Add time:08/23/2019         Source:sciencedirect.com

We prepared three new poly(9,9-dihexylfluorene) derivatives (P1–P3) containing kinked aromatic triazole (triphenyl-1,2,4-triazole derivative) via Suzuki coupling polymerization. These copolymers were soluble in common organic solvents and showed high decomposition temperatures (Td = 416–454 °C). The optical and electrochemical properties of P1–P3 were compared with poly(9,9-dihexylfluorene) (PFO) and P4 and P5 in which the linkages of the aromatic triazole were different. After introducing the triazole units, absorption spectra showed blue shift (388 nm → 372 nm) due to reduced conjugation, but PL spectra remained almost unchanged (417–418 nm). The linkages of triazole with fluorene segments in P1–P5 were different: (1) fluorene segments linked with triazole through a kinked angle (P1 and P2), (2) triazole as a branch unit (P3) and as terminal groups (P4), (3) fluorene segments linked with triazole in a linear way (P5). As estimated from semi-empirical MNDO calculation, two twisted conformations (ca. 90° each) exist between triazole core and fluorene groups. These kinked conformation and twisted structure increased the PL efficiency (ΦPL = 0.60–0.73, ΦPL = 0.58 for PFO) and partially inhibited annealing-induced excimer formation. From cyclic voltammetric results, P1–P3 exhibited better electron affinity (LUMO: −2.75 to −2.82 eV) than PFO (LUMO: −2.52 eV).

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