Search

Developing luminescent radicals with tunable emission is a challenging task due to the limitation of alternative skeletons. Herein, a series of carbene‐triphenylamine hybrids were prepared by the direct C2‐arylation of N‐heterocyclic carbenes with 4‐bromo‐N,N‐bis(4‐methoxyphenyl)aniline. These hybrids showed multiple redox‐active properties and could be converted to carbon‐centered luminescent radicals with blue‐to‐cyan emissions (λmax: 436–486 nm) or nitrogen‐centered luminescent radicals with orange emissions (λmax: 590–623 nm) through chemical reduction or oxidation, respectively. The radical species were characterized by electron paramagnetic resonance spectroscopy, ultraviolet‐visible spectroscopy, and single‐crystal X‐ray diffractometry analysis. Notably, the corresponding nitrogen‐centered radicals exhibited good stability in atmospheric air, and their thermal decomposition temperatures were determined to be above 200 °C. In addition, spectral and theoretical calculations indicate that all radicals exhibit anti‐Kasha emissions. [ABSTRACT FROM AUTHOR]