首页> 外文期刊>Journal of Organometallic Chemistry >Benzoxazole and dioxolane substituted benzimidazole-based N-heterocyclic carbene-silver( I) complexes: Synthesis, structural characterization and in vitro antimicrobial activity
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Benzoxazole and dioxolane substituted benzimidazole-based N-heterocyclic carbene-silver( I) complexes: Synthesis, structural characterization and in vitro antimicrobial activity

机译:苯并恶唑和二氧戊烷取代的苯并咪唑基N-杂环碳甲烷 - 银(I)配合物:合成,结构表征和体外抗菌活性

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摘要

A novel series of 1,3-benzoxazole and 1,3-dioxolane substituted benzimidazole-based N-heterocyclic carbene (NHC) precursors (6a-b and 11a-b) and their corresponding NHC-silver(I) acetate (12a-b and 14a-b) and bis-NHC-silver(I) hexafluorophosphate complexes (13a-b and 15a-b) were synthesized and characterized by H-1 NMR, C-13 NMR, ATR-IR spectroscopic methods and elemental analysis techniques. Also, the molecular structure of benzimidazolium salt (6a) and bis-NHC-silver(I) hexafluorophosphate complex (13b) were unambiguously established by single crystal X-ray diffraction analysis. Fascinatingly, bis-NHC-silver(I) hexafluorophosphate complex (13b) was revealed to be dinuclear in nature. All the azolium salts (6a-b and 11a-b) as well as the corresponding silver(I) complexes (12a-b, 13a-b, 14a-b and 15a-b) were evaluated for their antimicrobial potential against Gram positive (Staphylococcus aureus), and a set of Gram negative (Escherichia coli, Klebsiella pneumoniae, Acinetobacter baumannii and Pseudomonas aeruginosa) bacterial strains and two fungi, Candida albicans and Cryptococcus neoformans. Antimicrobial studies revealed the comparable activities of benzimidazolium salts (6a-b and 11a-b) and the silver(I) complexes (12a-b, 13a-b and 15a-b). Whereas, the 1,3-dioxolane substituted benzimidazole-based silver(I) acetate complexes (14a-b) demonstrated excellent potentials with both bacterial and fungal growth inhibition above 95%. (C) 2018 Elsevier B.V. All rights reserved.
机译:一种新的1,3-苯并恶唑和1,3-二氧戊烷取代的苯并咪唑基N-杂氮杂唑(NHC)前体(6A-B和11A-B)及其相应的NHC-银(I)乙酸酯(12A-B. 14A-B)和BIS-NHC-银(I)六氟磷酸盐配合物(13A-B和15A-B)被H-1 NMR,C-13 NMR,ATR-IR光谱方法和元素分析技术表征。而且,通过单晶X射线衍射分析明确地建立了苯并咪唑鎓盐(6A)和双-NHC-银(1)六氟磷酸盐复合物(13B)的分子结构。令人欣慰的是,BIS-NHC-银(I)六氟磷酸盐络合物(13b)在自然中是二维的。所有氮杂盐(6A-B和11A-B)以及相应的银(I)配合物(12A-B,13A-B,14A-B和15A-B)评价它们的抗微生物潜力(金黄色葡萄球菌,以及一套克阴性(大肠杆菌,Klebsiella pneumoniae,Acinetobacterbackia和Pseudomonas Aeruginosa)细菌菌株和两个真菌,念珠菌蛋白和碱性蛋白质。抗菌研究揭示了苯并咪唑盐(6a-b和11a-b)和银(I)配合物(12a-b,13a-b和15a-b)的可比活性。然而,1,3-二氧戊烷取代的苯并咪唑基银(I)乙酸盐配合物(14A-B)显示出优异的潜力,具有高于95%的细菌和真菌生长抑制。 (c)2018年elestvier b.v.保留所有权利。

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