Abstract
AbstractIonic polymerizations of vinylbenzyl methyl ether initiated by either carbanions or Lewis acids has been found to lead to crosslinked polymers. By comparative studies of strong carbanionic bases and Lewis acids with benzyl ethers, it has been possible to define details of mechanisms which in conjunction with cationic or anionic propagation lead to crosslinks. The α‐hydrogens of benzyl ethers have been found to be sufficiently acidic to terminate anionic polymerization of styrene and displacement of alkoxide anion from the benzyl ether linkage by nucelophilic polymer anions is proposed as a mechanism leading to branching and eventual crosslinking in anionic polymerization of vinylbenzyl methyl ether. Cationic polymerization of vinylbenzyl methyl ether is quite complex. In addition to propagation, chain transfer, and spontaneous termination of cation chain carriers, there is evidence for complex formation between Lewis acid initiator and the benzyl ether substituent. A slow decomposition of ether–Lewis acid complexes produces benzylcarbonium ions which alkylate aromatic rings of polymer and thereby crosslink the polymer. Benzyl ether has been found to be an effective chain terminator for cationic styrene polymerization.
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