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

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-s...

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Detalles Bibliográficos
Autores principales: Chen, Tao, Li, Wen-Qian, Hu, Wei-Bo, Hu, Wen-Jing, Liu, Yahu A., Yang, Hui, Wen, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064649/
https://www.ncbi.nlm.nih.gov/pubmed/35520569
http://dx.doi.org/10.1039/c9ra02934f
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author Chen, Tao
Li, Wen-Qian
Hu, Wei-Bo
Hu, Wen-Jing
Liu, Yahu A.
Yang, Hui
Wen, Ke
author_facet Chen, Tao
Li, Wen-Qian
Hu, Wei-Bo
Hu, Wen-Jing
Liu, Yahu A.
Yang, Hui
Wen, Ke
author_sort Chen, Tao
collection PubMed
description 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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spelling pubmed-90646492022-05-04 Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions Chen, Tao Li, Wen-Qian Hu, Wei-Bo Hu, Wen-Jing Liu, Yahu A. Yang, Hui Wen, Ke RSC Adv Chemistry 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). The Royal Society of Chemistry 2019-06-07 /pmc/articles/PMC9064649/ /pubmed/35520569 http://dx.doi.org/10.1039/c9ra02934f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Chen, Tao
Li, Wen-Qian
Hu, Wei-Bo
Hu, Wen-Jing
Liu, Yahu A.
Yang, Hui
Wen, Ke
Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions
title Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions
title_full Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions
title_fullStr Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions
title_full_unstemmed Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions
title_short Direct synthesis of covalent triazine-based frameworks (CTFs) through aromatic nucleophilic substitution reactions
title_sort direct synthesis of covalent triazine-based frameworks (ctfs) through aromatic nucleophilic substitution reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9064649/
https://www.ncbi.nlm.nih.gov/pubmed/35520569
http://dx.doi.org/10.1039/c9ra02934f
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