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

ABSTRACT: 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.

SUBMITTER: Li M

PROVIDER: S-EPMC9054242 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

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

Li Meiting M Zhao Huanyu H Lu Zhong-Yuan ZY

RSC advances 20200528 35

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<sup>-1</sup> for POP-V-VI and 4200 mg g<sup>-1</sup> for POP-V-BPY) an ...[more]

PMID: 35517750

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