Synthesis and radical polymerization behavior of N-vinylsaccharin (1) are described. Radical homopolymerization of 1 was carried out in the presence of a radical initiator for 24 h to afford the polymer containing a saccharin moiety in the side group, which was insoluble in common organic solvents.
Radical polymerization of benzyl N-(2,6-dimethylphenyl)itaconamate
β Scribed by Tsuneyuki Sato; Takashi Kitajima; Makiko Seno
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 216 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
The polymerization of benzyl N- (2,6-dimethylphenyl)itaconamate (BDMPI) with benzoyl peroxide (BPO) in N,N-dimethylformamide (DMF) was studied kinetically by ESR. The polymerization rate (R p ) at 70ΠC was given by R p Γ k[BPO] 0.78 [BDMPI] 1.1 . The overall activation energy of polymerization was determined to be 83.7 kJ/mol. The number-average molecular weight of poly(BDMPI) was in the range of 1500-2000 by gel permeation chromatography. From the ESR study, the polymerization system was found to involve ESR-observable propagating radicals of BDMPI under practical polymerization conditions. Using the polymer radical concentration by ESR, the rate constants of propagation (k p ) and termination (k t ) were determined in the temperature range of 50-70ΠC. The k p value seemed dependent on the chain-length of propagating radical. The analysis of polymers by the MALDI-TOF mass spectrometry suggested that most of the resulting polymers contain the dimethylamino terminal group. The copolymerization of BDMPI (M 1 ) and styrene (M 2 ) at 50ΠC in DMF gave the following copolymerization parameters; r 1 Γ 0.49, r 2 Γ 0.26, Q 1 Γ 1.2, and e 1 Γ /0.63. The thermal behavior of poly(BDMPI) was examined by dynamic thermogravimetry and differential scanning calorimetry.
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