Affiliation:
1. College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education Shandong Normal University Jinan Shandong 250014 China
2. School of Light Industry and Engineering Qilu University of Technology (Shandong Academy of Sciences) Jinan Shandong 250353 China
Abstract
Comprehensive SummaryCovalent organic frameworks (COFs) driven photocatalytic organic transformations especially photooxidation reactions have become a fertile topic and attracted numerous research attentions. Boosting the charge generation and transport process is the key factor for achieving high catalytic efficiencies. As one of the most effective strategies, the introduction of “heavy atoms” into the long‐range ordered conjugated backbones can effectively facilitate the intersystem crossing (ISC) process and hence improve the generation of active oxygens, which is beneficial for the oxidation. In this work, we designed and synthesized a benzoselenadiazole based covalent organic framework (COF) material, BSe‐COF with heavy atom of selenium (Se), and a benzothiadiazole based BT‐COF with isomorphic backbone for comparison. Compared to BT‐COF, BSe‐COF exhibits broader absorption range, stronger photocurrent response and enhanced intersystem crossing (ISC) with higher singlet oxygen (1O2) generation efficiency. When applied in photocatalytic organic transformation, BSe‐COF presents remarkably higher photocatalytic activity in the oxidation of sulfides than BT‐COF under the irradiation of blue LED lamp. Furthermore, BSe‐COF can be used as efficient photocatalyst for the window ledge reaction with high yields (over 84%) of various sulfoxides from a wide range of thioether substrates scope.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Shandong Province
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献