2022
DOI: 10.1002/anie.202209451
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Au⋅⋅⋅H−C Interactions Support a Robust Thermally Activated Delayed Fluorescence (TADF) Gold(I) Complex for OLEDs with Little Efficiency Roll‐Off and Good Stability

Abstract: The practical use of luminescent mononuclear gold(I) complexes as optoelectronic materials has been limited by their inferior stability. Herein we demonstrate a strategy to improve the stability of gold(I) complexes which display thermally activated delayed fluorescence (TADF). A highly rigid and groove‐like σ‐donating aryl ligand has been used to form dual Au⋅⋅⋅H−C hydrogen bonds. The secondary metal‐ligand interactions have been authenticated by single‐crystal structure, NMR spectroscopy and theoretical simu… Show more

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Cited by 34 publications
(32 citation statements)
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“…Comparing with Pt( ii ) complexes supported by tetradentate ligands which have been highly sought after because of the chelating effect of ligands, 15 the leveraging of intramolecular noncovalent interactions suggests a promising way to robust emitters. 16…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Comparing with Pt( ii ) complexes supported by tetradentate ligands which have been highly sought after because of the chelating effect of ligands, 15 the leveraging of intramolecular noncovalent interactions suggests a promising way to robust emitters. 16…”
Section: Resultsmentioning
confidence: 99%
“…Comparing with Pt(II) complexes supported by tetradentate ligands which have been highly sought after because of the chelating effect of ligands, 15 the leveraging of intramolecular noncovalent interactions suggests a promising way to robust emitters. 16 To acquire the structural parameters which are key to 3 MMLCT emission properties, single crystals of all the four complexes were grown for X-ray diffraction studies. Full crystallographic information in CIF format has been deposited at the Cambridge Crystallographic Data Center (CCDC †) under deposition numbers 2209083, 2209084, 2209085 and 2209086 for Pt-1, Pt-2, Pt-3 and Pt-4, respectively.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…1.97–1.98 Å for carbene–Au–amide) has been ascribed to the stronger trans ‐effect of the aryl ligand. [ 50 ] DCzBN–Au has a slightly bent coordination geometry (C NHC AuC aryl bond angle: 172.98°), presumably due to the crystallization effect. The carbene motif is twisted with respect to the BN plane with a dihedral angle of ≈20°, revealing its tendency to have a co‐planar orientation akin to previous findings on carbene–Au–L (L = ligand) complexes devoid of steric hindrance between the two ligands.…”
Section: Resultsmentioning
confidence: 99%
“…Such depressed non-radiative decay was also observed in some recent TADF CMAs with orthogonal geometry. [30,31] For completeness, the even higher k nr in Cu2 and Cu3 than Cu1 and Cu4 can be blamed to additional energy losses via free motions of alkyl substituents.…”
Section: Zuschriftenmentioning
confidence: 99%