MIPdatabase
Authors: Huangfu FY, Wang B, Sun Y
Article Title: Synthesis of molecularly imprinted polymers for chiral (S)-ibuprofen and their molecular recognition mechanism.
Publication date: 2013
Journal: Polymer-Korea
Volume: 37
Issue: (3)
Page numbers: 288-293.
DOI: 10.7317/pk.2013.37.3.288
Abstract: A group of molecularly imprinted polymers (MIPs) with specific recognition for chiral (S)-ibuprofen were successfully prepared based on hydrogen bonds, utilizing +¦-methacrylic acid as a functional monomer. The IR analysis of MIPs showed that the blue- and red-shifted hydrogen bonds were formed between templates and functional monomers in the process of self-assembly imprinting and re-recognition, respectively. According to UV-Vis analysis, we found that the ratio of host-guest complexes between template molecule and functional monomer was 1:1. The effect of cross-linker's quantity on the polymerization was studied by transmission electron microscope (TEM). The adsorption selectivity experiments indicated that MIPs exhibited higher selectivity to (S)-ibuprofen than those to ketoprofen and (R)-ibuprofen, (S)-ibuprofen's structural analogs
Template and target information: (S)-ibuprofen, ibuprofen
Author keywords: (S)-ibuprofen, chiral separation, hydrogen bond, molecularly imprinted polymer, Separation Factor
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