𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Random and block 2-alkyl-2-oxazolines telechelic macromonomers

✍ Scribed by Philippe Guinot; Lonnie Bryant; Tak Yuen Chow; Takeo Saegusa


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
626 KB
Volume
197
Category
Article
ISSN
1022-1352

No coin nor oath required. For personal study only.

✦ Synopsis


Ring-opening polymerization of 2-methyl-2-oxazoline initiated by 2-@-nitrobenzenesulfonato)ethyl methacrylate follows the so-called "living mechanism", i. e. fast initiation compared to slow propagation and no chain transfer. Accordingly, methacryl macromonomers having homopolymers, block or random copolymers of 2-methyl and 2-pentyl-2-oxazoline backbones with narrow molecular weight distribution were obtained. Termination of the propagating species by ion-exchange or aminolysis with triethylamine yielded hydroxyl and quaternary ammonium terminated macromonomers, respectively.


📜 SIMILAR VOLUMES


Bis-macromonomers of 2-alkyl-2-oxazoline
✍ Darinka Christova; Rumiana Velichkova; Eric J. Goethals 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 299 KB

## Abstract Poly(2‐alkyl‐2‐oxazoline)s having an acrylate group at both chain ends were synthesized by terminating living bifunctional poly(2‐methyl‐2‐oxazoline) or poly(2‐ethyl‐2‐oxazoline) with acrylic acid. These macromonomers have been polymerized to the corresponding polyoxazoline networks. Th

Block and graft copolymers of 2-oxazolin
✍ Kobayashi, Shiro ;Saegusa, Takeo 📂 Article 📅 1985 🏛 Wiley (John Wiley & Sons) ⚖ 590 KB

This paper describes our recent developments of block and graft copolymers prepared by the cationic ringopening polymerization of 2-oxazolines. First, the mechanistic aspects of polymerization are mentioned, in which terms of "electrophilic and nucleophilic polymerizations" are proposed. Then, prepa

Synthesis and copolymerization of macrom
✍ Aurelia Groß; Gerhard Maier; Oskar Nuyken 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 753 KB

## Abstract Several macromonomers were prepared by cationic ring‐opening polymerization of 2‐nonyl‐ and 2‐phenyl‐2‐oxazoline using different techniques of functionalization. Introduction of the unsaturated functional group directly via a suitable termination agent proved to be superior to the use o