PhosphorescentDinuclear Pd–Pd Emitters inOLED Applications

Four phosphorescent dinuclear Pd–Pd complexes were synthesized by using the clamping ligand <i>N</i>,<i>N</i>′-diphenylformamidine and primary ligands of C∧N, which both have high ligand field strength to enhance the luminescence of the complexes. The single-crystal data confirmed their clamshell structures and revealed Pd–Pd distances between 2.829 and 2.864 Å. In addition, time-dependent density functional theory calculations revealed the phosphorescent nature of the metal–metal-to-ligand charge transfer and ligand-to-ligand charge transfer in these complexes. Moreover, complexes <b>3</b> and <b>4</b> were used to fabricate an OLED by a vapor phase deposition technique. At an optimal doping concentration of 5%, the <b>3</b>-based device showed a maximum external quantum efficiency (EQE<sub>max</sub>) of 8.79% for CIE coordinates of (0.49, 0.48) and the <b>4</b>-based device showed an EQE<sub>max</sub> of 13.10% for CIE coordinates of (0.61, 0.37).

Publication Details

Journal
Figshare
Published
2025-02-13
DOI
https://doi.org/10.1021/acs.inorgchem.4c02929.s001
Primary Topic
Organic Light-Emitting Diodes Research
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article
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PhosphorescentDinuclear Pd–Pd Emitters inOLED Applications

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Organic Light-Emitting Diodes Research
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PhosphorescentDinuclear Pd–Pd Emitters inOLED Applications

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Abstract

Four phosphorescent dinuclear Pd–Pd complexes were synthesized by using the clamping ligand <i>N</i>,<i>N</i>′-diphenylformamidine and primary ligands of C∧N, which both have high ligand field strength to enhance the luminescence of the complexes. The single-crystal data confirmed their clamshell structures and revealed Pd–Pd distances between 2.829 and 2.864 Å. In addition, time-dependent density functional theory calculations revealed the phosphorescent nature of the metal–metal-to-ligand charge transfer and ligand-to-ligand charge transfer in these complexes. Moreover, complexes <b>3</b> and <b>4</b> were used to fabricate an OLED by a vapor phase deposition technique. At an optimal doping concentration of 5%, the <b>3</b>-based device showed a maximum external quantum efficiency (EQE<sub>max</sub>) of 8.79% for CIE coordinates of (0.49, 0.48) and the <b>4</b>-based device showed an EQE<sub>max</sub> of 13.10% for CIE coordinates of (0.61, 0.37).

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