Theoretical studies have predicted the presence of a forbidden 1B state in proximity to the strongly allowed 1B excited state in polyenes and carotenoids. The 1B state is invariably predicted to have a very low oscillator strength, which precludes direct optical spectroscopic assignment. We report here a direct UV-vis optical spectroscopic feature assigned to the 1B state of S-2-peridinin, a synthetic analogue of the naturally occurring carotenoid, peridinin. The shift of the ground state dipole of S-2-peridinin compared to natural peridinin enhances the oscillator strength of absorption from the ground state to the 1B state by 2 orders of magnitude relative to peridinin. It is postulated that this is due to a quadrupolar electrostatic field generated from the more central location of the lactone ring along the polyene chain in S-2-peridinin. MNDO-PSDCI and EOM-CCSD calculations provide a theoretical basis for this assignment and explain the unique properties of the 1B state and why the transition from the ground state to this state has such a low oscillator strength in most other polyenes and carotenoids.
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http://dx.doi.org/10.1021/acs.jpca.7b10001 | DOI Listing |
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