催化作用
磷酸
共价键
化学
多相催化
金属有机骨架
组合化学
有机化学
纳米技术
材料科学
吸附
作者
Wenqi Qiu,Jialin Cui,Kejin Zhu,Meng Gao,Xuhan Zheng,Hui Liu,Zongxia Guo,Zhenxiu Zhang,Yingjie Zhao
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-09-21
卷期号:14 (19): 14780-14786
被引量:23
标识
DOI:10.1021/acscatal.4c04877
摘要
Drawing inspiration from enzymatic catalysis, a phosphoric acid-based covalent organic framework ( PA-COF ) was engineered for the efficient synthesis of optically pure lactide. PA-COF catalyst features precisely engineered microenvironments within well-defined porous channels decorated with phosphoric acid as the catalytically active sites. Much like enzymatic catalysis, where product selectivity is governed by the protein pocket, PA-COF provides precise microenvironments due to its highly ordered channels and adjustable structures. The phosphoric acids in the channels as catalytically active sites play key roles in directly converting lactic acid monomers into the cyclic dimer lactide. The process effectively avoided oligomerization, achieving an excellent yield of approximately 95%. This approach significantly differs from the traditional two-step strategy. It avoids the use of metal catalysts and high-temperature (∼200 °C) reaction conditions, thus avoiding metal residues and racemization. This microenvironment effect catalysis strategy provides a new pathway for the synthesis of lactide and may be extended to other useful condensation reactions.
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