A General Group-Protection Synthesis Strategy to Fabricate Covalent Organic Framework Gels.


Journal

Journal of the American Chemical Society
ISSN: 1520-5126
Titre abrégé: J Am Chem Soc
Pays: United States
ID NLM: 7503056

Informations de publication

Date de publication:
06 Dec 2023
Historique:
medline: 27 11 2023
pubmed: 27 11 2023
entrez: 27 11 2023
Statut: ppublish

Résumé

Fabricating insoluble and infusible porous materials into gels for advanced applications is of great importance but has formidable challenges. Here, we present a general, facile, and scalable protocol to fabricate covalent organic framework (COF) gels using a group-protection synthesis strategy. To prove the generality of this strategy, we successfully prepared 10 types of COF organohydrogels with high crystallinity, porosity, good mechanical properties, and excellent solvent and freezing resistance. Notably, these COF organohydrogels can easily transform into hydrogels, organogels, and aerogels, breaking the gaps between different types of COF gels. An in-depth mechanism investigation unveils that the group-protection strategy effectively slows down the formation rate and regulates the morphology of COFs, benefiting the formation of cross-linked nanofibers/nanosheets to produce COF gels. We also find that the hydrogen bond network formed by the organic/water binary solvent and functional groups in the COF skeletons plays a vital role in creating organohydrogels and maintaining frost resistance and solvent resistance. As an application demonstration, COF gels installed with photoresponsive azobenzene groups show excellent solar energy absorption, photothermal conversion, and water transmission performances, demonstrating great potential in solar desalination. This work enriches the synthesis toolboxes for COF gels and expands the application scope of COFs.

Identifiants

pubmed: 38011228
doi: 10.1021/jacs.3c09284
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

26266-26278

Auteurs

Shuping Jia (S)

College of Chemistry, Nankai University, Tianjin 300071, China.
Xinjiang Key Laboratory of Novel Functional Materials Chemistry, College of Chemistry and Environmental Sciences, Kashi University, Kashi 844000, China.

Yujie Liu (Y)

College of Chemistry, Nankai University, Tianjin 300071, China.

Liqin Hao (L)

College of Chemistry, Nankai University, Tianjin 300071, China.

Jiayu Ni (J)

State Key Laboratory of Separation Membranes and Membrane Processes, School of Materials Science and Engineering, Tiangong University, Tianjin 300387, China.

Yanjie Wang (Y)

State Key Laboratory of Separation Membranes and Membrane Processes, School of Materials Science and Engineering, Tiangong University, Tianjin 300387, China.

Yi Yang (Y)

College of Chemistry, Nankai University, Tianjin 300071, China.

Yao Chen (Y)

State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, China.

Peng Cheng (P)

College of Chemistry, Nankai University, Tianjin 300071, China.
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin 300071, China.

Li Chen (L)

State Key Laboratory of Separation Membranes and Membrane Processes, School of Materials Science and Engineering, Tiangong University, Tianjin 300387, China.

Zhenjie Zhang (Z)

College of Chemistry, Nankai University, Tianjin 300071, China.
State Key Laboratory of Medicinal Chemical Biology, Nankai University, Tianjin 300071, China.
Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center, Frontiers Science Center for New Organic Matter, Nankai University, Tianjin 300071, China.

Classifications MeSH