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Selective recognition of sulfate ions by tripodal cyclic peptides functionalised with (thio)urea binding sites

机译:通过具有(硫)脲结合位点功能化的三脚架环肽选择性识别硫酸根离子

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摘要

A tripodal urea and tripodal thiourea with the same cyclic peptide core have been synthesised and their anion binding ability investigated. In CDCl_3, the tripodal urea self-associates whereas the thiourea does not. Neither compound shows self-association in the more polar 10% v/v DMSO-d_6/CDCl_3. Both compounds bind strongly and selectively to sulfate ions in CDCl_3 and 10% v/v DMSO-d_6/CDCl_3. This selectivity is attributed to a unique binding mode for sulfate, in which this tetrahedral anion forms nine hydrogen bonds to the receptors, with three of these coming from the amide protons of the cyclic peptide.
机译:合成了具有相同环肽核心的三脚架尿素和三脚架硫脲,并研究了它们的阴离子结合能力。在CDCl_3中,三脚架尿素会自缔合,而硫脲则不会。两种化合物在极性更高的10%v / v DMSO-d_6 / CDCl_3中均未显示出自缔合。两种化合物均与CDCl_3和10%v / v DMSO-d_6 / CDCl_3中的硫酸根离子牢固且选择性地结合。该选择性归因于硫酸盐的独特结合方式,其中该四面体阴离子与受体形成九个氢键,其中三个来自环肽的酰胺质子。

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  • 来源
    《Organic & biomolecular chemistry》 |2012年第13期|p.2664-2672|共9页
  • 作者单位

    School of Chemistry (F11), The University of Sydney, 2006 NSW,Australia;

    School of Chemistry (F11), The University of Sydney, 2006 NSW,Australia;

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