The control of hydroxylated polyethylene (PE) structures was investigated in the copolymerization of ethylene with allyl alcohol or 10‐undecen‐1‐ol with a specific metallocene, methylaluminoxane, and trialkyl aluminum catalyst system through changes in the copolymerization conditions. The incorporation of allyl alcohol into the PE backbones was controllable through changes in the trialkyl aluminum, leading to terminally hydroxylated PE or a copolymer possessing hydroxyalkyl side chains. The copolymerization of ethylene with 10‐undecen‐1‐ol gave copolymers with hydroxyalkyl side chains of various contents with a variety of molecular weights through changes in the copolymerization conditions. The obtained copolymers were useful as macroinitiators that allowed polar polymer segments to grow on the PE backbones, leading to the creation of graft copolymers that possessed PE and polar polymer segments. In this way, polyethylene‐g‐poly(propylene glycol) (PE‐g‐PPG) and polyethylene‐g‐poly(ϵ‐caprolactone) (PE‐g‐PCL) were synthesized. The 13C NMR analysis of PE‐g‐PPG suggested that all the hydroxyl groups were consumed for propylene oxide polymerization, and transmission electron microscopy demonstrated nanoorder phase separation and indistinct phase boundaries. 13C NMR and gel permeation chromatography analyses indicated the formation of PE‐g‐PCL, in which 36–80 mol % of the hydroxyl groups worked as initiators for ϵ‐caprolactone polymerization.
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Kashiwa et al. (2003) studied this question.