纳米反应器
共价键
催化作用
材料科学
纳米技术
不对称氢化
水溶液
组合化学
手性(物理)
相(物质)
双水相体系
金属有机骨架
化学工程
蚀刻(微加工)
催化加氢
聚合
自组装
化学
对映选择合成
手性固定相
定义明确
水介质
有机化学
高分子化学
纳米结构
作者
Jian‐Cheng Wang,Hua Qiao,Zhi Chen,Ting Sun,Ziran Liu,Cong‐Xue Liu,Xinran Zhang,Jin‐Qiu Li,Yu‐Bin Dong
出处
期刊:Small
[Wiley]
日期:2025-09-10
卷期号:21 (43): e07775-e07775
标识
DOI:10.1002/smll.202507775
摘要
The functionality of covalent organic frameworks (COFs) is usually highly related to their morphologies. Among various morphologies, the hollow-structured COFs have recently attracted intense attention due to their unique properties. Herein, the synthesis of hollow structured COFs are first reported with the chiral internal sites via combining the chiral templating method with the acid etching approach. After Rh(III)-metalation by postsynthetic modification, the generated hollow spherical CCOFs can be powerful chiral nanoreactors to highly promote the asymmetric hydrogenation of acetophenones in aqueous phase under mild conditions. The hollow structured heterosurface CCOFs may open a new way for their application in asymmetric catalysis.
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