1. Polyolefin–Polar Block Copolymers from Versatile New Macromonomers
- Author
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Tony McNally, Carl Waterson, Christopher Kay, Colin Morton, Peter Scott, Shaun Morris, Kenneth Lewtas, Connah A. Burnett, Peter M. Wright, Paul D. Goring, Ben Hornby, and Giles W. Theaker
- Subjects
TP ,Acrylate ,010405 organic chemistry ,Hydride ,General Chemistry ,010402 general chemistry ,Macromonomer ,01 natural sciences ,Biochemistry ,Catalysis ,0104 chemical sciences ,Polyolefin ,chemistry.chemical_compound ,End-group ,Colloid and Surface Chemistry ,Monomer ,chemistry ,Polymerization ,Polymer chemistry ,Copolymer - Abstract
A new metallocene-based polymerization mechanism is elucidated in which a zirconium hydride center inserts α-methylstyrene at the start of a polymer chain. The hydride is then regenerated by hydrogenation to release a polyolefin containing a single terminal α-methylstyrenyl group. Through the use of the difunctional monomer 1,3-diisopropenylbenzene, this catalytic hydride insertion polymerization is applied to the production of linear polyethylene and ethylene-hexene copolymers containing an isopropenylbenzene end group. Conducting simple radical polymerizations in the presence of this new type of macromonomer leads to diblock copolymers containing a polyolefin attached to an acrylate, methacrylate, vinyl ester, or styrenic segments. The new materials are readily available and exhibit interfacial phenomena, including the mediation of the mixing of immiscible polymer blends.
- Published
- 2018
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