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A Halogen-Bonding Bis-triazolium Rotaxane for Halide-Selective Anion Recognition

机译:卤素键联双三唑烷轮烷用于卤化物选择性阴离子的识别

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摘要

A systematic study on the anion-binding properties of acyclic halogen-and hydrogen-bonding bis-triazolium carbazole receptors is described. The halide-binding potency of halogen-bonding bis-iodotriazolium carbazole receptors was found to be far superior to their hydrogen-bonding bis-triazolium-based analogues. This led to the synthesis of a mixed halogen-and hydrogen-bonding rotaxane host containing a bis-iodotriazolium carbazole axle component. The rotaxane's anion recognition properties, determined by H-1 NMR titration experiments in a competitive aqueous solvent mixture, demonstrated the preorganised halogen-bonding interlocked host cavity to be halide-selective, with a strong binding affinity for bromide.
机译:对无环卤素和氢键合的双三唑鎓咔唑受体的阴离子结合性质进行了系统的研究。发现卤素键合的双碘三唑鎓咔唑受体的卤化物结合效能远远优于其氢键合的双三唑鎓类似物。这导致了含有双碘三唑鎓咔唑轴组分的卤素键和氢键混合轮烷的主体的合成。通过在竞争性水性溶剂混合物中进行H-1 NMR滴定实验确定的轮烷的阴离子识别特性表明,预先组织好的卤素键联锁主体腔具有卤化物选择性,对溴化物具有很强的结合亲和力。

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