Highly Emissive Fused Heterocyclic Alkynylgold(III) Complexes for Multiple Color Emission Spanning from Green to Red for Solution‐Processable Organic Light‐Emitting Devices
A new class of fused heterocyclic tridentate ligand‐containing alkynylgold(III) complexes with tunable emission color has been successfully designed and synthesized. Structural modification of the σ‐donating fused heterocyclic alkynyl ligands, including substituted fluorene, carbazole, and triphenyl...
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Veröffentlicht in: | Angewandte Chemie International Edition 2018-05, Vol.57 (19), p.5463-5466 |
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Sprache: | eng |
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Zusammenfassung: | A new class of fused heterocyclic tridentate ligand‐containing alkynylgold(III) complexes with tunable emission color has been successfully designed and synthesized. Structural modification of the σ‐donating fused heterocyclic alkynyl ligands, including substituted fluorene, carbazole, and triphenylamine, enables a large spectral shift of about 110 nm (ca. 3310 cm−1) that covers the green to red region to be realized with the same tridentate ligand‐containing alkynylgold(III) complexes in solid‐state thin films. Interestingly, the energy of the excimeric emission can be controlled by the rational design of the fused heterocyclic alkynyl ligands. Superior solution‐processable organic light‐emitting devices (OLEDs) with high external quantum efficiencies (EQEs) of 12.2, 13.5, 9.3, and 5.2 % were obtained with green, yellow, orange, and red emission. These high EQE values are comparable to those of the vacuum‐deposited OLEDs based on structurally related alkynylgold(III) complexes.
Calling the tune: A novel class of fused heterocyclic alkynylgold(III) complexes has been successfully designed and synthesized. Through careful choice of the σ‐donating fused heterocyclic alkynyl ligands, the emission energy can be effectively controlled and fine‐tuned from green to red. In addition, superior solution‐processable OLEDs with high external quantum efficiencies of up to 13.5 % can be realized. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.201711846 |