Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions

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Abstract

Despite extensive efforts, only three main strategies have been developed to synthesize covalent triazine-based frameworks (CTFs) thus far. We report herein a totally new synthetic strategy which allows C-C bonds in the CTFs to be formed through aromatic nucleophilic substitution reactions. The as-synthesized CTF-1 and CTF-2 exhibited photocatalytic water splitting activity comparable to the CTFs made using ionothermal or Brønsted acid-catalyzed polymerization. Interestingly, CTF-2 distinguished itself by its two-photon fluorescence (emission at ∼530 nm under irradiation at either 400 nm or 800 nm).

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Chen, T., Li, W. Q., Hu, W. B., Hu, W. J., Liu, Y. A., Yang, H., & Wen, K. (2019). Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions. RSC Advances, 9(31), 18008–18012. https://doi.org/10.1039/c9ra02934f

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