## Abstract **Summary:** A kinetic study of the polymerization of a mixture of 1,3‐pentadiene isomers initiated by AlCl~3~ was carried out in pentane at −10 and 20 °C. A second apparent monomer order was found mainly at room temperature and was explained by a complexation of propagating active cent
Living cationic polymerization of p-alkoxystyrenes by free ionic species
✍ Scribed by Shokyoku Kanaoka; Toshinobu Higashimura
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 222 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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✦ Synopsis
In contrast to the common view, living cationic polymerization of p-methoxy-and p-t-butoxystyrenes proceeded in polar solvents such as EtNO 2 /CH 2 Cl 2 mixtures, and involvement of free ionic growing species therein was examined. For example, the two alkoxystyrenes were polymerized with the isobutyl vinyl ether-HCl adduct/ZnCl 2 initiating system at Ϫ15°C in such polar solvents as CH 2 Cl 2 or EtNO 2 / CH 2 Cl 2 [1/1 (v/v)], as well as toluene. The number average molecular weight (M n ) of the polymers increased in direct proportion to the monomer conversion, even after sequential monomer addition, and the molecular weight distribution (MWD) stayed very narrow throughout the reaction. In addition, the M n agreed with the calculated values, assuming that one adduct molecule generates one living polymer chain. In these polar media the addition of a common ion salt retarded the polymerization, indicating that dissociated ionic species are involved in the propagating reaction.
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