A new class of cyclometalated tetradentate alkynylgold(III) complexes has been successfully synthesized by post-synthetic modification. Through the judicious design and choice of pincer ligands, post-synthetic cyclization could be achieved to produce the robust and structurally rigid class of tetradentate gold(III) C^N^C^C complexes with high photoluminescence quantum yields of up to 0.49 in solution and 0.78 in doped thin films at room temperature, at least an order of magnitude higher than those of the structurally related uncyclized tridentate alkynylgold(III) analogues. High-performance yellow to orange-red emitting solution-processable organic light-emitting devices have also been achieved with external quantum efficiency of 11.1 %. This work describes for the first time of the use of post-synthetic ligand modification approach to overcome the synthetic challenge for tetradentate alkynylgold(III) complexes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.201607816 | DOI Listing |
Angew Chem Int Ed Engl
December 2023
Key Laboratory of Applied Surface and Colloid Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an, 710119, P. R. China.
Condensed films of functional luminophores dominated by the magnitude and dimensionality of the intermolecular interactions play important roles in sensing performance. However, controlling the molecular assembly and regulating photophysical properties remain challenging. In this study, a new luminophore, ortho-PBI-Au, was synthesized by anchoring a cyclometalated alkynyl-gold(III) unit at the ortho-position of perylene bisimide.
View Article and Find Full Text PDFChem Sci
July 2021
Institute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong Pokfulam Road Hong Kong P. R. China +86-852-2857-1586 +86-852-2859-2153.
Here, we report the design and synthesis of a new class of fused heterocyclic alkynyl ligand-containing gold(iii) complexes, which show tunable emission colors spanning from the yellow to red region in the solid state and exhibit thermally activated delayed fluorescence (TADF) properties. These complexes display high photoluminescence quantum yields of up to 0.87 and short excited-state lifetimes in sub-microsecond timescales, yielding high radiative decay rate constants on the order of up to 10 s.
View Article and Find Full Text PDFACS Appl Mater Interfaces
February 2021
Key Laboratory of Applied Surface and Colloid Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710062, P. R. China.
Development of high-performance, low-power-consumption, small-sized detectors is a key issue for fabricating specific miniaturized chromatographs (GCs). Herein, we report, for the first-time, utilization of a film-based fluorescent sensor as a GC detector. In the studies, we designed a new -carborane derivative of a known cyclometalated alkynyl-gold(III) complex, .
View Article and Find Full Text PDFChem Commun (Camb)
November 2019
Institute of Molecular Functional Materials [Areas of Excellence Scheme, University Grants Committee (Hong Kong)] and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.
Bipolar cyclometalated dendritic alkynylgold(iii) complexes that exhibit excellent film morphologies in solid-state thin films have been designed and synthesized. Together with their high luminescence quantum yields, high performance solution-processable organic light-emitting devices have been realized, maintaining high external quantum efficiencies of >12% for dendrimers up to the second generation.
View Article and Find Full Text PDFThermally stable, strongly luminescent gold-TADF emitters are the clue to realize practical applications of gold metal in next generation display and lighting technology, a scarce example of which is herein described. A series of donor-acceptor type cyclometalated gold(III) alkynyl complexes with some of them displaying highly efficient thermally activated delayed fluorescence (TADF) with Φ up to 88% in thin films and emission lifetimes of ≈1-2 µs at room temperature are developed. The emission color of these complexes is readily tunable from green to red by varying the donor unit and cyclometalating ligand.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!