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高水溶性双脲衍生物的阴离子识别。

Highly soluble bisurea derivatives for anion recognition.

机构信息

Department of Chemistry, Faculty of Science, Yamagata University, Yamagata 990-8560, Japan.

Institute for Advanced Integrated Technology, Resonac Co., 48 Wadai, Tsukuba, Ibaraki, 300-4247, Japan.

出版信息

Org Biomol Chem. 2023 Jun 28;21(25):5281-5287. doi: 10.1039/d3ob00802a.

Abstract

Highly soluble bisurea derivatives having 1,2-phenoxyethane (receptors 2) and 1,2-ethoxyethane (3) moieties as spacer groups were designed and prepared based on previously reported receptors with the 2,2'-binaphthyl group as a spacer (1). The receptors can be prepared in fewer steps from commercially available starting materials. The solubilities and anion recognition abilities were evaluated by UV-vis and NMR spectral methods. Receptors 2 and 3 bearing a flexible linker showed good solubilities in common organic solvents such as CHCl, MeCN, 2-butanone, toluene, and THF. Although the anion recognition abilities of receptors 2 and 3 were lower than those of receptors 1, the greatly improved solubilities of receptors 2 and 3 allow the association of anions under more concentrated conditions for the solubilisation of salts such as lithium chloride in organic solvents.

摘要

高水溶性的双脒衍生物具有 1,2-苯氧基乙烷(受体 2)和 1,2-乙氧基乙烷(3)部分作为间隔基,基于之前报道的带有 2,2'-联萘基作为间隔基的受体(1)设计和制备。受体可以从商业上可获得的起始材料通过更少的步骤制备。通过 UV-vis 和 NMR 光谱方法评估了受体的溶解度和阴离子识别能力。带有柔性连接基团的受体 2 和 3 在常见有机溶剂如 CHCl、MeCN、2-丁酮、甲苯和 THF 中具有良好的溶解度。尽管受体 2 和 3 的阴离子识别能力低于受体 1,但受体 2 和 3 的溶解度大大提高,允许在更浓的条件下与阴离子缔合,以溶解盐,如氯化锂在有机溶剂中。

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