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Synthesis, characterization and neurotoxicity of multidentate azomethine series and their Cu(II) and Ni(II) Complexes

机译:多齿偶氮甲碱系列及其Cu(II)和Ni(II)配合物的合成,表征和神经毒性

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Two novel azomethine ligands L1 and L2 are synthesized from guanidine where L1 is (1E,3E)-1,3-bis(2,4-dihydroxybenzylidene)guanidine and L2 is (1E,3E)-1,3-bis(1-(2,4-dihydroxyphenyl)ethylidene)guanidine. The ligands are reacted with Cu(II) and Ni(II) to produce complexes CuL1, CuL2, NiL1 and NiL2. All the compounds are characterized by Fourier Transform Infrared (FTIR) spectroscopy, CHN elemental analysis, Proton Nuclear Magnetic Resonance spectroscopy and magnetic susceptibility measurements. The shift of ν(C=N) peaks upon complexation indicates that the azomethine nitrogens are involved in the chelation to the metal centres. The magnetic susceptibility measurements show that copper(II) complexes are paramagnetic with 1 unpaired electron while nickel(II) complexes are diamagnetic. An investigation for neurotoxicity against treated neuroblastoma SH-SY5Y cell lines showed non-toxic effect for the range of concentrations investigated.
机译:由胍合成两个新颖的偶氮甲碱配体L1和L2,其中L1为(1E,3E)-1,3-双(2,4-二羟基亚苄基)胍,L2为(1E,3E)-1,3-bis(1- (2,4-二羟基苯基)亚乙基)胍。配体与Cu(II)和Ni(II)反应生成配合物CuL1,CuL2,NiL1和NiL2。所有化合物均通过傅里叶变换红外(FTIR)光谱,CHN元素分析,质子核磁共振光谱和磁化率测量进行表征。络合时ν(C = N)峰的移动表明,甲亚胺氮原子参与了与金属中心的螯合。磁化率测量表明,铜(II)配合物是顺磁性的,带有1个未配对的电子,而镍(II)配合物是抗磁性的。针对治疗的成神经细胞瘤SH-SY5Y细胞系的神经毒性研究表明,在所研究的浓度范围内,无毒作用。

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