A Multi‐Functional New Acceptor for Ultra‐Broad Multiple Emission, Long‐Persistence Thermally Activated Delayed Fluorescence and Room Temperature Phosphorescence

Abstract Aiming to design new efficient organic triplet emitters, here a new electron‐accepting moiety 11,13‐dihydro‐12H‐dibenzo[a,c]imidazo[4,5‐i]phenazin‐12‐one ( BIPO ) are reported. Three new BIPO derivatives containing long alkyl chains, namely DBIPO (acceptor only), DBIPOBr (acceptor containing bromine atoms), and DBIPOAc with acridan moieties in a donor‐acceptor‐donor configuration, are designed and investigated. Efficient room temperature phosphorescence (RTP) is detected for the three compounds, stemming from a high‐lying (anti‐Kasha type) triplet emission occurring in the acceptor moiety. Additionally, the tetrahydrofuran‐ and dichloromethane DBIPOAc solutions show (i) a dual‐band photoluminescence profile stemming from anti‐Kasha emissions from high‐lying charge‐transfer ( 1 CT) and locally excited ( 1 LE) states, and (ii) a thermally activated delayed fluorescence (TADF) from the same high‐lying 1 CT state. Importantly, DBIPOAc doped in rigid nonpolar polymer Zeonex simultaneously exhibits both TADF and RTP, with the emission quantum yield reaching 69.6%. Due to these properties, the BIPO derivatives constitute promising candidates as multi‐functional new emitters for the preparation of active layers of electroluminescent devices and optical oxygen/pressure sensors. The reasons for these interesting properties are discussed in detail.