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Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition

Authors :
Kumawat, Lokesh K.
Wynne, Conor
Cappello, Emanuele
Fisher, Peter
Brennan, Luke E.
Strofaldi, Alessandro
McManus, Jennifer J.
Hawes, Chris S.
Jolliffe, Katrina A.
Gunnlaugsson, Thorfinnur
Elmes, Robert B. P.
Kumawat, Lokesh K.
Wynne, Conor
Cappello, Emanuele
Fisher, Peter
Brennan, Luke E.
Strofaldi, Alessandro
McManus, Jennifer J.
Hawes, Chris S.
Jolliffe, Katrina A.
Gunnlaugsson, Thorfinnur
Elmes, Robert B. P.
Publication Year :
2021

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 1 HNMR 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 HPO4 2 anion when compared against other biologically relevant anions

Details

Database :
OAIster
Notes :
text, Kumawat, Lokesh K. and Wynne, Conor and Cappello, Emanuele and Fisher, Peter and Brennan, Luke E. and Strofaldi, Alessandro and McManus, Jennifer J. and Hawes, Chris S. and Jolliffe, Katrina A. and Gunnlaugsson, Thorfinnur and Elmes, Robert B. P. (2021) Squaramide‐Based Self‐Associating Amphiphiles for Anion Recognition. ChemPlusChem, 86 (8). pp. 1058-1068. ISSN 2192-6506, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1401580214
Document Type :
Electronic Resource