A series of vinyl copolymers (PVKST12-PVKST91) and homoploymer PVST containing pendant hole-transporting 4-(4-oxystyryl)triphenylamine (12-100 mol%) and carbazole chromophores were synthesized by radical copolymerization and employed as host for Ir(ppy)(3) phosphor to tune emission color. They were characterized using the H-1 NMR, FT-IR, absorption and photoluminescence spectra, elemental analysis, GPC, cyclic voltammetric and thermal analysis (DSC, TGA). Their weight-average molecular weights (M-w) and decomposition temperatures (T-d) were 1.46-5.68 x 10(4) and 356-399 degrees C, respectively. The HOMO levels of PVKST12-PVKST91 and PVST estimated from the onset oxidation potentials in cyclic voltammograms, were -5.40 to -5.14 eV, which are much higher than -5.8 eV of the conventional host poly(9-vinylcarbazole) (PVK) owing to high hole-affinity of the 4-(4-oxystyryl)triphenylamine groups. Therefore, copolymers PVKST are effective in reducing hole-injection barrier between the PEDOT:PSS and emitting layer. Electroluminescent devices [ITO/PEDOT:PSS/PVKST:Ir(ppy)(3):PBD/BCP/Ca/Al] using the hole-transporting PVKST as host were fabricated to tune the emission color. Their EL spectra showed a major emission at 515 nm and a minor peak at 435 nm attributed to Ir(ppy)(3) and 4-(4-oxystyryl)triphenylamine, respectively. The C.I.E. 1931 coordinates shift from (0.29, 0.61) for PVK to (0.33, 0.42) for PVST with an increase in 4-(4-oxystyryl)triphenylamine content. (C) 2008 Elsevier Ltd. All rights reserved.