亚胺
化学
选择性
溴
膜
离子键合
组合化学
锂(药物)
聚合物
渗透
材料科学
频道(广播)
有机化学
合理设计
笼子
高分子化学
纳米技术
盐(化学)
跨膜蛋白
作者
Ying Xu,Zhentao Luo,QingYan Liu,Yingxue Jin,Wenju Chang,Zian Lin,Jie Shen,Huaqiang Zeng
摘要
Despite extensive advancements in the design of artificial transporters for K+, Cl- and water, the development of Li+-selective systems has remained comparatively neglected, largely due to its smaller ionic radius and higher hydration energy that pose significant design challenges. To date, only three classes of artificial Li+ transporters have been reported. In this work, we introduce a novel fourth class of artificial Li+ channels, constructed from unique self-assembling organic imine cages that form membrane-spanning porous architectures. By incorporating bromine substituents, the resulting channel exhibits not only the highest Li+ transport activity (EC50 of 0.017 mol‰, relative to lipids) but also unprecedented selectivity, with Li+/Na+ and Li+/K+ selectivity factors of 44 and 52 respectively, marking a new benchmark in transmembrane Li+ transport performance.
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