Syntheses, photoluminescence and electroluminescence of some new blue-emitting phosphorescent iridium(III)-based materials

Inamur R. Laskar, Shih Feng Hsu, Teng-Ming Chen*

*Corresponding author for this work

Research output: Contribution to journalArticle

71 Scopus citations


The cyclometallated ligand 2-(4′,6-difluorophenyl)-4-methoxypyridine (F2MeOppyH), whose complexes with iridium(III) emit bright blue to green light, was synthesized in five separate steps. Ir(F2MeOppy) 2(acac), (acacH = 2,4-pentanedione), Ir(F2MeOppy) 2(pic) (picH = 2-picolinic acid), fac-Ir(F2MeOppy) 3 and mer-Ir(F2MeOppy)3 complexes were synthesized from solution and fully characterized. The structures of Ir(F 2MeOppy)2(acac) and fac-Ir(F2MeOppy) 3 were authenticated by X-ray single crystal structure analysis. fac-Ir(F2MeOppy)3 showed a much higher solution photoluminescence (PL) quantum efficiency and blue-shifted emission compared to its counter mer-isomer. All of the complexes showed reversible oxidations between 0.3 and 0.7 V versus the ferrocene/ferrocenium ion. The relative thermodynamic stability of the mer versus fac isomer was investigated and correlated to their corresponding redox and PL properties. Two electroluminescent (EL) devices (D-1 and D-2) were fabricated using the same blue Ir(F2MeOppy)2(acac) complex as a a dopant but with two different hole blockers, BCP and BAlq, and consequently BCP proved itself a good hole blocker for this type of system. The fabrication of another EL device (D-3) was carried out by using the same dopant, only replacing the host CBP by a wider band gap host, mCP which showed improved luminance, luminance yield and power efficiency (D-2: 133 cd m-2, 0.66 cd A-1, 0.22 lm W-1; D-3: 326 cd m-2; 1.63 cd A-1; 0.26 lm W-1).

Original languageEnglish
Pages (from-to)189-200
Number of pages12
Issue number2
StatePublished - 27 Jan 2005


  • Blue phosphorescent
  • Electroluminescence
  • Facial
  • Iridium(III) complex
  • Meridional
  • Photoluminescence

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