Ong Whitney S Y, Smaldone Ronald A, Dodani Sheel C
Department of Chemistry and Biochemistry, The University of Texas at Dallas 800 West Campbell Road Richardson TX 75080 USA
Chem Sci. 2020 Jun 19;11(29):7716-7721. doi: 10.1039/d0sc02941f.
Neutral hosts for the recognition of anionic guests in water remain underdeveloped due to the inherent thermodynamic barrier for desolvation. To address this challenge, we have repurposed crosslinked porous organic polymers (POPs) as hosts. This polymer architecture affords a hydrophobic environment with a densely packed array of urea hydrogen bond donors to cooperatively promote anion desolvation and recognition in water. Using the principles of supramolecular design, we demonstrate through adsorption assays that the resulting Urea-POP-1 can recognize structurally different dyes containing phosphonate, sulfonate, and carboxylate anions in water. Moreover, when compared to Methyl-POP-1, a control POP lacking hydrogen bond donors, we find that the driving force for desolvation and adsorption of each dye is achieved through hydrophobic interactions with the POP backbone and, more importantly, cooperative hydrogen bonding interactions with the urea sidechains. This starting point sets the stage to exploit the modularity of our design to build a family of neutral polymer hosts with tunable pore sizes and anion preferences for fundamental investigations and targeted applications.
由于去溶剂化存在固有的热力学障碍,用于在水中识别阴离子客体的中性主体仍然发展不足。为应对这一挑战,我们将交联多孔有机聚合物(POPs)重新用作主体。这种聚合物结构提供了一个疏水环境,其中密集排列着尿素氢键供体,以协同促进水中阴离子的去溶剂化和识别。利用超分子设计原理,我们通过吸附试验证明,所得的尿素-POP-1能够识别水中含有膦酸根、磺酸根和羧酸根阴离子的结构不同的染料。此外,与缺乏氢键供体的对照POP甲基-POP-1相比,我们发现每种染料的去溶剂化和吸附驱动力是通过与POP主链的疏水相互作用实现的,更重要的是,通过与尿素侧链的协同氢键相互作用实现的。这一出发点为利用我们设计的模块化构建一系列具有可调孔径和阴离子偏好的中性聚合物主体奠定了基础,用于基础研究和靶向应用。