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Convenient synthesis and anion recognition property of acylhydrazone-based molecular tweezer receptors

机译:基于酰基hydr的分子镊子受体的便捷合成和阴离子识别特性

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摘要

Three acylhydrazone-based compounds were designed as novel neutral sensors for anions, and synthesized by simple steps in good yields. Their anion recognition properties were studied by UV-vis and ~1H-NMR spectroscopy. The results showed that the receptors 1, 2, and 3 all had a better selectivity for F~-and CH3COO~-, but no evident binding with Cl~-, Br~-, I~-, NO_3~-, H2PO_4~-, or HSO_4~-. The results indicated that anion recognition was achieved via convergent hydrogen bond interactions from acylhydrazone functionality on the side arms. The UV-vis data indicated that a 1:1 stoichiometry complex was formed between compounds 1, 2, or 3 and anions. The binding and selectivity were also tuned by the change of the place of the nitro group attached to the phenyl. Moreover, receptor 3 can act as the colorimetric sensor for such anions as F~- and CH3COO~- , and the recognition mechanism and binding mode were discussed.
机译:三种基于酰基hydr的化合物被设计为新型的阴离子中性传感器,并通过简单的步骤以高收率合成。通过紫外可见光谱和〜1H-NMR光谱研究了它们的阴离子识别特性。结果表明,受体1、2和3对F〜-和CH3COO〜-均具有较好的选择性,但与Cl〜-,Br〜-,I〜-,NO_3〜-,H2PO_4〜-没有明显的结合。或HSO_4〜-。结果表明,阴离子的识别是通过侧hydr上酰基hydr官能团的汇聚氢键相互作用实现的。紫外可见数据表明,化合物1、2或3与阴离子之间形成了1:1的化学计量配合物。结合和选择性也通过连接在苯基上的硝基位置的变化来调节。此外,受体3可以作为F〜-和CH3COO〜-等阴离子的比色传感器,并讨论了其识别机理和结合方式。

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