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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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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). |
format | Online Article Text |
id | pubmed-9064649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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