Cargando…

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...

Descripción completa

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
Descripción
Sumario: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).