A series of aryl 1-propenyl ethers (ArPE) were prepared by the isomerization of the corresponding allyl aryl ethers (AArE) and used for photoinduced cationic polymerization studies. Attempted polymerization reactions using diaryliodonium salts as photoinitiators generally resulted in low yields of o
The preparation of novel 1-propenyl ethers and their cationic photopolymerization
✍ Scribed by J. V. Crivello; G. Löhden
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 896 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
A series of nine difunctional 1-propenyl ether monomers bearing ether, ester, carbonate, and urethane groups were prepared based on trimethylolpropane diallyl ether as the starting material. The monomers were fully characterized and then subjected to photoinitiated cationic polymerization using diaryliodonium salts as photoinitiators. The course of the polymerizations was followed using Fourier transform real-time infrared spectroscopy and the relative reactivities of the various monomers were determined. It could be shown that the differences in reactivity could be related mainly to the basicity of the functional group introduced into the molecule.
📜 SIMILAR VOLUMES
Several 1-butenyl and 1-pentenyl ether monomers were prepared by the ruthenium catalyzed multistage double bond isomerization of the corresponding 3-butenyl and 4-pentenyl ethers and characterized. Employing tris(triphenylphosphine)ruthenium(II) dichloride as a catalyst, the isomerization of octyl 4
1-Butenyl glycidyl ether was prepared in high yield by the rutheniumcatalyzed isomerization of crotyl glycidyl ether. This ambifunctional monomer underwent facile photoinitiated cationic polymerization using diaryliodonium salts as photoinitiators. The progress of the polymerizations was followed us