Abstract
Metallocene-catalyzed propylene–ethylene copolymer (PER) having a terminal vinylidene group, reacted with maleic anhydride without free radical conditions to prepare terminally MAH-functionalized PER. Through the analysis of the obtained polymer by 13C NMR spectroscopy, it was shown that a large part of a terminal vinylidene group isomerizes to a more stable internal double bond in this reaction and that the PER–MAH is formed via the reaction of MAH with isomerized PER and original PER.
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