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January 16, 2026Chemistry - An Asian Journal1 citations

Pyridine and N ‐Pyridinium Functionalized Macrocyclic Squaramide Anion Receptors with High Affinity for Aqueous Sulfate

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TSThomas M. SalmonELEna T. LuisSBStephen M. Butler

Key Points

  • The study aims to improve the binding affinity of macrocyclic squaramide receptors for sulfate in aqueous environments.
  • Synthesis of macrocycles with pyridinium groups for charge-assisted interactions.
  • Evaluation of binding affinity for sulfate and selenate in pure water.
  • Assessment of binding stoichiometry under different conditions.
  • Pyridinium-enhanced receptors showed increased binding affinity for sulfate.
  • The ability to discriminate between sulfate and selenate was reduced.
  • Unexpected changes in binding stoichiometry were observed.

Abstract

ABSTRACT Macrocyclic squaramide‐containing receptors have previously been shown to bind sulfate with high selectivity and affinity in aqueous‐organic mixtures. To increase binding affinity of this class of hydrogen‐bonding receptors in pure water, macrocycles in which pyridinium groups have been inserted to provide additional charge‐assisted hydrogen‐bonding interactions were synthesized and their anion binding evaluated. The inclusion of charge‐assisted interactions provides enhanced binding affinity for sulfate in water but concomitantly reduces ability of the receptors to discriminate sulfate from the closely related selenate and leads to unexpected changes in binding stoichiometry.

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Cite This Study

Salmon et al. (2026) studied this question.

synapsesocial.com/papers/6969d4fd940543b977709de2https://doi.org/10.1002/asia.70547
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