化学
对映体
磺酸盐
对映选择合成
羧酸盐
配体(生物化学)
水溶液
分子识别
组合化学
环番
离子
立体化学
超分子化学
手性(物理)
手性配体
结晶学
选择性
水介质
摩尔比
自组装
摩尔质量
有机阴离子
作者
Xiao‐Ni Han,Yu‐Jie Long,Ying Han,Zhi‐Qiang Hu,Chuan‐Feng Chen
摘要
ABSTRACT Selective π‐metalation of macrocyclic arenes (MAs) featuring large and stable chiral cavities remains a considerable challenge. Consequently, the recognition of the π‐metalated MAs toward bulky anions, especially organic and chiral anions, is attractive but remains unexplored. In this work, a new macrocyclic arene named nut[6]arene ( NA ) was reported, which showed a rigid hexagonal structure and stable chiral cavity. Starting from NA , a series of π‐metalated MAs were selectively synthesized. In particular, exo ‐tri‐metalated NA ( NA‐3Ru‐I ) with a C 3 symmetrical structure was selectively obtained in high yields by the modulation of ligand sterics, molar ratio, and reaction temperature, which showed a large and electron‐deficient cavity. Consequently, water‐soluble NA‐3Ru‐II could effectively bind large inorganic anions, including ReO 4 − and PF 6 − to form 1:1 stable host‐guest complexes. Especially, NA‐3Ru‐II showed strong binding abilities toward various organic sulfonate anions and carboxylate anions. Moreover, a pair of enantiomeric NA‐3Ru‐II was also obtained, and they exhibited enantioselective recognitions for chiral anionic guests in aqueous solution, providing a new chiral platform for anion recognition.
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