Polymerization of vinyl monomers using a novel trifunctional iniferter
β Scribed by Shu-Hui Qin; Kun-Yuan Qiu
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 153 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
β¦ Synopsis
A novel trifunctional iniferter with photoinduced and thermal chemical dissociation functional groups in one molecule, diethyl 2,3-dicyano-2,3-di(p-N,N-diethyldithiocarbamylmethyl)phenylsuccinate (DDDCS), was successfully synthesized. The bulk polymerizations of styrene and methyl methacrylate initiated by DDDCS under UV-light irradiation and heating, respectively, were studied. The polymerizations proceeded via a living polymerization process in both cases; that is, the conversion and molecular weight of the resulting polymer increased linearly with increased reaction time. The resulting polymers, containing β£and -N,N-diethyldithiocarbamyl end groups, served as macroiniferters for further block copolymerization. Electron paramagnetic resonance studies showed that DDDCS initiated as a photoiniferter under UV-light irradiation by reversible COS-bond dissociation and as a thermal iniferter under heating by reversible hexasubstituted COC-bond dissociation.
π SIMILAR VOLUMES
New vinyl monomers having an isoxazole heterocyclic group were synthesized and were polymerized in dimethylformamide using azobisisobutyronitrile as a free radical initiator. The dependence of the rate of polymerization on monomer and initiator concentrations was determined, as well as the activatio
The polymerization rate of methyl methacrylate photoinitiated by p-nitroacetanilide in the presence of triethylamine was measured as a function of the amine concentration in different media. The polymerization is more efficient in nonpolar medium (benzene/monomer). ESR studies show the formation of