## Abstract Copolymerization of styrene (St) and methyl methacrylate (MMA) was carried out using 1,1,2,2‐tetraphenyl‐1,2‐bis (trimethylsilyloxy) ethane (TPSE) as initiator; the copolymerization proceeded via a “living” radical mechanism and the polymer molecular weight (__M__~__w__~) increased with
Model copolymerization reactions. Initiation of the copolymerization of methyl methacrylate and acrylonitrile by 1,1′-azobis(1-phenyl[1-13C]ethane)
✍ Scribed by Douglas A. Cywar; David A. Tirrell
- Book ID
- 103075529
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 434 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
The copolymerization of methyl methacrylate (MMA) and acrylonitrile (A) was initiated by photolysis of 1,1'-azobis(l-phenyl[13C]ethane) (1) at 33°C in benzene. Determination of relative endgroup concentrations in the resulting copolymers allowed determination of the relative rates of addition of MMA and A to the 1-phenylethyl radical derived from 1. We find k~M ^/k A = 0.44 + 0.03, a value consistent with known copolymerization behavior. Further analysis of 75 MHz ~3C NMR spectra led to the determination of kMuA/k A for the 2-(4-phenylpentanenitrile) radical derived from primary radical addition to A. The measured value of kuM A/k A supports only one of five reported studies of the radical copolymerization behavior of MMA and A.
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