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首页> 外文期刊>ACS Omega >4-Sulfocalix[4]arene/Cucurbit[7]uril-Based Supramolecular Assemblies through the Outer Surface Interactions of Cucurbit[n]uril
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4-Sulfocalix[4]arene/Cucurbit[7]uril-Based Supramolecular Assemblies through the Outer Surface Interactions of Cucurbit[n]uril

机译:通过葫芦丝[ n ]尿嘧啶的外表面相互作用作用于4-Sulfocalix [4]芳烃/葫芦[7]尿素的超分子组装

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Upon mixing of aqueous solutions of the freely soluble building blocks cucurbit[7]uril (Q[7]) and 4-sulfocalix[4]arene (SC[4]A), white microcrystals instantly separate in near-quantitative yield. The driving force for this assembly is suggested to be the outer-surface interaction of the Q[n ]. Dynamic light scattering, scanning electron microscopy, and NMR (diffusion-ordered NMR spectroscopy) analyses have confirmed the supramolecular aggregation of Q[7] and SC[4]A. Titration ~(1)H NMR spectroscopy and isothermal titration calorimetry have shown that the interaction ratio of Q[7] and SC[4]A is close to 3:1. Moreover, the Q[7]/SC[4]A-based supramolecular assembly can accommodate molecules of some volatile compounds or luminescent dyes. Thus, this work offers a simple and highly efficient means of preparing adsorbent or solid fluorescent materials.
机译:当将易溶于水的葫芦[7]尿素(Q [7])和4-磺胺基[4]芳烃(SC [4] A)的水溶液混合后,白色微晶立即以接近定量的产率分离。建议该组件的驱动力是Q [n]的外表面相互作用。动态光散射,扫描电子显微镜和NMR(扩散有序NMR光谱)分析已确认Q [7]和SC [4] A的超分子聚集。滴定〜(1)H NMR光谱和等温滴定热法表明,Q [7]和SC [4] A的相互作用比接近3:1。此外,基于Q [7] / SC [4] A的超分子组件可以容纳某些挥发性化合物或发光染料的分子。因此,这项工作为制备吸附剂或固体荧光材料提供了一种简单而高效的方法。

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