Binding of Carbonated Anions to Cationic Hexaureachromium(III): Synthesis, Characterization and Antimicrobial Activity of [Cr(CO(NH2 )2 )6 ](HCO3 )3 and [Cr(CO(NH2 )2 )6 ]2 (CO3 )3

IF 0.4 Q4 PHARMACOLOGY & PHARMACY
V. Prakash
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引用次数: 0

Abstract

Aim: The aim of the study is to synthesize two new hexaureachromium complexes: [Cr(CO(NH2 ) 2 ) 6 ](HCO3 ) 3 (1), [Cr(CO(NH2 ) 2 ) 6 ] 2 (CO3 ) 3 (2) followed by the analysis of binding ability of hexaureachromium(III) cation towards carbonated anions ( 2 HCO and CO 3 3 − − ) and their antimicrobial activities against Escherichia coli, Staphylococcus aureus S. aurses (for anti-bacterial), and Aspergillus niger (for anti-fungal). Materials and Methods: The synthesized compounds 1 and 2 were characterized by spectroscopic studies (fourier-transform infrared and ultraviolet [UV]- visible). The binding properties of [Cr(CO(NH2 ) 2 ) 6 ] 3+ ([HuCr]3+) with carbonated anions ( 2 HCO and CO 3 3 − − ) in aqueous medium have been determined with standard UV–visible spectrophotometerthrough titration method. Further, the stoichiometric ratios for complexes 1 and 2 were found through Job’s plot. All compounds were also tested for antimicrobial activity against selected strains. Results and Discussion: The cation, [HuCr]3+, contains ligand urea bearing H-bond donors which are capable of forming hydrogen bonds. The binding constant values obtained are found to be 10.5334 for and 15.7377 for . Further, the stoichiometric ratios for complexes 1 and 2 have been found to be 1:3 and 2:3, respectively. [HuCr]Cl3 , 1 and 2 show the maximum zone of inhibition at 200 μg/mL but the starting material [HuCr]Cl3 and compound 1 does not show any activity against A. niger at 50 and 100 μg/mL concentration. Conclusion: The ionic reactions between anion receptor [HuCr]3+ and carbonated anions in aqueous solution have been investigated and characterized by spectroscopic (infrared and UV–visible) techniques. The results obtained indicate that the binding ability of the cation [HuCr]3+ towards carbonated anions is in the order 2 CO3 − > HCO3 − . Thus, the selectivity of receptors for particular anion can be chosen. The results predict that the octahedral geometry of [HuCr]3+ is capable enough to target both the carbonated anions. [HuCr]Cl3 and compound 1 do not show any activity against A. niger at 50 and 100 μg/mL concentration while compound 2 is found to be potent against all the tested organisms (E. coli, S. aurses, and A. niger).
[Cr(CO(NH2)2)6](HCO3)3和[Cr(CO(NH2)2)6]2 (CO3)3的合成、表征及抗菌活性
目的:合成两种新的六脲铬配合物:[Cr(CO(NH2)2)6](HCO3)3(1)、[Cr(CO(NH2,2)6]2(CO3)3(2),和黑曲霉(用于抗真菌)。材料与方法:通过红外光谱和紫外可见光谱对合成的化合物1和2进行了表征。用标准紫外-可见分光光度计通过滴定法测定了[Cr(CO(NH2)2)6]3+([HuCr]3+)与碳酸化阴离子(2 HCO和CO 3−−)在水介质中的结合性能。此外,配合物1和2的化学计量比通过Job's图得到。还测试了所有化合物对选定菌株的抗微生物活性。结果与讨论:阳离子[HuCr]3+含有能够形成氢键的带有氢键供体的配体脲。得到的结合常数值为10.5334和15.7377。此外,已经发现配合物1和2的化学计量比分别为1:3和2:3。[HuCr]Cl3、1和2在200μg/mL时显示出最大抑制区,但起始材料[HuCr]Cl3和化合物1在50和100μg/mL浓度下对黑曲霉没有显示出任何活性。结论:阴离子受体[HuCr]3+与水溶液中碳酸化阴离子之间的离子反应已通过光谱(红外和紫外-可见光)技术进行了研究和表征。结果表明,阳离子[HuCr]3+对碳酸化阴离子的结合能力为2CO3−>HCO3−。因此,可以选择受体对特定阴离子的选择性。结果预测,[HuCr]3+的八面体几何结构足以靶向两种碳酸化阴离子。[HuCr]Cl3和化合物1在50和100μg/mL浓度下对黑曲霉没有任何活性,而化合物2被发现对所有测试的生物体(大肠杆菌、金黄色葡萄球菌和黑曲霉)都有效。
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来源期刊
Asian Journal of  Pharmaceutics
Asian Journal of Pharmaceutics PHARMACOLOGY & PHARMACY-
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0.00%
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47
期刊介绍: Character of the publications: -Pharmaceutics and Pharmaceutical Technology -Formulation Design and Development -Drug Discovery and Development Interface -Manufacturing Science and Engineering -Pharmacokinetics, Pharmacodynamics, and Drug Metabolism -Clinical Pharmacology, General Medicine and Translational Research -Physical Pharmacy and Biopharmaceutics -Novel Drug delivery system -Biotechnology & Microbiological evaluations -Regulatory Sciences
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