Peridinin Torsional Distortion and Bond-Length Alternation Introduce Intramolecular Charge-Transfer and Correlated Triplet Pair Intermediate Excited States.

Abstract

The nature of intramolecular charge transfer (ICT) and the mechanism of intramolecular singlet fission (SF) in peridinin remain open research questions. Obtaining an understanding of the population evolution from the bright state to dark state following a photoinduced electronic transition is critical. Unambiguously describing this evolution in peridinin, and light-harvesting carotenoids in general, has proven elusive experimentally and computationally. To offer a balanced description of the bright- and dark-state electronic structures, we here apply ab initio multireference perturbation theory quantum chemistry-the density matrix renormalization group self-consistent field and complete-active-space self-consistent field with second-order N-electron valence perturbation theory. At traditional bright- (S2) and dark-state (S1) optimized geometries, we find that an additional correlated triplet pair state and ICT state are derived from the canonical polyene Bu (S3) and 3Ag (S4) dark singlet excited states, respectively. Whereas the S3 state's physical properties are insensitive to peridinin's allene-tail donor and lactone ring acceptor functionalization, the S4 state exhibits a markedly enhanced oscillator strength and highest occupied molecular orbital-lowest unoccupied molecular orbital transition density. These changes suggest that the ICT character stems from mixing between the bright S2 and putatively dark S4.