Abstract
In this work, we present for the first time a general strategy via molecular reversed conformational distortion for thermally activated delayed fluorescence (TADF). A model purely organic compound named BNNIO with a common fluorophore flexibly linked to benzene by an oxygen atom is rationally designed and successfully synthesized. Moreover, the rate constant of reverse intersystem crossing reaches 2.34 × 104 s-1 as determined by transient spectroscopy. As a result, TADF emission of BNNIO is observed with a photoluminescence quantum yield of 90.72% and a lifetime of 84.76 μs at 415 nm. This universal regulation strategy undoubtedly opens a new avenue for the development of novel purely organic blue light-emitting materials.
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