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The Copolymerization of the Vinyl Monomer with a Cyclic Compound. III. The Cationic Copolymerization of Styrene with Substituted Ethylene Oxides

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TLDR
In this article, the copolymerization of styrene with substituted ethylene oxides catalyzed by boron trifluoride - diethyl ether has been investigated.
Abstract
The copolymerization of styrene with substituted ethylene oxides catalyzed by boron trifluoride - diethyl ether has been investigated. In all cases, rather low-molecular-weight copolymers were obtained. The copolymerization reactivity of the substituted ethylene oxides with styrene varied with the substituents, in the order of: isobutene oxide>propylene oxide>styrene oxide>epichlorohydrin. This has been explained in terms of cross-propagation or the reaction of the growing oxide cation with styrene. The styrene unit content of the copolymer of styrene and epichlorohydrin increases with an increase in the solvent polarity and with an increase in the temperature. It has been concluded from the experimental results that the copolymerizability of alkylene oxide toward styrene is increased by the introduction of electron-releasing substituents into the oxide and by the use of a polar solvent at a moderate temperature.

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Citations
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Cationic copolymerization behavior of epoxide and 3‐isochromanone

TL;DR: Cationic copolymerization of n-butyl glycidyl ether (BGE) and 3-isochromanone (ICM) was investigated using trifluoromethanesulfonic acid (TfOH) as an initiator at 100 °C.
Journal ArticleDOI

Cationic Copolymerization of Styrene Derivatives and Oxiranes via Concurrent Vinyl-Addition and Ring-Opening Mechanisms: Multiblock Copolymer Formation via Occasional Crossover Reactions

TL;DR: In this paper, Strene derivatives were demonstrated to copolymerize with 2,2-disubstituted oxiranes, which can generate a tertiary carbocation by the ring opening of the oxonium ion, through crossov
References
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Journal ArticleDOI

The Copolymerization of the Vinyl Monomer with a Cyclic Compound. I. The Cationic Copolymerization of Some Vinyl Monomers with 3,3-Bis (chloromethyl) oxetane

TL;DR: In this article, the copolymerization of several vinyl monomers, such as styrene, α-methylstyrene and isobutyl vinyl ether, with 3,3-bis(chloromethyl)oxetane catalyzed by Lewis acids (boron trifluoride-diethyl etherate, stannic chloride and triethylaluminum-water) in methylene chloride at 0°C has been investigated.
Journal ArticleDOI

The Copolymerization of the Vinyl Monomer with a Cyclic Compound. II. The Cationic Copolymerization of Some Vinyl Monomers with β-Propiolactone

TL;DR: In this article, the copolymerization of several vinyl monomers, such as styrene (St), α-methylstyrene and isobutyl vinyl ether, with β-propiolactone (β-PL) as catalyzed by Lewis acids has been investigated in methylene chloride at 0°C.
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