Abstract
Apparent reactivity ratios and detailed NMR analysis of copolymerizations of eight membered ring-opening allylic sulfide monomers; 3-methylene-1,5-oxathiocan-2-one 2 and 2,2,4-trimethyl-7-methylene-1,5-dithiocane 5 with methyl methacrylate and styrene are presented. The activated double bond of 2 and unactivated double bond and additional methyl substituents of 5 were found to have a profound affect on reactivity. The copolymerization rates were analyzed based on the lumped parameter kp(f/kt)0.5, which was estimated as a function of monomer composition in the feed.
| Original language | English |
|---|---|
| Pages (from-to) | 2475-2485 |
| Number of pages | 11 |
| Journal | European Polymer Journal |
| Volume | 42 |
| Issue number | 10 |
| Early online date | 12 Jun 2006 |
| DOIs | |
| Publication status | Published - Oct 2006 |
| Externally published | Yes |
Keywords
- Copolymerization
- Free radical
- Ring-opening
- Sulfanyl radical
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