A Self-Assembled Cage Binding Iodide Anions over Other Halide Ions in Water

被引:31
|
作者
Wu, Yating [1 ]
Zhang, Chi [1 ]
Fang, Shuai [1 ]
Zhu, Dingsheng [1 ]
Chen, Yixin [1 ]
Ge, Chenqi [1 ]
Tang, Hua [1 ]
Li, Hao [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Peoples R China
[2] Zhejiang Univ, ZJU Hangzhou Global Sci & Technol Innovat Ctr, Hangzhou 311215, Peoples R China
基金
中国国家自然科学基金;
关键词
Dynamic Covalent Chemistry; Host-Guest Systems; Molecular Recognition; Organic Cages; Supramolecular Chemistry; RECOGNITION; BOND; MACROCYCLE; BAMBUSURIL; DONORS;
D O I
10.1002/anie.202209078
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A triangular-prism shaped cage was self-assembled by the formation of a dynamic covalent bond, namely a hydrazone, in acidic aqueous solution. The hexacationic host bears a number of relatively acidic protons pointing inside the cage cavity, which is able to accommodate an iodide anion selectively in water over other halide anions such as F-, Cl-, and Br-, which are more hydrated. As a comparison, a macrocycle analogue bearing fewer positive charges and fewer hydrogen bond donors shows no anion binding ability. As inferred from the single-crystal structure and theoretical calculations, the ability of the cage to selectively recognize iodide anions results from the combination of electrostatic forces, C-H center dot center dot center dot I- hydrogen bonds, and the hydrophobic effect.
引用
收藏
页数:6
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