In this article, we review our studies concerning the design of novel functional polymers based on amino acids. Although an amino acid is the simplest optically active compound in the nature, its polymers, peptides, and proteins show a wide variety of functions such as electron transfer, information
Diketopiperazine-based polymers from common amino acids
β Scribed by J. Akerlund; S. Harmeier; J. Pumphrey; D. C. Timm; J. I. Brand
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 138 KB
- Volume
- 78
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
High-melting-point polymers with heterocyclic backbone units were synthesized from common amino acids. Acids were first converted to methyl ester salts and then were dimerized to form diketopiperazines, which were polymerized in solution. Aspartic acid, serine, lysine, glycine, and tyrosine were used as starting materials for the diketopiperazines. Aromatic and aliphatic comonomers were used. Thus, we demonstrate the technical feasibility of producing strong, durable resins from abundant domestic resources. These resins show great potential for high-performance polymers for use in films, fibers, and composites.
π SIMILAR VOLUMES
The purpose of this research was to synthesize new regular poly(ester amide)s (PEAs) consisting of nontoxic building blocks like hydrophobic β£-amino acids, β£,-diols, and aliphatic dicarboxylic acids, and to examine the effects of the structure of these building block components on some physico-chemi
Previous studies have demonstrated that the interaction of carboxylic acids with aryl amines produces free radicals that can initiate the polymerization of acrylic monomers. N-Aryl-a-amino acids (NAAA) represent a special class of this type of initiator that combines in one molecule the carboxylic a