Radical polymerization of new functional monomers: Mono- and di-methacryloyl isocyanate containing bisphenol-s and its derivatives
โ Scribed by Der-Jang Liaw; Dung-Lang Ou
- Book ID
- 102660047
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 583 KB
- Volume
- 7
- Category
- Article
- ISSN
- 1042-7147
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โฆ Synopsis
New functional monomers mono-and di-methac yloyl isocyanate containing bisphenol-S were prepared on reaction of methacryloyl isocyanate (MAI) with bisphenol-S (BPS) and its derivatives at low temperature. The monomers thus obtained were characterized with elemental analysis, infrared, ultraviolet, ' H and 13C-NMR (nuclear magnetic resonance) spectra. Radical polymerization of mono-and di-methac yloyl isocyanate containing bisphenol-S and its derivatives was studied in terms of the rate of polymerizafion, solvent effect, thermal properties and kinetic measurements of photocrosslinking. Polar solvents such as dimethyl sulfoxide and dimethylacetamide (DMAc) were found to slow the polymeritation. Functional polymers containing the vinyl group of M A 1 were successfully modified and phatocrosslinked on irradiation in the presence of benzoin isopropyl ether. The photocrosslinking process follows second-order kinetics.
๐ SIMILAR VOLUMES
New functional monomers mono-and dimethacryloyl isocyanate containing bisphenol-A were prepared on reaction of methacryloyl isocyanate (MAI) with bisphenol-A (BPA) and its derivatives a t low temperature. The monomers thus obtained were characterized with IR, UV, and 'Hand I3C-NMR spectra. Radical p
The two new functional monomers, UMAI and UDMAI, having amide groups were prepared on reaction of methacryloyl isocyanate (MAI) with urea at low temperature. The monomers thus obtained were characterized by elemental analysis, as well as infrared, ultraviolet, 1 H and 13 C-NMR (nuclear magnetic reso
New functional monomer methacryloyl isocyanate containing 4-chloro-1phenol (CPHMAI) was prepared on reaction of methacryloyl isocyanate (MAI) with 4-chloro-1-phenol (CPH) at low temperature and was characterized with IR, 1 H, and 13 C-NMR spectra. Radical polymerization of CPHMAI was studied in term