TY - JOUR
T1 - Molecular Engineering of Iridium Blue Emitters Using Aryl N-Heterocyclic Carbene Ligands
AU - Aghazada, Sadig
AU - Huckaba, Aron J.
AU - Pertegas, Antonio
AU - Babaei, Azin
AU - Grancini, Giulia
AU - Zimmermann, Iwan
AU - Bolink, Henk
AU - Nazeeruddin, Mohammad Khaja
N1 - Publisher Copyright:
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2016/11
Y1 - 2016/11
N2 - The synthesis of a new series of neutral bis[2-(2′,4′-difluorophen-2′-yl)pyridine][1-(2′-aryl)-3-methylimidazol-2-ylidene]iridium(III) complexes is reported. Each complex has been characterized by NMR spectroscopy, UV/Vis spectrophotometry, and cyclic voltammetry, and the photophysical properties examined in depth. Furthermore, two of the complexes have been characterized by single-crystal X-ray diffraction analysis. By systematically modifying the cyclometalating aryl group on the N-heterocyclic carbene (NHC) ligand from 2,4-dimethoxyphenyl to 6-methoxy-2-methyl-3-pyridyl, the energy levels of the Ir complexes were modified to produce new blue emitters with increased HOMO and triplet-state energies. OLED devices fabricated with these emitters showed external quantum efficiencies (EQEs) in the range of 2.3–3.2 % with low turn-on values of 2.7–2.9 V and efficacies of up to 6.3 %.
AB - The synthesis of a new series of neutral bis[2-(2′,4′-difluorophen-2′-yl)pyridine][1-(2′-aryl)-3-methylimidazol-2-ylidene]iridium(III) complexes is reported. Each complex has been characterized by NMR spectroscopy, UV/Vis spectrophotometry, and cyclic voltammetry, and the photophysical properties examined in depth. Furthermore, two of the complexes have been characterized by single-crystal X-ray diffraction analysis. By systematically modifying the cyclometalating aryl group on the N-heterocyclic carbene (NHC) ligand from 2,4-dimethoxyphenyl to 6-methoxy-2-methyl-3-pyridyl, the energy levels of the Ir complexes were modified to produce new blue emitters with increased HOMO and triplet-state energies. OLED devices fabricated with these emitters showed external quantum efficiencies (EQEs) in the range of 2.3–3.2 % with low turn-on values of 2.7–2.9 V and efficacies of up to 6.3 %.
KW - Carbenes
KW - Iridium
KW - Luminescence
KW - Nitrogen heterocycles
KW - Organic light-emitting diodes
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U2 - 10.1002/ejic.201600971
DO - 10.1002/ejic.201600971
M3 - Article
AN - SCOPUS:84991075819
SN - 1434-1948
VL - 2016
SP - 5089
EP - 5097
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 32
ER -