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Polyphosphonate covalent organic frameworks.

Ke XuRobert OestreichTakin Haj Hassani SohiMailis LounasvuoriJean G A RuthesYunus ZorluJulia MichalskiPhilipp SeiffertTill StrothmannPatrik TholenA Ozgur YazaydinMarkus SutaVolker PresserTristan PetitChristoph JaniakJens BeckmannJörn Schmedt Auf der GünneGündoğ Yücesan
Published in: Nature communications (2024)
Herein, we report polyphosphonate covalent organic frameworks (COFs) constructed via P-O-P linkages. The materials are synthesized via a single-step condensation reaction of the charge-assisted hydrogen-bonded organic framework, which is constructed from phenylphosphonic acid and 5,10,15,20-tetrakis[p-phenylphosphonic acid]porphyrin and is formed by simply heating its hydrogen-bonded precursor without using chemical reagents. Above 210 °C, it becomes an amorphous microporous polymeric structure due to the oligomerization of P-O-P bonds, which could be shown by constant-time solid-state double-quantum 31 P nuclear magnetic resonance experiments. The polyphosphonate COF exhibits good water and water vapor stability during the gas sorption measurements, and electrochemical stability in 0.5 M Na 2 SO 4 electrolyte in water. The reported family of COFs fills a significant gap in the literature by providing stable microporous COFs suitable for use in water and electrolytes. Additionally, we provide a sustainable synthesis route for the COF synthesis. The narrow pores of the COF effectively capture CO 2 .
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