摘要
The efficient capture of myricetin is often challenged by its instability in alkaline environments, which contradicts the alkaline conditions required for traditional boronate affinity materials. To address this, a dual-recognition molecularly imprinted polymer (DMIP) supported on HOF-101 was developed using a deep eutectic solvent (DES)-driven strategy. A dual DES system was employed to achieve synergistic recognition: ternary DES 1 acts as a functional monomer combining boronate affinity and hydrogen bonding, while binary DES 2 serves as a green solvent and porogen. Crucially, the ethylene glycol in DES 2 facilitates “teamed boronate affinity” via B–O coordination, significantly lowering the p K a of boronic acid groups. This mechanism enables efficient specific recognition at pH 6.0, effectively overcoming the limitation of decreased affinity under weakly acidic conditions. The optimized BA-DES/DMIPs exhibited rapid equilibrium (20 min), a high Langmuir maximum adsorption capacity (45.016 mg/g), and excellent stability over five cycles. Furthermore, the material demonstrated superior selectivity against structural analogs and achieved satisfactory recovery rates (99.80%–101.67%) in grape juice, confirming its potential for green and efficient separation in complex matrices.
危险品化学品经营许可证(带存储)