Département de Chimie, Centre de Recherche sur les Matériaux Avancés (CERMA), 1045 Ave. de la Médecine, Université Laval, Québec, G1V 0A6, Canada.
Molecules. 2010 May 25;15(5):3709-30. doi: 10.3390/molecules15053709.
The number of synthetic methods enabling the preparation of ammonium-based rotaxanes has increased very rapidly in the past ten years. The challenge in the synthesis of rotaxanes results from the rather weak interactions between the ammonium-containing rod and the crown ether macrocycle in the pseudorotaxane structure that rely mostly on O*H hydrogen bonds. Indeed, no strong base or polar solvent that could break up H-bonding can be used during the formation of rotaxanes because the two components will separate as two distinct entities. Moreover, most of the reactions have to be performed at room temperature to favor the formation of pseudorotaxane in solution. These non-trivial prerequisites have been taken into account to develop efficient reaction conditions for the preparation of rotaxanes and those are described in detail along this review.
在过去的十年中,能够制备铵基轮烷的合成方法的数量迅速增加。轮烷合成的挑战源于假轮烷结构中含铵的棒和冠醚大环之间的相互作用相当弱,主要依赖于 O*H 氢键。事实上,在轮烷的形成过程中不能使用能够破坏氢键的强碱或极性溶剂,因为这两个组分将作为两个不同的实体分离。此外,大多数反应必须在室温下进行,以有利于在溶液中形成假轮烷。这些非平凡的先决条件已经被考虑在内,以开发制备轮烷的有效反应条件,并在这篇综述中详细描述。