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Facile construction of fully sp(2)-carbon conjugated two-dimensional covalent organic frameworks containing benzobisthiazole units

Developing a facile strategy for the construction of vinylene-linked fully π-conjugated covalent organic frameworks (COFs) remains a huge challenge. Here, a versatile condition of Knoevenagel polycondensation for constructing vinylene-linked 2D COFs was explored. Three new examples of vinylene-linke...

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Detalles Bibliográficos
Autores principales: Wang, Yuancheng, Hao, Wenbo, Liu, Hui, Chen, Renzeng, Pan, Qingyan, Li, Zhibo, Zhao, Yingjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8748616/
https://www.ncbi.nlm.nih.gov/pubmed/35013158
http://dx.doi.org/10.1038/s41467-021-27573-1
Descripción
Sumario:Developing a facile strategy for the construction of vinylene-linked fully π-conjugated covalent organic frameworks (COFs) remains a huge challenge. Here, a versatile condition of Knoevenagel polycondensation for constructing vinylene-linked 2D COFs was explored. Three new examples of vinylene-linked 2D COFs (BTH-1, 2, 3) containing benzobisthiazoles units as functional groups were successfully prepared under this versatile and mild condition. The electron-deficient benzobisthiazole units and cyano-vinylene linkages were both integrated into the π conjugated COFs skeleton and acted as acceptor moieties. Interestingly, we found the construction of a highly ordered and conjugated D-A system is favorable for photocatalytic activity. BTH-3 with benzotrithiophene as the donor with a strong D-A effect exhibited an attractive photocatalytic HER of 15.1 mmol h(−1)g(−1) under visible light irradiation.