首页> 外文期刊>The Journal of Organic Chemistry >Solution-State Anion Recognition, and Structural Studies, of a Series of Electron-Rich meta-Phenylene Bis(phenylurea) Receptors and Their Self-Assembled Structures
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Solution-State Anion Recognition, and Structural Studies, of a Series of Electron-Rich meta-Phenylene Bis(phenylurea) Receptors and Their Self-Assembled Structures

机译:解决方案 - 状态阴离子识别和结构研究,其富含电子富含电子的亚苯基双(苯脲)受体及其自组装结构

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摘要

meta-Phenylene bis(phenylurea) receptors 1-4 were designed and synthesized to investigate the association between receptor shape, anion-selective binding and aniondirected self-assembly processes. Solution studies, performed through H-1 NMR titrations with a variety of tetra-N-butylammonium salts, demonstrated strong binding of 2 equiv of H2PO4-, AcO-, BzO(-) anions and comparatively weak binding of Cl-, HSO4-, and SO42- anions. Binding modes and stability constants (log beta) were determined by regression analysis of the obtained H-1 NMR titration data in DMSO-d(6), and the cooperativities of the binding interactions were probed. Host-guest complexes of receptors 1 and 2 were studied in the crystalline phase to further probe the anion-binding behavior of this motif. This included a triple-stranded helicate consisting of three strands of receptor 2 arranged around a mixed-phosphate anionic core, which was characterized by using X-ray crystallography.
机译:设计和合成了亚苯基双(苯脲)受体1-4,以研究受体形状,阴离子选择性结合和阴离子一致的自组装方法之间的关联。 通过H-1 NMR滴定进行的解决方案研究与各种四丁基铵盐进行,表现出强烈的2当量的H2PO4-,ACO-,BZO( - )阴离子的结合,并且Cl-,HSO4-的相对较弱的结合, 和SO42-阴离子。 通过在DMSO-D(6)中获得的H-1 NMR滴定数据的回归分析确定结合模式和稳定性常数(LOGβ),并探测结合相互作用的合作。 在结晶期中研究了受体1和2的宿主 - 客体复合物,以进一步探测该基序的阴离子结合行为。 这包括三链螺旋,其由围绕混合磷酸阴离子核心布置的三股受体2,其特征在于使用X射线晶体学。

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