Enhanced inverted singlet–triplet gaps in azaphenalenes and non-alternant hydrocarbons
Marc H. Garner, J. Terence Blaskovits, Clémence Corminbœuf
Abstract
Inverted singlet-triplet gaps may lead to novel molecular emitters if a rational design approach can be achieved. We uncover a substituent strategy that enables tuning of the gap and succeed in inducing inversion in near-gapless molecules. Based on known inverted-gap emitters, we design substituted analogs with even more negative singlet-triplet gaps than in the parent systems. The inversion is lost if the reverse substituent-strategy is used. We thus demonstrate a definite set of conceptual design rules for inverted gap molecules.
Topics & Concepts
SubstituentSinglet stateGapless playbackInversion (geology)MoleculeSinglet fissionComputational chemistryDiradicalChemistryBand gapChemical physicsSmall moleculePhotochemistryTriplet stateMaterials scienceStereochemistryPhysicsOptoelectronicsCondensed matter physicsQuantum mechanicsOrganic chemistryExcited stateBiochemistryStructural basinBiologyPaleontologyMolecular Junctions and NanostructuresOrganic Electronics and PhotovoltaicsOrganic Light-Emitting Diodes Research