Synthesis and radical polymerization of a vinyl monomer having a sulfonylacylurea moiety and hydrolysis of the obtained polymer
โ Scribed by Takeru Iwamura; Ikuyoshi Tomita; Masato Suzuki; Takeshi Endo
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 139 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
The radical polymerization of N-acryloyl-N-(p-tolylsulfonyl)urea ( 2), prepared easily by the reaction of p-toluenesulfonyl isocyanate with acrylamide, was carried out in DMF, DMSO, or NMP at 60ะC by use of AIBN as an initiator to give a polymer 3 in a good yield. Copolymerization parameters of 2 were evaluated by the copolymerization with MMA. Polymer 3 was readily hydrolyzed in an aqueous NaOH solution (1 M) at room temperature to give poly(acrylic acid). The reason for the higher activity for hydrolysis of 3 compared to an ordinary amide is discussed.
๐ SIMILAR VOLUMES
A vinyloxy monomer having an electron-accepting chromophore moiety, p-((vinyloxy)methyl)benzonitrile (VOMBN), was synthesized by reaction of p-(hydroxymethyl)benzonitrile with ethyl vinyl ether (EVE) in the presence of mercuric acetate. VOMBN can easily be cationically homopolymerized and copolymeri
A vinyloxy monomer bearing electron-accepting chromophore, N-(2-(vinyloxy)ethyl)-1,8-naphthalimide (VOENI), was synthesized by reaction of potassium 1,8naphthalimide with 2-chloroethyl vinyl ether. VOENI can be homopolymerized by cationic initiation and copolymerized with maleic anhydride (MAn) unde