Click Reactivity of Azide-Modified Polyvinyl Chloride as an Entry to Glycopolymer Scaffolds

dc.contributor.authorAy, E
dc.contributor.authorYenil, N
dc.date.accessioned2025-04-10T10:25:47Z
dc.date.available2025-04-10T10:25:47Z
dc.description.abstractWe report the synthesis of new carbohydrate/triazole polymers based on poly(viny chloride) (PVC). Azide incorporation into commercially available PVC was carried out using nucleophilic substitution and Cu-catalyzed reaction of the resulting PVC-N-3 using three alkynyl-containing acetonide-protected monosaccharides (based on D-glucose and D-galactose) provided a set of PVC-based polymers incorporating a triazolyl linkage with monosaccharide moieties present on the periphery. Modified polymers were characterized by using Fourier transform infrared (FT-IR), Nuclear Magnetic Resonance (H-1-NMR and C-13-NMR) spectroscopy, together with thermogravimetric and surface morphological analysis.
dc.identifier.e-issn1334-417X
dc.identifier.issn0011-1643
dc.identifier.urihttp://hdl.handle.net/20.500.14701/33545
dc.language.isoEnglish
dc.titleClick Reactivity of Azide-Modified Polyvinyl Chloride as an Entry to Glycopolymer Scaffolds
dc.typeArticle

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