The syntheses of random and block copolymers (using sequential monomer addition) of methyl methacrylate (MMA) and lauryl methacrylate (LMA) have been investigated by group transfer polymerization (GTP) over a wide composition range using tetrabutylammonium bibenzoate (TBABB) as catalyst and 1-methox
Polymerization of methyl methacrylate with achiral 4B group metallocene compounds
β Scribed by Hai Deng; Takeshi Shiono; Kazuo Soga
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 445 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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β¦ Synopsis
Abstract
Methyl methacrylate (MMA) was polymerized with Cp~2~ZrCl~2~/ methylalyminoxane or Cp~2~M(CH~3)~~2~ (M: Zr, Hf; Cp = cyclopentadienyl) combined with B(C~6~F~5~)~3~ (1) or Ph~3~CB(C~6~F~5~)~4~ (2), (Ph = phenyl). in the presence of a Lewis acid like Zn(C~2~H~5~)~2~ with slow inititation, which gave syndiotacticβrich poly(methyl methacrylate) (PMMA) with high molecular weight. The polymer yield increases with polymerization time, which indicates that the propagation rate is zero order in concentration of monomer. The polymer yield increases also with concentration of Cp~2~Zr(CH~3~)~2~.2, which indicates the zirconocene to be the real catalyst. The polymer yield and the initiation efficiency (N/[Zr]) increase with the concentration of Zn(C~2~H~5~)~2,~ which indicates Zn(C~2~H~5~)~2~, to be involved in the initiation. It is also shown that the propagation reaction is independent of the concentration of Zn(C~2~H~5~)~2~.
π SIMILAR VOLUMES
Hydroxyl functional azo compounds have been used as reducing agents in redox polymerization of methyl methacrylate (MMA) in conjunction with ceric ammonium nitrate (which acts as a n oxidizing agent in aqueous nitric acid a t 20Β°C). Kinetic measurements were followed by gravimetric method, at lower
## Abstract A divalent samarium complex that bears two bulky phenoxide ligands promotes the living polymerization of methyl methacrylate in the absence of cocatalyst. The initiation involves a tailβtoβtail coupling reaction of the samariumβenolate radical followed by a oneβelectron reduction of the