Journal
ADVANCED FUNCTIONAL MATERIALS
Volume 30, Issue 25, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202002494
Keywords
near-infrared phosphorescent emitters; organic light-emitting diodes; Pt(II) complexes; solid-state aggregation; trimers
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Funding
- Ministry of Science and Technology (MOST)
- National Key R&D Program of China [2016YFB0401002]
- Science Achievement Scholarship of Thailand (SAST)
- Chiang Mai University
- Internal Funds KU Leuven
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The design of square-planar Pt(II) complexes with highly efficient solid-state near infrared (NIR) luminescence for electroluminescence is attractive but challenging. This study presents the fine-turning of excited-state properties and application of a series of isoquinolinyl pyrazolate Pt(II) complexes that are modulated by steric demanding substituents. It reveals that the bulky substituents do not always disfavor metallophilic Pt center dot center dot center dot Pt interactions. Instead, pi-pi stacking among chelates, which are fine-tuned by the associated substituents, also exerts strong influence to the metal-metal-to-ligand charge transfer (MMLCT) transition character. Theoretical calculations indicate that Pt center dot center dot center dot Pt contacts become more relevant in the trimers rather than the dimers, especially in their T-1 states, associated with a change from mixed (LC)-L-3/(MLCT)-M-3 transition in the monomer/dimer to mixed (LC)-L-3/(MMLCT)-M-3 transition character in the trimer. Electroluminescence devices affording intense deep-red/NIR emission (near 670 nm) with unprecedentedly high external quantum efficiency over 30% are demonstrated. This work provides deep insights into formation MMLCT transition of square-planar Pt(II) complexes and efficient molecular design for deep-red/NIR electroluminescence.
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