Three NIR-emitting neutral IrIII complexes [Ir(iqbt)2(dpm)] (1), [Ir(iqbt)2(tta)] (2), and [Ir(iqbt)2(dtdk)] (3) based on the 1-(benzo[b]thiophen-2-yl)-isoquinolinate (iqtb) were synthesized and characterized (dpm=2,2,6,6-tetramethyl-3,5-heptanedionate; tta=2-thienoyltrifluoroacetonate; dtdk=1,3-di(thiophen-2-yl)propane-1,3-dionate). The compounds emit between ?=680 and 850 nm with high luminescence quantum yields (up to 16 %). By combining electrochemistry, photophysical measurements, and computational modelling, the relationship between the structure, energy levels, and properties were investigated. NIR-emitting, solution-processed phosphorescent organic light-emitting devices (PHOLEDs) were fabricated using the complexes. The devices show remarkable external quantum efficiencies (above 3 % with 1) with negligible efficiency roll-off values, exceeding the highest reported values for solution-processible NIR emitters.

Near-IR Emitting Iridium(III) Complexes with Heteroaromatic ?-Diketonate Ancillary Ligands for Efficient Solution-Processed OLEDs: Structure-Property Correlations

Marta Penconi;Mariacecilia Pasini;Davide Ceresoli;Clara Baldoli;Umberto Giovanella;Alberto Bossi
2016

Abstract

Three NIR-emitting neutral IrIII complexes [Ir(iqbt)2(dpm)] (1), [Ir(iqbt)2(tta)] (2), and [Ir(iqbt)2(dtdk)] (3) based on the 1-(benzo[b]thiophen-2-yl)-isoquinolinate (iqtb) were synthesized and characterized (dpm=2,2,6,6-tetramethyl-3,5-heptanedionate; tta=2-thienoyltrifluoroacetonate; dtdk=1,3-di(thiophen-2-yl)propane-1,3-dionate). The compounds emit between ?=680 and 850 nm with high luminescence quantum yields (up to 16 %). By combining electrochemistry, photophysical measurements, and computational modelling, the relationship between the structure, energy levels, and properties were investigated. NIR-emitting, solution-processed phosphorescent organic light-emitting devices (PHOLEDs) were fabricated using the complexes. The devices show remarkable external quantum efficiencies (above 3 % with 1) with negligible efficiency roll-off values, exceeding the highest reported values for solution-processible NIR emitters.
2016
Istituto di Scienze e Tecnologie Molecolari - ISTM - Sede Milano
Istituto per lo Studio delle Macromolecole - ISMAC - Sede Milano
density functional calculations · electrochemistry · iridium · organic light emitting diodes · phosphorescence
density functional calculations · electrochemistry · iridium · organic light emitting diodes · phosphorescence
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/309716
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