4.7 Article

Surface Hopping Excited-State Dynamics Study of the Photoisomerization of a Light-Driven Fluorene Molecular Rotary Motor

Journal

JOURNAL OF CHEMICAL THEORY AND COMPUTATION
Volume 7, Issue 7, Pages 2189-2199

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ct200199w

Keywords

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Funding

  1. Volkswagenstiftung
  2. Netherlands Organization for Scientific Research (NWO) [700.57.404]

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We report a theoretical study of the photoisomerization step in the operating cycle of a prototypical fluorene-based molecular rotary motor (1). The potential energy surfaces of the ground electronic state (S-0) and the first singlet excited state (S-1) are explored by semiempirical quantum-chemical calculations using the orthogonalization-corrected OM2 Hamiltonian in combination with a multireference configuration interaction (MRCI) treatment. The OM2/MRCI results for the So and Si minima of the relevant 1-P and 1-M isomers and for the corresponding S-0 transition state are in good agreement with higher-level calculations, both with regard to geometries and energetics. The S-1 surface is characterized at the OM2/MRCI level by locating two S-0-S-1 minimum-energy conical intersections and nearby points on the intersection seam and by computing energy profiles for pathways toward these MECIs. Semiclassical Tully-type trajectory surface hopping (TSH) simulations with on-the-fly OM2/MRCI calculations are carried out to study the excited-state dynamics after photoexcitation to the S-1 state. Fast relaxation to the ground state is observed through the conical intersection regions, predominantly through the lowest-energy one with a strongly twisted central C=C double bond and pyramidalized central carbon atom. The excited-state lifetimes for the direct and inverse photoisomerization reactions (1.40 and 1.79 ps) and the photostationary state ratio (2.7:1) from the TSH-OM2 simulations are in good agreement with the available experimental data (ca. 1.7 ps and 3:1). Excited-state lifetimes, photostationary state ratio, and dynamical details of the TSH-OM2 simulations also agree with classical molecular dynamics simulations using a reparametrized optimized potentials for liquid simulations (OPLS) all-atom force field with ad-hoc surface hops at predefined conical intersection points. The latter approach allows for a more extensive statistical sampling.

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