Department of Chemistry, Yasouj University, Yasouj 75918-74831, Iran.
Department of Chemistry, Yasouj University, Yasouj 75918-74831, Iran.
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Aug 14;129:382-91. doi: 10.1016/j.saa.2014.03.085. Epub 2014 Apr 1.
Some novel nano-sized structure zinc complexes of a new Schiff base ligand entitled as (3-nitro-benzylidene)-{2-[2-(3-nitro-phenyl)-imidazolidine-1-yl]-ethyl}-amine(L) with general formula of ZnLX2 wherein X=Cl(-), Br(-), I(-), SCN(-) and N3(-) have been synthesized under ultrasonic conditions. The ligand and its complexes have been characterized by elemental analysis, molar conductance measurements, FT-IR, (1)H and (13)C NMR and UV-Visible spectroscopy. The resulting data from spectral investigation especially (1)H and (13)C NMR well confirmed formation of an imidazolidine ring in the ligand structure. Transmission electron microscopy (TEM) showed nano-size structures with average particle sizes of 21.80-78.10nm for the zinc(II) Schiff base complexes. The free Schiff base and its Zn(II) complexes have been screened in vitro both for antibacterial activity against some gram-positive and gram-negative bacteria and also for antifungal activity. The metal complexes were found to be more active than the free Schiff base ligand. The results showed that ZnL(N3)2 is the most effective inhibitor against Escherichia coli, Pseudomonas aereuguinosa, Staphylococcus aureus and Candida albicans while ZnLBr2 was found to be more effective against Bacillus subtillis than other compounds. Moreover, DNA cleavage potential of all compounds with plasmid DNA was investigated. The results showed that the ligand and ZnLCl2 complex cleave DNA more efficiently than others. In final, thermal analysis of ligand and its complexes revealed that they are decomposed via 2-3 thermal steps in the range of room temperature to 1000°C. Furthermore some activation kinetic parameters such as A, E(), ΔH(), ΔS() and ΔG() were calculated based on TG/DTA plots by use of coats - Redfern relation. Positive values of activation energy evaluated for the compounds confirmed the thermal stability of them. In addition to, the positive ΔH(), and ΔG() values suggested endothermic character for the thermal decomposition steps.
一些新型纳米结构锌配合物的新型希夫碱配体命名为(3-硝基苄叉基)- {2-[2-(3-硝基苯基)-咪唑烷-1-基]乙基} -胺(L)与一般式ZnLX2 其中 X = Cl(-),Br(-),I(-),SCN(-)和N3(-)已在超声条件下合成。配体及其配合物通过元素分析,摩尔电导率测量,FT-IR,(1)H和(13)C NMR 和 UV-Visible 光谱进行表征。光谱研究特别是(1)H 和(13)C NMR 的结果数据很好地证实了配体结构中环咪唑烷的形成。透射电子显微镜(TEM)显示锌(II)希夫碱配合物的纳米尺寸结构,平均粒径为 21.80-78.10nm。游离希夫碱及其锌(II)配合物均对一些革兰氏阳性和革兰氏阴性细菌进行了体外抗菌活性筛选,同时也进行了抗真菌活性筛选。金属配合物的活性高于游离希夫碱配体。结果表明,ZnL(N3)2 是对大肠杆菌,铜绿假单胞菌,金黄色葡萄球菌和白色念珠菌最有效的抑制剂,而 ZnLBr2 对枯草芽孢杆菌的抑制作用比其他化合物更有效。此外,还研究了所有化合物与质粒 DNA 的 DNA 断裂潜力。结果表明,配体和 ZnLCl2 配合物比其他化合物更有效地切割 DNA。最后,配体及其配合物的热分析表明,它们在室温至 1000°C 的范围内通过 2-3 个热步骤分解。此外,根据 TG/DTA 图谱,通过使用 coats - Redfern 关系计算了一些活化动力学参数,如 A,E(),ΔH(),ΔS()和ΔG()。评估化合物的活化能正值证实了它们的热稳定性。此外,正的ΔH()和ΔG()值表明热分解步骤为吸热特征。