Abstract
In a one-pot synthesis, highly branched synthetic glycopolymers have been prepared using the 'Strathclyde Methodology' involving a protected galactose monomethacrylate, a branching comonomer (ethylene glycol dimethacrylate or divinylbenzene) and a chain transfer agent (dodecanethiol) with 2,2'-azo-bis-isobutyronitrile as the source of radicals. Branching was confirmed via MALS/SEC and (l)H NMR spectroscopy. One attractive feature of the methodology employed is that in a single-step procedure highly branched polymers with molar masses over a range of two orders of magnitude were obtained by fine-tuning the composition of comonomer and chain transfer agent mole feed ratio. Deprotection of the isopropylidene galactose functionalities on the polymers was achieved, leading to water-soluble and potentially bio-compatible synthetic glycopolymers with branched main chain architecture. (c) 2008 Elsevier Ltd. All rights reserved.
| Original language | English |
|---|---|
| Pages (from-to) | 1524-1533 |
| Number of pages | 10 |
| Journal | Reactive and Functional Polymers |
| Volume | 68 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Nov 2008 |
Keywords
- Conventional free-radical polymerisation
- Branched architecture
- Glycopolymer
- Water-soluble copolymers
- Facile synthesis
- GLYCOSAMINOGLYCAN-MIMETIC BIOMATERIALS
- TRANSFER RADICAL COPOLYMERIZATION
- POLY(METHYL METHACRYLATE)S
- HYPERBRANCHED GLYCOPOLYMERS
- RAFT POLYMERIZATION
- FACILE SYNTHESIS
- POLYMERS
- MONOMERS
- POLYDISPERSITY
- ARCHITECTURE