Supramolecular Machines and ARchitectures Team, Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS, UM1-UM2, Université Montpellier 2, Place Eugène Bataillon, case courrier 1706, Bât 17, 3ème étage, 34095 Montpellier Cedex 5 (France) http://www.glycorotaxane.fr.
Angew Chem Int Ed Engl. 2014 Jul 1;53(27):6914-9. doi: 10.1002/anie.201403765. Epub 2014 Jun 6.
A general synthesis of triazolium-containing [2]rotaxanes, which could not be accessed by other methods, is reported. It is based on a sequential strategy starting from a well-designed macrocycle transporter which contains a template for dibenzo-24-crown-8 and a N-hydroxysuccinimide (NHS) moiety. The sequence is: 1) synthesis by slippage of a [2]rotaxane building-block; 2) its elongation at its NHS end; 3) the delivery of the macrocycle to the elongated part of the axle by an induced translational motion; 4) the contraction process to yield the targeted [2]rotaxane and recycle the initial transporter.
报告了一种通用的三唑鎓[2]轮烷的合成方法,该方法无法通过其他方法获得。它基于一种从精心设计的大环转运体开始的顺序策略,该转运体包含二苯并-24-冠-8 的模板和 N-羟基琥珀酰亚胺(NHS)部分。该序列为:1)通过[2]轮烷建筑块的滑错合成;2)其 NHS 端的延伸;3)通过诱导平移运动将大环输送到轴的延伸部分;4)收缩过程得到目标[2]轮烷并回收初始转运体。