Chiral α substituted acrylates side-chain polymers with a cinnamate core
✍ Scribed by J. M. Guglielminetti; G. Decobert; J. C. Dubois
- Book ID
- 105015924
- Publisher
- Springer
- Year
- 1986
- Tongue
- English
- Weight
- 930 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0170-0839
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract Poly‐N‐substituted glycines or “peptoids” are protease‐stable peptide mimics. Although the peptoid backbone is achiral and lacks hydrogen‐bond donors, substitution with α‐chiral side chains can drive the formation of stable helices that give rise to intense CD spectra. To systematically
Polymers of acrylic acid with uniform polystyrene side chains were synthesized by copolymerization of polystyrene macromer with acrylic acid. The products were purified by extractions with water and toluene and characterized with GPC, i.r., TEM and membrane osmometry. The average grafting number dec