Vinyl Ether Cationic Polymerization

Stereoselective cationic polymerization of vinyl ethers by easily and finely tunable titanium complexes prepared from tartrate derived diols.

Vinyl ether cationic polymerization.

However gaining photocontrol over chain growth would expand the utility of these methods and facilitate the design of novel complex architectures. In the presence of 2 6 dimethylpyridine as an added base living cationic polymerization of isobutyl vinyl ether was achieved in n hexane at 0 to 40 c with the 1 isobutoxy ethyl acetate. Herein the unique polymerization is reviewed along with the history of ring expansion polymerization. Macromolecules 26 1643 1649 1993.

Living cationic copolymerization of amide functional vinyl ethers with isobutyl vinyl ether ibve was achieved using sncl 4 in the presence of ethyl acetate at 0 c. A photoinitiating system for controlled cationic polymerization of isopropyl vinyl ether ipve was developed using diaryliodonium salts as the photoinitiator. Cationic polymerization of vinyl ethers controlled by visible light journal of the american chemical society photoinitiated cationic polymerizations are widely used in industrial processes. Poly vinyl ether s pves are useful materials of different applications.

This article is part of the themed collection. In situ direct nmr analysis of the growing species. In this work we have developed a versatile and highly efficient initiation approach based on thienyl chloride derivatives with readily available starting materials for the living cationic polymerization of vinyl ethers. Isospecific polymerization and recognition of chiral side chains titanium complexes of α α α α tetraaryl 1 3 dioxolane 4 5 dimethanol taddol derived from naturally abundant tartaric acid were demonstrated to function as highly effective.

Living cationic polymerization of isobutyl vinyl ether by hydrogen chloride lewis acid initiating systems in the presence of salts. Uv irradiation triggered the degradation of diphenyliodonium iodide which was followed by the controlled polymerization of ipve mediated by long lived propagating species. We have achieved ring expansion living cationic polymerization of vinyl ethers using designer cyclic initiator 1 that contained a hemiacetal ester. The number average molecular weight of the obtained polymers increased in direct proportion to the monomer conversion with relatively low polydispersity and the amide functional monomer units were introduced almost quantitatively.