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New Microbe Killers: Self-Assembled Silver(I) Coordination Polymers Driven by a Cagelike Aminophosphine

机译:新的杀微生物剂:笼状氨基膦驱动的自组装银(I)配位聚合物

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摘要

New Ag(I) coordination polymers, formulated as [Ag( -PTAH)(NO ) ] ( ) and [Ag( -PTA)(NO )] ( ), were self-assembled as light- and air-stable microcrystalline solids and fully characterized by NMR and IR spectroscopy, electrospray ionization mass spectrometry (ESI-MS(±), elemental analysis, powder (PXRD) and single-crystal X-ray diffraction. Their crystal structures reveal resembling 1D metal-ligand chains that are driven by the 1,3,5-triaza-7-phospaadamantane (PTA) linkers and supported by terminal nitrate or nitrite ligands; these chains were classified within a topological type. Additionally, the structure of features a 1D→2D network extension through intermolecular hydrogen bonds, forming a two-dimensional hydrogen-bonded network with topology. Furthermore, both products and exhibit remarkable antimicrobial activity against different human pathogen bacteria ( , , ) and yeast ( ), which is significantly superior to the activity of silver(I) nitrate as a reference topical antimicrobial.
机译:配制为[Ag(-PTAH)(NO)]()和[Ag(-PTA)(NO)]()的新型Ag(I)配位聚合物可自组装为光和空气稳定的微晶固体,并通过NMR和IR光谱,电喷雾电离质谱(ESI-MS(±),元素分析,粉末(PXRD)和单晶X射线衍射)进行完全表征,它们的晶体结构揭示了类似的一维金属-配体链,这些链由1,3,5-triaza-7-phospaadamantane(PTA)接头,并由末端硝酸盐或亚硝酸盐配体支撑;这些链被分类为拓扑类型;另外,其结构特征是通过分子间氢键实现1D→2D网络扩展,形成了具有拓扑结构的二维氢键网络,而且,这两种产品对不同的人类病原体细菌(,,)和酵母菌()均显示出显着的抗菌活性,明显优于硝酸银(I)的活性。参考主题l抗菌药。

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