Glycosaminoglycan mimetic biomaterials. 2. Alkene- and acrylate-derivatized glycopolymers via cyanoxyl-mediated free-radical polymerization

Citation
D. Grande et al., Glycosaminoglycan mimetic biomaterials. 2. Alkene- and acrylate-derivatized glycopolymers via cyanoxyl-mediated free-radical polymerization, MACROMOLEC, 34(6), 2001, pp. 1640-1646
Citations number
33
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
MACROMOLECULES
ISSN journal
00249297 → ACNP
Volume
34
Issue
6
Year of publication
2001
Pages
1640 - 1646
Database
ISI
SICI code
0024-9297(20010313)34:6<1640:GMB2AA>2.0.ZU;2-L
Abstract
Cyanoxyl ((OC)-O-. dropN)-mediated free-radical polymerization provides an effective and versatile method for engineering a diverse array of water-sol uble glycopolymers with high saccharide contents and low polydispersity ind exes (1.1 < M-w/M-n < 1.6). Cyanoxyl persistent radicals can be used as cha in-growth moderators of the statistical copolymerization of acrylamide with either nonsulfated or sulfated N-acetyl-D-glucosamine-carrying alkene- and acrylate-derivatized unprotected glycomonomers. Moreover, monosaccharide-c ontaining homopolymers can be prepared with some degree of control by polym erization of the acrylic glycomonomers.