Bright, Modular, and Switchable Near-Infrared II Emission from Compact Tetrathiafulvalene-Based Diradicaloid Complexes

• Published in: Journal of the American Chemical Society 2022-09, Vol.144 (36), p.16447-16455
• Main Authors: McNamara, Lauren E., Boyn, Jan-Niklas, Melnychuk, Christopher, Anferov, Sophie W., Mazziotti, David A., Schaller, Richard D., Anderson, John S.
• Format: Article
• Language: English
• Subjects: INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.2c04976

Near-infrared (NIR)-emitting molecules are promising candidates for biological sensing and imaging applications; however, many NIR dyes are large conjugated systems which frequently have issues with stability, solubility, and tunability. Here, we report a novel class of compact and tunable fluorescent diradicaloid complexes which are air-, water-, light-, and temperature-stable. These properties arise from a compressed π manifold which promotes an intense ligand-centered π–π transition in the NIR II (1000–1700 nm) region and which subsequently emits at ∼1200 nm. This emission is among the brightest known for monomolecular lumiphores with deep NIR II (>1100 nm) emission, nearly an order of magnitude brighter than the commercially available NIR II dye IR 26. Furthermore, this fluorescence is electrochemically sensitive, with efficient switching upon addition of redox agents. The brightness, stability, and modularity of this system distinguish it as a promising candidate for the development of new technologies built around NIR emission.