Waelès P, Clavel C, Fournel-Marotte K, Coutrot F
Supramolecular Machines and Architectures Team , Faculté des Sciences , Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS , Université Montpellier , ENSCM , case courrier 1706, Bâtiment Chimie (17), 3ème étage, Place Eugène Bataillon , 34095 Montpellier cedex 5 , France . Email:
Chem Sci. 2015 Aug 1;6(8):4828-4836. doi: 10.1039/c5sc01722j. Epub 2015 Jun 2.
We report a diverted route to [1]rotaxane and tris-branched [1]rotaxane that are devoid of any efficient template and which could not be obtained by classical straightforward strategies. The described chemical route relies on the utilization of a "macrocycle transporter", which is able first to bind a macrocycle, second to link temporarily a triazolium-containing molecular axle, and third to deliver the macrocycle around the new docked axle through molecular machinery in a [1]rotaxane structure. The extended encircled thread is eventually cleaved by an amine or a triamine to afford the triazolium-containing [1]rotaxanes, releasing at the same time, the macrocycle transporter as a recyclable species.
我们报道了一种制备[1]轮烷和三分支[1]轮烷的迂回路线,该路线无需任何有效的模板,且无法通过传统的直接策略获得。所描述的化学路线依赖于“大环转运体”的利用,它首先能够结合一个大环,其次能够暂时连接一个含三唑鎓的分子轴,第三能够通过分子机制将大环围绕新对接的轴传递形成[1]轮烷结构。最终,延伸的环状链被胺或三胺切断,得到含三唑鎓的[1]轮烷,同时释放出可循环利用的大环转运体。