Delayed fluorescence from molecules with an inverted singlet-triplet gap is studied computationally, and the effect of gold(I) metalation and coordination on optical properties is investigated. The results suggest that this new family of complexes may be the first organometallic DFIST emitters reported.
Delayed fluorescence from molecules with an inverted singlet-triplet gap (DFIST) is the consequence of the unusual reverse order of the lowest excited singlet (S-1) and triplet (T-1) states of thermally activated delayed fluorescence (TADF) emitters. Heptazine (1,3,4,6,7,9,9b-heptaazaphenalene) derivatives have an inverted singlet-triplet gap thanks to the combination of multiple resonance (MR) effects and a significant double excitation character. Here, we study computationally the effect of gold(I) metalation and coordination on the optical properties of heptazine (molecule 4) and the phosphine-functionalized 2,5,8-tris(dimethylphosphino)heptazine derivatives (molecules 1-3). Ab initio calculations at the approximate second-order coupled cluster (CC2) and extended multiconfigurational quasi degenerate perturbation theory at the second order (XMC-QDPT2) levels show that molecules 1-4 have an inverted singlet- triplet gap due to the alternating spatial localization of the electron and hole of the exciton in the heptazine core. A non-vanishing one-electron spin-orbit coupling operator matrix element between T-1 and S-1((S-1|H-SO|T-1)) and a fast S-1? T(1 )intersystem crossing rate constant (k(ISC)) calculated at the XMC-QDPT2(12,12) level of theory for molecule 4 suggest that this new family of complexes may be the first organometallic DFIST emitters reported.
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