Synthesis and characterization of alternating copolymers of fluorene and oxadiazole

Alternating copolymers of 9,9-dioctylfluorene and oxadiazole have been prepared by the tetrazole route or the Suzuki coupling reaction. In the polymers the oxadiazole units were evenly dispersed in the main chain at every one, P(F-1-alt-Ox), three, P(F-3-alt-Ox), or four, P(F-4-alt-OX), fluorene units. Another copolymer with an asymmetric repeat unit structure, P(F-3-Ox-F-1-Ox) has also been prepared for comparison. In this study, the tetrazole route has been demonstrated to offer several advantages for preparing polyoxadiazole with well-defined structures compared to other oxadiazole ring formation reactions. These advantages include: clean and fast reactions, mild reaction conditions, high yields, and high molecular masses of product. The glass transition temperature of copolymers ranged from 98 to 150 degreesC, and the copolymers show high thermal stability with decomposition temperatures around 430 degreesC. The UV-vis absorption and photoluminescence properties of all the copolymers in solutions are similar to those of poly(9,9-dioctylfluorene). All copolymers fluoresce in the blue-light range with quantum yields of similar to70% in CH2Cl2 solution.