Abstract: | A series of soluble, conjugated, electrophosphorescent copolymers with (meso‐tetraphenylporphyrinato‐κ4N)platinum(II) (PtTPP) complexes incorporated into the polymer main chain were synthesized through the copolymerization of narrow‐band‐gap monomeric porphyrin–platinum(II) complexes and wide‐band‐gap dialkyl‐substituted fluorene monomers by a modified Suzuki coupling reaction. The study of the photoluminescence decay indicated that poly2,7‐(9,9‐dioctylfluorene)‐co‐2,12‐((meso‐tetraphenylporphyrinato‐κ4N)platinum(II))] (PFO–PtTPP) was a triplet emitter. The electroluminescence emission from the fluorene segment was completely quenched for copolymers with PtTPP contents as low as 0.5 mol %. The PFO–PtTPP copolymers emitted deep red light. The device based on the porphyrin–platinum(II) copolymer PFO–5PtTPP (with 5 mol % PtTPP in the copolymer) showed the highest external quantum efficiency of 1.95% with an emission peak at 684 nm in an indium tin oxide/poly(3,4‐ethylenedioxythiophene)/polyvinylcarbazole (PVK)/70:30 (w/w) PFO–5PtTPP: 2‐(biphenyl‐4‐yl)‐5‐(4‐tert‐butylphenyl)‐1,3,4‐oxadiazole/Ba/Al device configuration. In comparison with the PFO–PtTPP copolymers synthesized via a postpolymerization metalation route, copolymerization from Pt metal complexes proved to be a more efficient synthetic route for high‐efficiency electrophosphorescent polymers. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 4174–4186, 2006 |