Aryl-triazole foldamers incorporating a pyridinium motif for halide anion binding in aqueous media

Aryl-triazole foldamers incorporating a pyridinium motif for halide anion binding in aqueous media

Aryl-triazole oligomers incorporating a pyridinium motif have been synthesized from their pyridine precursors. Anion binding studies show that methylation of the pyridine units can significantly enhance the halide anion affinities of the folded oligomers so that the foldamers are capable of binding...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2016-01, Vol.52 (24), p.4505-4508
Hauptverfasser: Shang, Jie, Zhao, Wei, Li, Xichen, Wang, Ying, Jiang, Hua
Format: Artikel
Sprache:eng
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Affinity
Anions
Binding
Halides
Methylation
Oligomers
Precursors
Pyridines
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container_issue 24
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container_title Chemical communications (Cambridge, England)
container_volume 52
creator Shang, Jie
Zhao, Wei
Li, Xichen
Wang, Ying
Jiang, Hua
description Aryl-triazole oligomers incorporating a pyridinium motif have been synthesized from their pyridine precursors. Anion binding studies show that methylation of the pyridine units can significantly enhance the halide anion affinities of the folded oligomers so that the foldamers are capable of binding halide anions in aqueous solutions.
doi_str_mv 10.1039/c5cc10422j
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source Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection
subjects Affinity
Anions
Binding
Halides
Methylation
Oligomers
Precursors
Pyridines
title Aryl-triazole foldamers incorporating a pyridinium motif for halide anion binding in aqueous media
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