An Air- and Moisture-stable Zinc(II) Carbene Dithiolate Dimer Showing Fast Thermally Activated Delayed Fluorescence and Dexter Energy Transfer Catalysis.
Ondřej MrózekMousree MitraBejamin HuppAndrey BelyaevNora LüdtkeDorothee WagnerCui WangOliver S WengerChristel M MarianAndreas SteffenPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2023)
A dimeric Zn II carbene complex featuring bridging and chelating benzene-1,2-dithiolate ligands is highly stable towards air and water. The donor-Zn-acceptor structure leads to visible light emission in the solid state, solution and polymer matrices with λ max between 577-657 nm and, for zinc(II) complexes, unusually high radiative rate constants for triplet exciton decay of up to k r =1.5×10 5 s -1 at room temperature. Variable temperature and DFT/MRCI studies show that a small energy gap between the 1/3 LL/LMCT states of only 79 meV is responsible for efficient thermally activated delayed fluorescence (TADF). Time-resolved luminescence and transient absorption studies confirm the occurrence of long-lived, dominantly ligand-to-ligand charge transfer excited states in solution, allowing for application in Dexter energy transfer photocatalysis.