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Mendeleev Communications, 2012, Volume 22, Issue 2, Pages 80–82
DOI: https://doi.org/10.1016/j.mencom.2012.03.009
(Mi mendc2746)
 

This article is cited in 13 scientific papers (total in 13 papers)

Selective transmembrane carriers for hydroxycarboxylic acids: Influence of a macrocyclic calix[4]arene platform

M. N. Agafonova, O. A. Mostovaya, I. S. Antipin, A. I. Konovalov, I. I. Stoikov

Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation
Abstract: Selective transmembrane carriers for a-hydroxy acids, acyclic a-amino phosphonates and calix[4]arenes containing a-aminophosphonate substituents at the lower rim have been synthesized; analytical HPLC has been used to monitor the selective separation of dicarboxylic, a-hydroxy and a-amino acid mixtures by membrane extraction; the attachment of a-aminophosphonate fragments to the macrocyclic calix[4]arene platform results in receptors with markedly modified efficiency and selectivity relative to those of only aminophosphonates.
Keywords: phosphonates, calix[4]arene, membrane extraction, carboxylic acids, amino acids, hydroxy acids, synthetic receptors.
Bibliographic databases:
Document Type: Article
Language: English


Citation: M. N. Agafonova, O. A. Mostovaya, I. S. Antipin, A. I. Konovalov, I. I. Stoikov, “Selective transmembrane carriers for hydroxycarboxylic acids: Influence of a macrocyclic calix[4]arene platform”, Mendeleev Commun., 22:2 (2012), 80–82
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  • This publication is cited in the following 13 articles:
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