Department of Chemistry, National University of Ireland Maynooth, Maynooth, Ireland.
Synthesis and Solid State Pharmaceutical Centre (SSPC), Ireland.
Org Biomol Chem. 2022 Sep 14;20(35):7056-7066. doi: 10.1039/d2ob01176j.
Stimuli responsive anion transport is becoming an important aspect of supramolecular anion recognition chemistry. Herein, we report the synthesis of a family of anion receptors that incorporate a new anion binding motif, amidosquaramides. We show using experimental and computational methods that these receptors have p values close to physiological pH but also display intramolecular H-bonding interactions that affect anion recognition. Moreover, moderate activity in a Cl/NO exchange assay is observed at physiological pH that can be effectively 'switched on' when repeated under acidic conditions. The reported findings provide synthetic methods that can be used for the construction of more complex squaramide based anion receptors and also provide insight into the importance of conformational analysis when considering receptor design.
刺激响应型阴离子传输正在成为超分子阴离子识别化学的一个重要方面。在此,我们报告了一类阴离子受体的合成,其中包含了一种新的阴离子结合基序,酰胺基-squaramide。我们通过实验和计算方法表明,这些受体的 p 值接近生理 pH 值,但也显示出影响阴离子识别的分子内氢键相互作用。此外,在生理 pH 值下观察到在 Cl/NO 交换测定中具有中等活性,并且在重复酸性条件下可以有效地“开启”。所报道的发现提供了可用于构建更复杂的基于 squaramide 的阴离子受体的合成方法,并为考虑受体设计时构象分析的重要性提供了见解。