催化作用
化学
小型商用车
选择性
协同催化
金属
葡萄糖酸
金属有机骨架
可重用性
四氢呋喃
组合化学
单层
有机化学
化学工程
光化学
吸附
程序设计语言
工程类
生物化学
软件
计算机科学
溶剂
作者
Wenjie Shi,Lingyun Cao,Hua Zhang,Xin Zhou,Bing An,Zekai Lin,Rui‐Han Dai,Jianfeng Li,Cheng Wang,Wenbin Lin
标识
DOI:10.1002/anie.201703675
摘要
Microenvironments in enzymes play crucial roles in controlling the activities and selectivities of reaction centers. Herein we report the tuning of the catalytic microenvironments of metal-organic layers (MOLs), a two-dimensional version of metal-organic frameworks (MOFs) with thickness down to a monolayer, to control product selectivities. By modifying the secondary building units (SBUs) of MOLs with monocarboxylic acids, such as gluconic acid, we changed the hydrophobicity/hydrophilicity around the active sites and fine-tuned the selectivity in photocatalytic oxidation of tetrahydrofuran (THF) to exclusively afford butyrolactone (BTL), likely a result of prolonging the residence time of reaction intermediates in the hydrophilic microenvironment of catalytic centers. Our work highlights new opportunities in using functional MOLs as highly tunable and selective two-dimensional catalytic materials.
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