合作性
氢键
化学
合作约束
分子
共价键
达布科
结晶学
非共价相互作用
三元络合物
三元运算
立体化学
结合位点
辛烷值
有机化学
生物化学
酶
计算机科学
程序设计语言
作者
Yan‐Long Ma,Hua Ke,Arto Valkonen,Kari Rissanen,Wei Jiang
标识
DOI:10.1002/anie.201711077
摘要
Positive cooperativity achieved through activating weak non-covalent interactions is common in biological assemblies but is rarely observed in synthetic complexes. Two new molecular tubes have been synthesized and the syn isomer binds DABCO-based organic cations with high orientational selectivity. Surprisingly, the ternary complex with two hosts and one guest shows a high cooperativity factor (α=580), which is the highest reported for synthetic systems without involving ion-pairing interactions. The X-ray single-crystal structure revealed that the strong positive cooperativity likely originates from eight C-H⋅⋅⋅O hydrogen bonds between the two head-to-head-arranged syn tube molecules. These relatively weak hydrogen bonds were not observed in the free hosts and only emerged in the complex. Furthermore, this complex was used as a basic motif to construct a robust [2+2] cyclic assembly, thus demonstrating its potential in molecular self-assembly.
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