4.2 Article

Phosphorylated amino derivatives of thiacalix [4] arene as membrane carriers: synthesis and host-guest molecular recognition of amino, hydroxy and dicarboxylic acids

Journal

JOURNAL OF PHYSICAL ORGANIC CHEMISTRY
Volume 27, Issue 1, Pages 57-65

Publisher

WILEY
DOI: 10.1002/poc.3236

Keywords

p-tert-butyl thiacalix[4]arenes; -aminophosphonates; organic acids; host-guest molecular recognition; membrane transport; HPLC

Funding

  1. Federal Program Research and scientific-pedagogical personnel of innovative Russia [16.740.11.0472]
  2. RFBR [12-03-90414-Ukr, 12-03-00252]

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Promising membrane transport and separation systems for selected dicarboxylic, -hydroxy- and -amino acids based on thiacalixarene platform have been developed. For the first time, p-tert-butyl thiacalix[4]arenes functionalized at the lower rim with aminophosphonate fragments have been obtained and characterized. As was established by UV-vis spectroscopy, membrane extraction and HPLC, the substitution of amino groups by -aminophosphonate units significantly enhances the selectivity of host molecules that bind to aspartic and glycolic acids. The aminophosphonate compounds synthesized can be used in the development of sensors and systems employed in the purification and separation of organic acids. Copyright (c) 2013 John Wiley & Sons, Ltd.

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