Kandrnálová Markéta, Kokan Zoran, Havel Václav, Nečas Marek, Šindelář Vladimír
Department of Chemistry and RECETOX, Faculty of Science, Masaryk University, Kamenice 5, 625 00, Brno, Czech Republic.
Angew Chem Int Ed Engl. 2019 Dec 9;58(50):18182-18185. doi: 10.1002/anie.201908953. Epub 2019 Oct 30.
Reversible covalent bonds play a significant role in achieving the high-yielding synthesis of mechanically interlocked molecules. Still, only a handful of such bonds have been successfully employed in synthetic procedures. Herein, we introduce a novel approach for the fast and simple preparation of interlocked molecules, combining the dynamic bond character of bis(acyloxy)iodate(I) anions with macrocyclic bambusuril anion receptors. The proof of principle was demonstrated on rotaxane synthesis, with near-quantitative yields observed in both the classical and "in situ" approach. The rotaxane formation was confirmed in the solid-state and solution by the X-ray and NMR studies. Our novel approach could be utilized in the fields of dynamic combinatorial chemistry, supramolecular polymers, or molecular machines, as well inspire further research on molecules that exhibit dynamic behavior, but owing to their high reactivity, have not been considered as constituents of more elaborate supramolecular structures.
可逆共价键在实现机械互锁分子的高产率合成中起着重要作用。然而,在合成过程中成功应用的此类键却寥寥无几。在此,我们介绍一种快速简便制备互锁分子的新方法,该方法将双(酰氧基)碘酸根(I)阴离子的动态键特性与大环竹节环脲阴离子受体相结合。在轮烷合成中证明了该原理,在经典方法和“原位”方法中均观察到接近定量的产率。通过X射线和核磁共振研究在固态和溶液中证实了轮烷的形成。我们的新方法可用于动态组合化学、超分子聚合物或分子机器领域,也有望激发对表现出动态行为但因其高反应性而未被视为更复杂超分子结构组成部分的分子的进一步研究。