摘要
Covalent organic frameworks (COFs) have functional synthons, diverse structures and feature-rich functionality. Herein, the combination of a linear linker NH2-{MMo6}-NH2with 4-connected tetrahedral tetrakis(4-formylphenyl)silicon building units produced three isostructural complexesM-Anderson-COFs with a 3-fold interpenetrated diamondoid network. Among them Mn-Anderson-COF exhibited the highest catalytic activity in the photodegradation of RhB and MB in water. The addition of different scavengers demonstrated that1O2and H2O2were primary reactive species to degrade the dyes. Moreover, using M-Anderson-COF as a catalyst, organic sulfides were almost completely oxidized with 100% sulfoxide/sulfone selectivity.
源语言 | 英语 |
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页(从-至) | 8548-8553 |
页数 | 6 |
期刊 | Journal of Materials Chemistry A |
卷 | 8 |
期 | 17 |
DOI | |
出版状态 | 已出版 - 7 5月 2020 |