Abstract
4-Substituted styrenes (substituent: methoxy, methyl, acetoxy, maleimido and none), were cationically polymerized with an initiator system involving poly( p-maleimidostyrene)(PMS) as a macroinitiator, having highly reactive pendent maleimide moieties and a α-chlorobenzyl structure at the polymer end. Using PMS/SnCl 4/tetra- n-butylammmonium chloride initiator system, block copolymers of 4-substituted styrenes onto PMS were obtained in CH 2Cl 2 at 0 °C. As for the polymerization of N-(4-vinylphenyl)maleimide and 4-acetoxystyrene, especially, PMS as the macroinitiator was almost completely utilized for initiation reaction and the polymers having PMS- b-poly(4-substituted styrene) platform with very narrow and unimodal molecular weight distribution were formed in contrast with the case of using 4-methoxystyrene and 4-methylstyrene with stronger electron releasing groups, in which the molecular weight distributions of the formed polymeric materials appeared to be bimodal.
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