This paper describes a novel route to prepare polypropylene diblock co
polymers, such as PP-b-PMMA, which comprise a polypropylene and free r
adical polymerized polymer segment. The chemistry involves a transform
ation process from metallocene catalysis to borane chemistry. Firstly,
polypropylene with chain end unsaturation was prepared by metallocene
catalysts, such as Et(Ind)(2)ZrCl2/MAO. Secondly, the olefinic chain
end was hydroborated by 9-BBN to produce borane terminated PP. Thirdly
, the borane group at the chain end was selectively oxidized and inter
converted to polymeric radical which then initiated radical polymeriza
tion to produce diblock copolymers. Despite the heterogeneous reaction
conditions, the overall yield and structure of diblock copolymers are
quite satisfactory. In addition, the chain extension process, showing
no significant broading in molecular weight distribution, implies a '
stable' radical polymerization. (C) 1997 Elsevier Science Ltd.