Abstrakti
Crosslinked polystyrene beads were first functionalized with phenacyl ester linkers, and a series of four macrocycles with different ring sizes were synthesized from these linkers. The macrocycles were built from amide-linked monomers coupled by conventional peptide-synthesis methods. Annulation was achieved by copper(I)-catalyzed intramolecular azide–alkyne cycloaddition to give triazole linked macrocycles. The macrocycles were cleaved from the polymer beads with hydrazinolysis or saponification. The structures of macrocycles were confirmed by high-resolution nuclear magnetic resonance (NMR) and liquid chromatography–mass spectrometry (LC–MS) analysis. The ability of the polymers to selectively bind compounds from a mixture of aromatic derivatives in ethanol was tested. The prepared polystyrene supported macrocycles were found to selectively bind bromophenol blue and bromocresol green non-covalently with an association constant of 160–490 M−1.
Alkuperäiskieli | Englanti |
---|---|
Sivut | 24-30 |
Julkaisu | Reactive and Functional Polymers |
Vuosikerta | 89 |
DOI - pysyväislinkit | |
Tila | Julkaistu - huhtik. 2015 |
OKM-julkaisutyyppi | A1 Julkaistu artikkeli, soviteltu |