Covalent molecular imprinting of bisphenol A using its diesters followed by the reductive cleavage with LiAlH(4).

J Chromatogr B Analyt Technol Biomed Life Sci

Graduate School of Science and Technology, Kobe University, 1-1 Rokkodai-cho, Nada-ku, Kobe 657-8501, Japan.

Published: May 2004

Bisphenol A (BPA) recognition materials were synthesized by a covalent imprinting technique using BPA-dimethacrylate or BPA-diacrylate as the template monomer. Binding sites in the polymers consisted of two hydroxyl groups that are generated by reducing the ester bonds of the template monomer with lithium aluminum hydride. The polymers strongly adsorbed BPA and structurally related compounds, however, other endocrine disruptors were hardly adsorbed. The BPA-dimethacrylate-based polymer interacted with the samples more strongly than the BPA-diacrylate-based polymer.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jchromb.2003.12.031DOI Listing

Publication Analysis

Top Keywords

template monomer
8
covalent molecular
4
molecular imprinting
4
imprinting bisphenol
4
bisphenol diesters
4
diesters reductive
4
reductive cleavage
4
cleavage lialh4
4
lialh4 bisphenol
4
bisphenol bpa
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!