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Highly efficient, reversible iodine capture and exceptional uptake of amines in viologen-based porous organic polymers

A viologen-based porous organic polymer, POP-V-VI, was designed and synthesized by a facile nucleophilic substitution between cyanuric chloride and 1,2-bis(4-pyridinium) ethylene. Together with the reported POP-V-BPY with a similar structure, these viologen-based porous organic polymers bear high ch...

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Detalles Bibliográficos
Autores principales: Li, Meiting, Zhao, Huanyu, Lu, Zhong-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9054242/
https://www.ncbi.nlm.nih.gov/pubmed/35517750
http://dx.doi.org/10.1039/d0ra03242e
Descripción
Sumario:A viologen-based porous organic polymer, POP-V-VI, was designed and synthesized by a facile nucleophilic substitution between cyanuric chloride and 1,2-bis(4-pyridinium) ethylene. Together with the reported POP-V-BPY with a similar structure, these viologen-based porous organic polymers bear high charge density, phenyl ring and nitrogenous affinity sites, which endow them with excellent iodine vapor uptake capacity (4860 mg g(−1) for POP-V-VI and 4200 mg g(−1) for POP-V-BPY) and remarkably high adsorption capacity for pyridine (4470 mg g(−1) for POP-V-VI and 8880 mg g(−1) for POP-V-BPY) and other aliphatic amines. POP-V-VI and POP-V-BPY could be efficiently recycled and reused three times without significant loss of iodine vapor uptake. All these results demonstrate that POP-V-VI and POP-V-BPY are promising adsorbents for practical applications in portable devices such as gas masks.