Department of Chemistry and Biochemistry, University of Montana, 32 Campus Dr, Missoula, MT, 59812, USA.
Angew Chem Int Ed Engl. 2016 Sep 26;55(40):12398-402. doi: 10.1002/anie.201605440. Epub 2016 Jul 14.
The self-assembly of higher-order anion helicates in solution remains an elusive goal. Herein, we present the first triple helicate to encapsulate iodide in organic and aqueous media as well as the solid state. The triple helicate self-assembles from three tricationic arylethynyl strands and resembles a tubular anion channel lined with nine halogen bond donors. Eight strong iodine⋅⋅⋅iodide halogen bonds and numerous buried π-surfaces endow the triplex with remarkable stability, even at elevated temperatures. We suggest that the natural rise of a single-strand helix renders its linear halogen-bond donors non-convergent. Thus, the stringent linearity of halogen bonding is a powerful tool for the synthesis of multi-strand anion helicates.
在溶液中,更高阶阴离子螺旋体的自组装仍然是一个难以实现的目标。在此,我们首次报道了一种三重螺旋体,它可以在有机和水相介质以及固态中包裹碘离子。这种三重螺旋体由三条三价芳烃炔基链自组装而成,类似于一个管状阴离子通道,内部排列着九个卤键供体。八个强碘······碘卤键和许多埋藏的π 面赋予了这个三聚体极高的稳定性,即使在高温下也是如此。我们认为,单链螺旋体的自然上升使其线性卤键供体不再汇聚。因此,卤键的严格线性是合成多链阴离子螺旋体的有力工具。