First Principle Prediction of Intramolecular Singlet Fission and Triplet Triplet Annihilation Rates

Intramolecular singlet fission and triplet–triplet annihilation (TTA) has been experimentally observed and reported. However, problems remain in theoretically accounting for the corresponding intramolecular electronic couplings and their rates. We used the fragment excitation difference (FED) scheme to calculate the coupling with states from restricted active-space spin-flip configuration interaction. We investigated three covalently linked pentacene dimers via a phenyl group in an ortho-, meta-, and para-arrangement. The singlet fission and TTA couplings were enhanced when two chromophores were covalently linked. With the Fermi golden rule, both the estimated singlet fission and TTA rates were in line with the experimental results. For systems with significant singlet-fission coupling, charge-transfer components were observed in the excited states involved, and charge-transfer states were also seen within 1 eV above the singlet excited states. Our approach allows for an analysis of through-bond versus through-space singlet fission in the full electronic wave functions. The FED scheme is useful for calculating intramolecular singlet-fission and TTA couplings.