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Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition

  • Lokesh K. Kumawat
  • , Conor Wynne
  • , Emanuele Cappello
  • , Peter Fisher
  • , Luke Brennan
  • , Alessandro Strofaldi
  • , Jennifer J. McManus
  • , Chris Samuel Hawes
  • , Katrina A. Jolliffe
  • , Thorfinnur Gunnlaugsson
  • , Robert B. P. Elmes

Research output: Contribution to journal › Article › peer-review

Abstract

The synthesis and characterisation of two novel self-assembled amphiphiles (SSAs) SQS-1 and SQS-2 are reported. Both compounds, based on the squaramide motif, were fully soluble in a range of solvents and were shown to undergo self-assembly through a range of physical techniques. Self-assembly was shown to favour the formation of crystalline domains on the nanoscale but also fibrillar film formation, as suggested by SEM analysis. Moreover, both SQS-1 and SQS-2 were capable of anion recognition in DMSO solution as demonstrated using 1H NMR and UV/Vis absorption spectroscopy, but displayed lower binding affinities for various anions when compared against other squaramide based receptors. In more competitive solvent mixtures SQS-1 gave rise to a colourimetric response in the presence of HPO42− that was clearly visible to the naked eye. We anticipate that the observed response is due to the basic nature of the HPO42− anion when compared against other biologically relevant anions.
Original languageEnglish
Pages (from-to)1058-1068
Number of pages11
JournalChemPlusChem
Volume86
Issue number8
DOIs
Publication statusPublished - 12 Jul 2021
Externally publishedYes

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