Dynamic Covalent Self-Assembly Based on Oxime Condensation

被引:38
作者
Shen, Libo [1 ]
Cao, Ning [1 ]
Tong, Lu [1 ]
Zhang, Xinjiang [1 ]
Wu, Guangcheng [1 ]
Jiao, Tianyu [1 ]
Yin, Qi [1 ]
Zhu, Jiaqi [1 ]
Pan, Yuanjiang [1 ]
Li, Hao [1 ]
机构
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
catenanes; dynamic covalent bonds; oxime; self-assembly; Supramolecular chemistry; ORGANIC CAGE; ONE-POT; SURFACE; HYDRAZONES; DISULFIDE; EXCHANGE; CATENANE;
D O I
10.1002/anie.201811025
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxime, whose dynamic nature was reported to be switchable between ON/OFF by tuning the acidity, is employed in a novel type of dynamic covalent approach that is amenable to use in water for self-assembly of purely organic molecules with complex topology. In strongly acidic conditions, the dynamic nature of oxime is turned ON, allowing occurrence of error-checking and therefore a catenane and a macrocycle self-assembled in high yields. In neutral conditions, oxime ceases to be dynamic, which helps to trap the self-assembled products even when the driving forces of their formation are removed. We envision that this switchable behaviour might help, at least partially, to resolve a commonly encountered drawback of dynamic covalent chemistry, namely that the intrinsic stability of the self-assembled products containing dynamic bonds, such as imine or hydrazone, are often jeopardized by their reversible nature.
引用
收藏
页码:16486 / 16490
页数:5
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