Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/62639
Title: Chiral recognition of amino acid esters by zinc porphyrin derivatives
Authors: Wang, CZ
Zhu, ZA
Li, Y
Chen, YT
Wen, X
Miao, FM
Chan, WL
Chan, ASC
Issue Date: 2001
Publisher: Royal Society of Chemistry
Source: New journal of chemistry, 2001, v. 25, no. 6, p. 801-806 How to cite?
Journal: New journal of chemistry 
Abstract: Three novel chiral zinc porphyrins (4a–4c) with protected chiral amino acid substituents as chiral sources were synthesized. Their chiral recognition of amino acid methyl esters was investigated using UV-vis spectrophotometric titration. Some enantioselectivities obtained are higher than that of the known system, and the highest achieved in our study is 21.54 using host 4a with PheOCH3 as guest. We also show that higher enantioselectivity can be obtained at lower temperature. Circular dichroism spectra of chiral porphyrin derivatives binding to enantiomers of guests show great shape and intensity differences. Molecular modeling was performed to understand chiral recognition on a molecular level, and the results are in good agreement with the experimental data.
URI: http://hdl.handle.net/10397/62639
ISSN: 1144-0546
DOI: 10.1039/B100942G
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