Thermally activated delayed fluorescence (TADF) from linear two-coordinate coinage metal complexes is sensitive to the geometric arrangement of the ligands. Herein we realize the tuning of configuration from coplanar to orthogonal gradually by variation of substituents. In a complex with confined twist configuration, its blue emission peaking at 458 nm presents a high Φ of 0.74 and a short τ of 1.9 μs, which indicates a fast enough k of 3.9×10 s and a depressed k of 1.4×10 s . Such outstanding luminescent properties are attributed to the proper overlap of HOMO and LUMO on Cu d orbitals that guarantees not only small ΔE but also sufficient transition oscillator strength for fast . Vacuum-deposited blue OLEDs with either doped or host-free emissive layer present external quantum efficiencies over 20 % and 10 %, respectively, demonstrating the practicality of the configurationally confined strategy for efficient linear Cu TADF emitters.
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http://dx.doi.org/10.1002/anie.202217195 | DOI Listing |
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