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Synthesis, characterisation, in vitro antimicrobial, antioxidant and anti-inflammatory activities of diorganotin(IV) complexes derived from salicylaldehyde Schiff bases

机译:衍生自水杨醛席夫基地的二氧化素(IV)复合物的合成,表征,体外抗微生物,抗氧化剂和抗炎活性

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摘要

A new series of diorganotin(IV) complexes of 4-((2-hydroxybenzylidene)amino)-[1,1-biphenyl]-3-ol (H2L1), 4-((2-hydroxy-5-nitrobenzylidene)amino)-[1,1-biphenyl]-3-ol (H2L2), 4-((3-bromo-2-hydroxy-5-nitrobenzylidene)amino)-[1,1-biphenyl]-3-ol (H2L3) and 4-((3,5-dibromo-2-hydroxybenzylidene)amino)-[1,1-biphenyl]-3-ol (H2L4) Schiff base ligands with general formula R2SnL (where R=Me, Et, Bu and Ph) were synthesized. Structural aspect of these synthesized compounds have been described with the help of elemental analysis and spectroscopic techniques like FT-IR, UV-Vis, NMR, Mass and fluorescence. Schiff bases coordinated to tin metal as dibasic tridentate ligand through imine nitrogen and two phenolic oxygen atoms forming pentacoordinated complexes. Metal complexes gave low molar conductance value describing their non-electrolytic nature. Thermal decomposition of the complexes resulted in the formation of SnO2 as end product. The in vitro antimicrobial activities have been evaluated against Gram positive bacteria, Gram-negative bacteria and two fungal strains. The screening evaluation showed that organotin(IV) complexes have better antimicrobial activity. The free radical scavenging ability of the compounds was invest by in vitro antioxidant assay involving DPPH radical and was found to be moderately good. The anti-inflammatory activity was done by egg albumin method and percentage inhibition of protein denaturation was calculated. By comparing the biological activities of the synthesized compounds it was found that metal complexes were more potent than the free ligands and compounds 16, 20 were having more potential as drugs.
机译:4 - ((2-羟基苄基)氨基) - [1,1-联苯基] -3-醇(H2L1),4-((2-羟基-5-硝基苄基)氨基)的新系列复合物 - [1,1-联苯基] -3-醇(H2L2),4 - ((3-溴-2-羟基-5-硝基苄基)氨基) - [1,1-联苯基] -3-醇(H2L3)和4 - ((3,5-二溴-2-羟基苄基二亚苄基)氨基) - [1,1-联苯] -3-醇(H2L4)席夫碱配体,具有通式R2SN1(其中R = ME,ET,BU和PH)被合成了。已经借助于元素分析和光谱技术描述了这些合成化合物的结构方面,例如FT-IR,UV-Vis,NMR,质量和荧光。通过亚胺氮和两种形成五烯氧原子,与锡金属配位与锡金属配位,通过亚胺氮和两种酚类氧原子形成五苯甲酸盐。金属配合物给出了描述其非电解性质的低摩尔电导值。复合物的热分解导致SnO2作为最终产品的形成。已经评估了体外抗微生物活性对革兰氏阳性细菌,革兰氏阴性细菌和两种真菌菌株进行了评估。筛选评估显示有机锡(IV)配合物具有更好的抗微生物活性。化合物的自由基清除能力通过涉及DPPH基团的体外抗氧化剂测定来投资,并发现是适度的。通过蛋白法进行抗炎活性,并计算蛋白质变性的抑制百分比。通过比较合成化合物的生物活性,发现金属配合物比游离配体和化合物16,20具有更高的药物作为药物。

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