Abstract
The inversion of the lowest singlet and triplet excited states, observed in several triangle-shaped organic molecules containing conjugated carbon and nitrogen atoms, is an astonishing result that implies the breakdown of Hund's rule. The phenomenon attracted interest for its potential towards triplet harvesting in organic LEDs. On a more fundamental vein, the singlet-triplet (ST) inversion sheds new light on the role of electron correlations in the excited state landscape of pi-conjugated molecules. Relying on the celebrated Pariser-Parr-Pople model, the simplest model for correlated electrons in pi-conjugated systems, we demonstrate that the ST inversion does not require triangle-shaped molecules nor any specific molecular symmetry. Indeed, the ST inversion does not require strictly non-overlapping HOMO and LUMO orbitals, but rather a small gap and a small exchange integral between the frontier orbitals.
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Supplementary Information
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Supplementary Information to "Shining light on inverted singlet-triplet emitters"
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Easy-to-use (PPP-based) computational tool for the calculation of HOMO-LUMO exchange integral
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An easy-to-use (Pariser-Parr-Pople - based) computational tool is made publicly available for the calculation of HOMO-LUMO exchange integral.
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