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A Simple Molecular Design Strategy for Delayed Fluorescence Toward 1000 Nm

Overview
Journal J Am Chem Soc
Specialty Chemistry
Date 2019 Oct 30
PMID 31661267
Citations 20
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Abstract

Harnessing the near-infrared (NIR) region of the electromagnetic spectrum is exceedingly important for photovoltaics, telecommunications, and the biomedical sciences. While thermally activated delayed fluorescent (TADF) materials have attracted much interest due to their intense luminescence and narrow exchange energies (Δ), they are still greatly inferior to conventional fluorescent dyes in the NIR, which precludes their application. This is because securing a sufficiently strong donor-acceptor (D-A) interaction for NIR emission alongside the narrow Δ required for TADF is highly challenging. Here, we demonstrate that by abandoning the common polydonor model in favor of a D-A dyad structure, a sufficiently strong D-A interaction can be obtained to realize a TADF emitter capable of photoluminescence (PL) close to 1000 nm. Electroluminescence (EL) at a peak wavelength of 904 nm is also reported. This strategy is both conceptually and synthetically simple and offers a new approach to the development of future NIR TADF materials.

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References
1.
Xue J, Liang Q, Wang R, Hou J, Li W, Peng Q . Highly Efficient Thermally Activated Delayed Fluorescence via J-Aggregates with Strong Intermolecular Charge Transfer. Adv Mater. 2019; 31(28):e1808242. DOI: 10.1002/adma.201808242. View

2.
Lei Z, Sun C, Pei P, Wang S, Li D, Zhang X . Stable, Wavelength-Tunable Fluorescent Dyes in the NIR-II Region for In Vivo High-Contrast Bioimaging and Multiplexed Biosensing. Angew Chem Int Ed Engl. 2019; 58(24):8166-8171. DOI: 10.1002/anie.201904182. View

3.
Tsujimoto H, Ha D, Markopoulos G, Chae H, Baldo M, Swager T . Thermally Activated Delayed Fluorescence and Aggregation Induced Emission with Through-Space Charge Transfer. J Am Chem Soc. 2017; 139(13):4894-4900. DOI: 10.1021/jacs.7b00873. View

4.
Li C, Duan R, Liang B, Han G, Wang S, Ye K . Deep-Red to Near-Infrared Thermally Activated Delayed Fluorescence in Organic Solid Films and Electroluminescent Devices. Angew Chem Int Ed Engl. 2017; 56(38):11525-11529. DOI: 10.1002/anie.201706464. View

5.
Moral M, Muccioli L, Son W, Olivier Y, Sancho-Garcia J . Theoretical rationalization of the singlet-triplet gap in OLEDs materials: impact of charge-transfer character. J Chem Theory Comput. 2015; 11(1):168-77. DOI: 10.1021/ct500957s. View