Vinyl Ether Polymerization Radical

The resulting polymers are produced under mild and controlled conditions and are useful in adhesives and coatings as well as in other uses such as for polymer electrolytes in batteries and for viscosity.

Vinyl ether polymerization radical.

A new photoinitiating system for living cationic polymerization of vinyl ethers is reported. Polymerization rate in figure 5 the conversion of acrylate 1407 cm 1 and vinyl ether groups 1618 cm 1 are plotted as a function of vinyl ether content. Provided is a method for the polymerization of vinyl ethers catalyzed by complexes of a lithium salt and a polyether. A general and efficient access toward terminally functionalized poly vinyl ether s.

Vinyl ethers 1 which have a strongly electron donating alkoxy substituent readily form polymers on treatment with an acidic compound initiator the polymerization is thus cationic in nature. A novel uv curing vinyl ether lcs with a wide temperature range was developed by mixturing various vinyl ether lc monomers. The pdvlc pdcvlc and f pdcvlc qds films were prepared by dual step polymerization of acrylate monomers radical polymerization and vinyl ether lc monomers cationic polymerization. The photoinitiated cationic polymerization of vinyl ether ve monomers has been studied by real time infrared spectroscopy.

It is remarkable that only 10 addition of dve 3 increases the conversion of the acrylate from. Radical cationic acrylate vinyl ether radical figure 5. This method however is highly sensitive to monomer structure and achieved only 76 m and 64 m in the case of n butyl bve and ethyl vinyl ether eve respectively. Macromolecules 2020 53 5 1536 1542.

Thienyl chloride initiated living cationic polymerization. In the current approach visible light irradiation of dimanganese decacarbonyl mn 2 co 10 in the presence of an alkyl bromide results in the formation of carbon centered radicals the photochemically generated radicals were then oxidized by diphenyliodonium ions to the corresponding cations. In order to overcome the challenge of direct radical polymerization of vinyl ethers commercial hydroxy functional vinyl ethers such as 2 hydroxyethyl vinyl ether heve were subjected to free radical polymerization generating. For the divinyl ether of triethylene glycol the chain reaction was shown to develop rapidly and extensively with kinetic chain lengths on the order of 10 000.

A preferred complex is a complex of lithium tetrafluoroborate and a glyme.