Xue Wen, Li Ziyong, Liu Guoxing, Chen Xiaoqiang, Li Tingting, Liu Sheng Hua, Yin Jun
Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, PR China.
Org Biomol Chem. 2014 Jul 21;12(27):4862-71. doi: 10.1039/c4ob00602j.
The construction of novel mechanically interlocked structures has become a topic of great current interest due to the requirements of topology and their potential application in molecular machines and devices. Rotaxane and catenane as two basic topological frameworks can be used to construct the fused structures. In the current investigation, a class of novel ammonium backbones were synthesized. The ammonium group incorporated in the linear part of the molecule can be used for templating rotaxane formation while the macrocyclic part of the molecule can be used for templating catenane formation. Accordingly, they were subjected to dynamic covalent chemistry, resulting in a series of [n]rota[n]catenane structures (n = 2, 3, 4). In this process, the N-hetero crown ethers were installed on ammonium template sites of linear and macrocyclic components all at once by a template-directed clipping reaction. The results showed that these novel building blocks could be assembled with high efficiencies. Finally, this investigation provides a foundation for future studies aimed at constructing complicated integrated structures or polymers with multiple topological units.
由于拓扑结构的要求及其在分子机器和器件中的潜在应用,新型机械互锁结构的构建已成为当前备受关注的话题。轮烷和索烃作为两种基本的拓扑框架可用于构建融合结构。在当前的研究中,合成了一类新型铵基主链。分子线性部分所含的铵基团可用于模板化轮烷的形成,而分子的大环部分可用于模板化索烃的形成。因此,它们经历了动态共价化学过程,得到了一系列的[n]轮[n]索烃结构(n = 2、3、4)。在此过程中,通过模板导向的剪切反应,将N-杂冠醚一次性安装在线性和大环组分的铵模板位点上。结果表明,这些新型构建块能够高效组装。最后,该研究为未来旨在构建具有多个拓扑单元的复杂集成结构或聚合物的研究奠定了基础。