Al~tract---Methyl a-p-chlorobenzylacrylate and methyl :t-p-methoxybenzylacrylate were synthesized from dimethylmalonate by well known organic reactions. Both monomers were polymerizcd by a free-radical mechanism in benzene and their ceiling temperaturc determined. Comparison of the ceiling temperatu
Synthesis and free radical polymerization of p-methylseleno- and p-phenylselenostyrenes
โ Scribed by Tsugumichi Ando; Tae Seok Kwon; Akiko Kitagawa; Takahiro Tanemura; Shuji Kondo; Hideo Kunisada; Yasuo Yuki
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 383 KB
- Volume
- 197
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
โฆ Synopsis
Abstract
pโMethylselenostyrene (1) and pโphenylselenostyrene (2) as seleniumโcontaining vinyl monomers were prepared. Both monomers are readily polymerized free radically to afford the corresponding polymers having molecular weight of about 20 000 โผ 150 000. These homopolymers are stable below 300ยฐC. From the copolymerization with styrene, Q values of 1 and 2 were calculated to be 1,18 and 1,03, respectively. On the other hand, e values of these monomers are โ0,24 and โ0,04, respectively, indicating the electron withdrawing character of the seleno groups.
๐ SIMILAR VOLUMES
The free radical polymerization of p-tert-butoxystyrene (BOS) in the bulk at 125 "C "initiated" with the adduct of 2-benzoyloxy-l-phenylethyl and TEMPO (BS-TEMPO) was found to proceed in a "living" fashion, providing low-polydispersity PBOS and block copolymers of the type PBOS-b-PS, where TEMPO is
The radical polymerization of p-methacryloyloxybenzoic acid (MBA), at 60ยฐC in DMF followed classical kinetics, whereas that in p-dioxane did not as revealed by the rate being proportional to [MBA]'." [AIBN]'.". This could be explained by the dependency of the efficiency factorf on [MBA] and the pres