对映选择合成
磷酸
催化作用
共价键
化学
化学稳定性
同种类的
有机化学
材料科学
聚合物
组合化学
手性(物理)
多相催化
化学工程
结晶度
有机催化
组分(热力学)
不对称氢化
手性拆分
作者
Mengsi Li,Peiyi Duan,Lei Li,Bing Jiao,Huimin Ding,Weixu Li,Bo Gui,Junliang Sun,Hui Lv,Cheng Wang
标识
DOI:10.1002/anie.202522928
摘要
Abstract The design of three‐dimensional covalent organic frameworks (3D COFs) incorporating chiral phosphoric acids represents a promising strategy to enhance enantioselectivity in asymmetric catalysis while providing good framework stability, but their development remains a significant challenge. Herein, by using the multivariate approach, we report the construction of two highly crystalline chiral phosphoric acid‐functionalized 3D COFs with the 4‐fold interpenetrated qtz topology. Notably, the resulting frameworks exhibit exceptional chemical stability, remaining crystallinity even in 12 M HCl, saturated NaOH, and boiling water. Moreover, benefiting from the confined chiral porous architecture, these COFs deliver good activity, enantioselectivity, and recyclability in asymmetric N, N ‐acetalization reactions, significantly outperforming their homogeneous analogues. This work not only reports a highly stable chiral phosphoric acid‐functionalized 3D COF for asymmetric catalysis, but also provides a foundation for constructing robust, reusable heterogeneous chiral organocatalysts.
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