• Samuel, Ifor David William
• Bansal, Ashu Kumar
• Martínez-Sarti, Laura
• Bolink, Henk J.
• Henwood, Adam Francis
• Slawin, Alexandra Martha Zoya
• Cordes, David Bradford
• Mascio, Vincent Di
• Martir, Diego Rota
• Pertegás, Antonio
• Zysman-Colman, Eli
• Kamer, Paul C. J.

Abstract

Herein we present a structure-property relationship study of thirteen cationic iridium (III) complexes of the form of [Ir(C^N)2(P^P)]PF6 in both solution and the solid state through systematic evaluation of six bisphosphine (P^P) ligands (xantphos, dpephos, dppe, Dppe, nixantphos and isopropxantphos). All of the complexes are sky-blue emissive, but their photoluminescence quantum yield (ΦPL) are generally low. However, strong and long-lived blue luminescence (λem: 471 nm; ΦPL = 52%; τe, of 13.5 μs) can be obtained by combining the reduced bite angle of the 1,2-bis-diphenylphosphinoethene (dppe) chelate with the bulky 2-(4,6-difluorophenyl)-4-mesitylpyridinato (dFmesppy) cyclometalating ligand. To the best of our knowledge this is the highest ΦPL and the longest τe reported for cyclometalated iridium(III) complexes bearing bisphosphine ligands. Light-emitting electrochemical cells (LEECs) were fabricated using lead complexes from this study, however due in part to the irreversible electrochemistry, no functional LEEC was achieved. Organic light-emitting diodes were successfully fabricated but only attained maximum external quantum efficiencies of 0.25%.

Topics

• impedance spectroscopy
• photoluminescence
• Iridium