4.6 Article

Facile construction of olefin-linked covalent organic frameworks for enhanced photocatalytic organic transformation via wall surface engineering

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 10, 期 13, 页码 7165-7172

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta09684b

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资金

  1. National Natural Science Foundation of China [22005001, 22001005, 22005002, 21805001, 51972001, 51772002]
  2. Academician workstation of Anhui University
  3. Anhui University Scientific Research Start-up Fund [S020118002/089, S020318006/005, S020118002/039, Y040418176]
  4. Changjiang Scholars and Innovative Research Team in University
  5. Key Lab of Photovoltaic and Energy Conservation Materials
  6. Chinese Academy of Sciences [PECL2019KF012]

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The exploration of fully conjugated covalent organic framework (COF)-based photocatalysts has become valuable research due to their excellent stability, outstanding semiconducting properties, and fascinating properties. In this study, three olefin-linked 2D COFs were designed and synthesized, demonstrating high crystallinity and preeminent stability. The COFs' pore wall surface was modified to induce distinct inductive and conjugative effects, which were then transmitted to the COF's backbone, allowing for regulation of the absorption range, band gap, and charge transfer efficiency. Among the COFs, the MeO-TBT-COF with a surface methoxy site exhibited the highest photocatalytic activity and recyclability. This study presents a facile strategy for the design and construction of olefin-linked COF-based photocatalysts through the tuning of the framework's pore wall surface groups.
Exploration of fully conjugated covalent organic framework (COF)-based photocatalysts has become valuable research owing to their excellent stability, outstanding semiconducting properties and fascinating properties. However, the design and construction of olefin-linked COF-based photocatalysts are still in an infant stage. Herein, three olefin-linked 2D COFs (F-TBT-COF, TBT-COF and MeO-TBT-COF) with high crystallinity and preeminent stability were designed and synthesized via the Knoevenagel condensation of aryl aldehyde monomers (F-TBT, H-TBT and MeO-TBT) and 2,4,6-trimethyl-1,3,5-triazine (TMT). Significantly, the pore wall surface of these COFs was docked with a single atom or unit to induce distinct inductive and conjugative effects. Then these effects transmitted to the COF's backbone, so that the absorption range, band gap and charge transfer efficiency of the COFs can be regulated via wall surface engineering. The MeO-TBT-COF with a surface methoxy site showed the highest photocatalytic activity and recyclability in the visible-light-driven C-3 thiocyanation reaction of indole derivatives and aerobic transformation of arylboronic acids to phenols. Therefore, we present a facile strategy to design and construct olefin-linked COF based photocatalysts via tuning the groups of the framework's pore wall surface.

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