Facile synthesis of a novel polymer/covalent organic framework@silica composite material in deep eutectic solvent for mixed-mode liquid chromatographic separation

The solvothermal synthesis of covalent organic framework (COF) modified silica gel usually requires the use of harmful organic solvents, tedious steps, and harsh reaction conditions. In pursuit of green chemistry, a new strategy for the facile preparation of COF@SiO 2 composite material was realized...

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Veröffentlicht in:Mikrochimica acta (1966) 2024-01, Vol.191 (1), p.35-35, Article 35
Hauptverfasser: Wei, Wanjiao, Zhao, Lulu, Liu, Yanjuan, Zhang, Yuefei, Chen, Wei, Tang, Sheng
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Sprache:eng
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Zusammenfassung:The solvothermal synthesis of covalent organic framework (COF) modified silica gel usually requires the use of harmful organic solvents, tedious steps, and harsh reaction conditions. In pursuit of green chemistry, a new strategy for the facile preparation of COF@SiO 2 composite material was realized in this work by using a low-toxicity and low-cost deep eutectic solvent as the reaction medium. Additionally, a flexible polyacrylic acid (PAA) was introduced for the purpose of improving the hydrophilic selectivity and separation efficiency of COF@SiO 2 . Based on the above ideas, a novel PAA/COF@SiO 2 composite was successfully developed as a liquid chromatographic packing material. Performance evaluation of the slurry-packed PAA/COF@SiO 2 column showed that diverse types of analytes were effectively separated, and the retention behavior of polar nucleosides showed a U-shaped trend, indicating mixed-mode of hydrophobic/hydrophilic retention mechanisms. Thermodynamic studies revealed that the separation mechanism was largely independent of temperature. This work verifies the feasibility of synthesizing polymer/COF@SiO 2 composite material in the deep eutectic solvent. This strategy provides a theoretical reference for the green and facile preparation of COF@SiO 2 as an efficient liquid chromatographic stationary phase. Graphical Abstract
ISSN:0026-3672
1436-5073
DOI:10.1007/s00604-023-06116-z