Rate-enhancement of hydrolysis of long-chain amino acid ester by cross-linked polymers imprinted with a transition-state analogue: evaluation of ... [An article from: Analytica Chimica Acta]
Book Details
PublisherElsevier
ISBN / ASINB000RR00D8
ISBN-13978B000RR00D2
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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
Acceleration property of a cross-linked polymer catalyst for the hydrolysis of N-dodecanoyl leucine-p-nitrophenyl ester is attributed to the molecularly imprinting of phenyl-1-undecylcarbonylamino-3-methylbutyl phosphonate as the template of transition-state analogue (TSA) and 4-[(3'-methacryloylamino)ethyl]imidazole as the binding site of the polymer catalyst. Equimolar complex of the template of the TSA and the binding site of imidazole-containing monomer through the electrostatic interaction and hydrophobic effect was confirmed by ^1H NMR measurements and the complex was copolymerized with hydrophobic styrene monomer and 10% divinylbenzene cross-linker. A control polymer without the template, but with the cross-linker, was also prepared. After removal of the template, imidazole-containing imprinted polymer gave a ca. two-fold rate-enhancement in comparison to the non-imprinted polymer.
Description:
Acceleration property of a cross-linked polymer catalyst for the hydrolysis of N-dodecanoyl leucine-p-nitrophenyl ester is attributed to the molecularly imprinting of phenyl-1-undecylcarbonylamino-3-methylbutyl phosphonate as the template of transition-state analogue (TSA) and 4-[(3'-methacryloylamino)ethyl]imidazole as the binding site of the polymer catalyst. Equimolar complex of the template of the TSA and the binding site of imidazole-containing monomer through the electrostatic interaction and hydrophobic effect was confirmed by ^1H NMR measurements and the complex was copolymerized with hydrophobic styrene monomer and 10% divinylbenzene cross-linker. A control polymer without the template, but with the cross-linker, was also prepared. After removal of the template, imidazole-containing imprinted polymer gave a ca. two-fold rate-enhancement in comparison to the non-imprinted polymer.
