Hyperbranched polyethers with tunable glass transition temperature: controlled synthesis and mixing rules

By taking advantage of competing side reactions, controlled synthesis of a series of homo- and co-polymerized hyperbranched polyethers (HBPEs) is demonstrated using AB(2) monomers of different spacer lengths. This reacting system shows good controllability and scalability. More importantly, the degree of branching is found to be insensitive to the molecular weight and spacer length in monomers. Thus, the value and width of T-g can be tuned by varying monomer spacer length, terminal groups, molecular weight, as well as by copolymerization and physical blending. The dependence of T-g in binary homopolymer blends on composition and the dependence of T-g in copolymers on monomer ratio are established and compared for the first time. T-g of copolymers obeys the Fox equation, whereas T-g in binary blends only follows the Kwei equation. Copolymerization does not increase the width of T-g. In contrast, the width of T-g of binary blends is much broader than that of copolymers, even though the broadening in T-g can be reduced by increasing the polarity of terminal groups.