Synthesis and characterization of random and regular L-lysine-based polyamides
✍ Scribed by Isabelle Gachard; Bernard Coutin; Hikaru Sekiguchi
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 653 KB
- Volume
- 198
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
This paper deals with the synthesis of polyamides based on the natural diamine, L‐lysine, on the one hand, and diacids, adipic or glutaric, on the other hand. They were obtained by polycondensation of active diesters, pentachlorophenyl and pentafluorophenyl esters. L‐Lysine being non‐symmetrical, aregic (random) and syndioregic (“head‐to‐head, tail‐to‐tail”) poly(adipoyl‐L‐lysine)s and poly(glutaroyl‐L‐lysine)s were obtained with molecular weights higher than 15000; isoregic (“head‐to‐tail”) poly(adipoyl‐L‐lysine)s and poly(glutaroyl‐L‐lysine)s were prepared with lower molecular weights.
📜 SIMILAR VOLUMES
A novel series of cardo polyamides bearing the 2,2-adamantylidene unit were directly prepared from a new adamantane-based dietheramine, 2,2-bis[4-(4aminophenoxy)phenyl]adamantane, with various aromatic dicarboxylic acids using triphenyl phosphite (TPP) and pyridine as condensing agents. These polyam