| Literature DB >> 30334325 |
Libo Shen1, Ning Cao1, Lu Tong1, Xinjiang Zhang1, Guangcheng Wu1, Tianyu Jiao1, Qi Yin1, Jiaqi Zhu1, Yuanjiang Pan1, Hao Li1.
Abstract
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.Entities:
Keywords: Supramolecular chemistry; catenanes; dynamic covalent bonds; oxime; self-assembly
Year: 2018 PMID: 30334325 DOI: 10.1002/anie.201811025
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336