4.8 Article

Repositioning Chloride Transmembrane Transporters: Transport of Organic Ion Pairs

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 21, Pages 6921-6925

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201900818

Keywords

calix[6]arene; ion transport; membranes; receptors; supramolecular chemistry

Funding

  1. Fonds pour la Formation a la Recherche dans l'Industrie et dans l' Agriculture (FRIA-FRS, Belgium)
  2. European Research Council [802727]
  3. European Research Council (ERC) [802727] Funding Source: European Research Council (ERC)

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Given the biological importance of organic cations, the facilitated transport of organic ion pairs could find many applications. Calix[6]arene tris(thio)ureas, which possess a cavity that can accommodate primary ammonium ions, can not only act as carriers for Cl-/NO3- antiport but can also perform the cotransport of PrNH3Cl. Transport was monitored by fluorescence spectroscopy and the presence of the different species inside the vesicles was characterized by H-1 and Cl-35 NMR experiments involving shift reagents. The cotransport of PrNH3Cl was also observed by receptors deprived of a cavity, but the presence of the cavity conveys an advantage, as the cotransport by calix[6]arenes was observed to be more efficient than the Cl-/NO3- antiport, which is not the case with receptors without a cavity. The role played by the cavity was further highlighted by the disappearance of this advantage when using a bulky ammonium ion, which cannot be complexed within the cavity.

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