合物,其一般组成为[Cu(L1)2Cl2], [Cu(L2)2Cl2], [Cu(L3)2Cl2]和[Cu(L4)2Cl2]{其中L1= 4-硝基苯乙酮硫代氨基脲(4NAT), L2 = 3-硝基苯甲醛硫代氨基脲(3NBT),以硫代氨基脲为原料,采用常规加热法和微波辐照法,与金属铜络合,合成了L3 = 4-羟基苯甲醛硫代氨基脲(4HBT)和L4 = 4-氨基苯乙酮硫代氨基氨基脲(4AAT)。对合成的化合物进行了元素分析、熔点测定、红外光谱、紫外可见光谱等表征。硫代氨基脲配体表现为双齿配体,与Cu(II)形成八面体配合物。合成的配体及其新的金属配合物对大肠杆菌、金黄色葡萄球菌和枯草芽孢杆菌的体外抗菌活性进行了筛选。结果表明,所有Cu(II)配合物都是有效的抑菌剂。
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Microwave Assisted Synthesis, Characterisation and Biological Activities of Cu(II) Complexes of Few Thiosemicarbazones Ligands
Thiosemicarbazones are class of compounds which are obtained by the condensation of thiosemicarbazide with carbonyl compounds. The transition metal complexes of thiosemicarbazones are widely considered due to their broad spectrum of biological activities such as antibacterial, antitumor and antifungal activities. In present research work a series of four novel Cu(II) aryl thiosemicarbazones complexes having the general composition [Cu(L1)2Cl2], [Cu(L2)2Cl2], [Cu(L3)2Cl2] and [Cu(L4)2Cl2]{where L1= 4-nitroacetophenone thiosemicarbazones (4NAT), L2 = 3-nitrobenzaldehyde thiosemicarbazone (3NBT), L3 = 4-hydroxybenzaldehyde thiosemicarbazone (4HBT) and L4 = 4-aminoacetophenone thiosemicarbazone (4AAT)} have been synthesized by the reaction of thiosemicarbazide with substituted aromatic aldehydes and ketones by conventional heating as well as microwave irradiations method followed by complexation with Cu(II) metal. The synthesized compounds have been characterised by elemental analysis, melting point determination, FTIR, UV-visible spectral analysis. Thiosemicarbazone ligands behave as bidentate ligand and forms octahedral complexes with Cu(II). The synthesized ligands and their new metal complexes have been screened in vitro for antibacterial activity against Escherichia coli, Staphylococcus aureus and Bacillus subtilis bacteria. The result shows that all the Cu(II) complexes are potent antibacterial agents against these bacteria.
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