Three types of novel N-[4-(NΠ-substituted aminocarbonyl)phenyl] maleimide (RPhMI: N-substituent (R) Ο phenyl, cyclohexyl, and cyclododecyl) were synthesized and homopolymerized under several conditions. In the copolymerizations of RPhMI (M 1 ) with styrene (ST; M 2 ) or methyl methacrylate (MMA; M 2
Photopolymerization of N-substituted phenyl maleimide initiated with N,N-dimethyl-4-toluidine
β Scribed by Guo Zhang Xu; Jian Hua Dong; Kun Yuan Qiu
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 184 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
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## Abstract The copolymerization of styrene with __N__βphenyl maleimide in the presence of organomodified montmorillonite or Na^+^ montmorillonite was investigated. The conversion of the monomer was determined dilatometrically or gravimetrically. The copolymerization rate was accelerated and the po
Asymmetric anionic homopolymerizations of achiral N-substituted maleimides (RMI) were performed with lithium 4-alkyl-2,2-dialkyloxazolidinylamide. All obtained polymers were optically active, exhibiting opposite optical rotation to that of a corresponding oxazolidinyl group at the terminal of the ma