Abstract
The discovery of triangular-shaped organic molecules bearing an inverted singlet-triplet (INVEST) energy gap opened the way for a new strategy to increase the internal quantum efficiency of organic light-emitting diodes by enhancing the Reverse Intersystem Crossing (RISC) process thanks to a downhill process. However, all the molecular systems showing a negative ΔEST suffer from both a vanishing Spin-Orbit Coupling between the lowest singlet (S1) and triplet (T1) excited states and high energy differences with higher-lying singlet and triplet excited states, precluding their involvement in the spin conversion process.
In this work we proposed a new design strategy entailing the extension of the triangulene cores by connecting two INVEST triangulene units to form Uthrene- and Zethrene-like systems, doped with N and B atoms. A detailed inspection of the resulting molecular orbital distribution allowed rationalizing the electronic structure properties obtained employing wavefunction-based methods (NEVPT2, EOM-CCSD, SCS-CC2), showing how the Uthrene-like architecture can give origin to the energy proximity between the lowest singlet and triplet excited states, in some cases leading to their energy inversion. By feeding a kinetic model with the non-radiative rate constants calculated from first principle we showed how the Extended INVEST (X−INVEST) design strategy can open new pathways to boost the spin conversion process and the population of the emissive S1 excited state.
Supplementary materials
Title
Supplementary materials
Description
Molecular orbitals of the different compounds, composition of the excited states, percentage of double excitations in the CASSCF wavefunction, CC2 and SCS-CC2 excited energies of 2N-U and 2N-Z, CASSCF excited states energies of 2N-U and 2N-Z for the (8,8), (10,10) and (12,12) active spaces, description of the kinetic model
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