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DOI 10.1002/marc.202300406

Медицинская библиотека · Macromolecular rapid communications · 2023

Water-Soluble Squaramide-Functionalized Copolymers for Anion Recognition.

Lane Jakob D E, Shiels Gabrielle, Ramamurthi Parathan, Müllner Markus, Jolliffe Katrina A

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Аннотация

A series of ethylene glycol-based squaramide-containing copolymers are synthesized via a post-polymerization functionalization strategy. Conversion of polymeric amines to squaramides is found to proceed in good yields, representing a versatile method of incorporating squaramides into polymers for anion recognition. Analysis of the polymers by UV-Vis and fluorescence spectroscopy revealed that anion binding takes place similarly to that of small-molecule squaramides. The presence of a fluorescent sensing group on polymer-bound squaramides allowed for a fluorescent sensing mechanism for anions that followed a similar trend in selectivity in aqueous DMSO solution, with selectivity observed for H2PO4 -, AcO- and SO4 2- over other common anions tested. The anion response and selectivity towards anions is similar to that of analogous small-molecule squaramides, however polymeric squaramides exhibited a greater resistance to deprotonation by more basic anions, which is attributed to the closer proximity of individual squaramides on a macromolecule. The squaramide-containing polymers exhibited good water solubility, overcoming a common problem for anion sensors which are typically not sufficiently soluble in water to function in many required applications. Despite no anion binding being observed in water, this study represents a simple and effective method of creating fully water-soluble anion receptors which may be adapted to give improved binding affinity and selectivity depending on the anion binding moiety.

Для цитирования: Lane Jakob D E, Shiels Gabrielle, Ramamurthi Parathan, Müllner Markus, Jolliffe Katrina A. Water-Soluble Squaramide-Functionalized Copolymers for Anion Recognition.. Macromolecular rapid communications. 2023. DOI: 10.1002/marc.202300406.

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