Abstract
p-tert-Butylcalix[8]arene-octaacetic acid octaethyl ester and calix[8]arene-octaacetic acid octaethyl ester well recognized 2-phenylethylamine and phenylalanine methyl ester compared with the corresponding calix[6]arene derivatives. Moreover, the calix[8]arene derivatives, especially one having tert-butyl groups, gave better selectivity against biologically active amines having a complicated structure, such as norephedrine. We considered the interaction between calixarenes and organic ammonium ions from the viewpoint of molecular symmetries.
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Katsu, T., Okaki, N., Watanabe, K. et al. Comparative Study of the Response of Membrane Electrodes Based on Calix[6]arene and Calix[8]arene Derivatives to Organic Ammonium Ions. ANAL. SCI. 19, 771–774 (2003). https://doi.org/10.2116/analsci.19.771
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DOI: https://doi.org/10.2116/analsci.19.771