Kinetic studies of the copolymerisation of styrene and fluoro-α-methylstyrenes
✍ Scribed by C.A. Barson; D.R. Fenn
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 182 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
Styrene (Mi) has been copolymerised with 14C-labelled fluoro-~-methylstyrenes (M2) in the temperature range 40-105 °, under conditions where [M~]>>[M2]. Arrhenius plots of the values of the reactivity ratio r, indicate that, in the case of 2-fluoro-ct-methylstyrene, the introduction of fluorine considerably reduces monomer activity towards the polystyryl radical compared with ~t-methylstyrene;
both enthalpies and entropies of activation contribute to the reduced activity. In the case of 4-fluoro-~t-methylstyrene, the effect of the fluorine substituent is insignificant. Since neither of the fluoro<t-methylstyrenes homopolymerises, these comonomers do not show the ceiling temperature effects observed with ~t-methylstyrene.
📜 SIMILAR VOLUMES
Kinetics of the copolymerisation of styrene and maleic anhydride have been studied in dioxane at 50 ° using azobisisobutyronitrile as initiator. Explanation of the kinetic behaviour has been attempted in terms of the participation in propagation of a charge-transfer complex between the monomers alon
## Abstract The hydrosilylation reaction of α,ω‐bis(trimethylsiloxy)methylhydridesiloxane to styrene and α‐methylstyrene in the presence of the catalyst platinum hydrochloric acid (a 0.1__M__ solution in tetrahydrofuran) at a 1:35 ratio of initial compounds at various temperatures (80–90°C) was inv