Monomers and polymers of 4-(N,N-diallylamino)pyridine functions
โ Scribed by Ji-Tao Huang; Qiang Wang; Jing-Wu Sun
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 118 KB
- Volume
- 77
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
โฆ Synopsis
4-(N,N-Diallylamino)pyridine (DAAP), N,N-diallylaminobenzene (DAAB), N,N,
๐ SIMILAR VOLUMES
A maleimide bearing electron-donating chromophore, N-(4-N,N-dimethylaminophenyI)maleimide (DMAPMI) was synthesized from N,N-dimethylaminoaniline and maleic anhydride in the presence of acetic anhydride and sodium acetate. DMAPMI can be easily copolymerized with vinyl acetate (VAc). In addition, it c
Three types of novel N-[4-(Nะ-substituted aminocarbonyl)phenyl] maleimide (RPhMI: N-substituent (R) ฯญ 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
Two novel acrylic monomers bearing aromatic tertiary amino groups, i.e., N-acryloyl-Nphenylpiperazine (APP) and N-methacryloyl-N'-phenylpiperazine (MPP) are synthesized by the reaction of N-phenylpiperazine and the corresponding acryloyl chlorides in the presence of triethylamine. They can be polyme
The title diamines were synthesized by condensation of 1,Cphenylenediamine with paraformaldehyde and a suitable phosphorus acid triester. The N,N'dibenzoyl derivatives of the above compounds were also prepared. New flame-retardant polyamides were synthesized under various experimental conditions by
New aromatic benzobisthiazole copolymers containing 10-70 mol % of 4-N,N-dimethylamino-triphenylamine functionality were prepared from the respective dinitrile or dicarboxylic acid monomers, terephthalic acid, and 2,5-diamino-1,4-benzenedithiol dihydrochloride in polyphosphoric acid. At the first ap