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Lookup NU author(s): Ataollah Amini,
Emeritus Professor Anthony Harriman
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This investigation explores the use of contemporary quantum chemistry to mimic the light-induced, intramolecular charge-transfer processes that occur in 2-methyl-2,3-dihydrobenz[d,e]isoquinoline (DHBIQ) in polar solvents. Thus, the computed excited-state manifold, comprising two locally excited π,π* singlets, a locally excited ππ* triplet, and a charge-transfer (CT) state, is in excellent agreement with the experimental findings. It is shown that, whereas the energies of the various locally excited states are insensitive to molecular geometry and environment, the energy of the CT state depends markedly on structure and solvent polarity. The most favorable charge-transfer interactions occur within a distorted geometry that is midway between the axial and equatorial conformers identified for the ground state. The calculated nuclear and solvent reorganization energies are in good agreement with prior experimental work. Molecular dynamics simulations were employed to estimate the change in Gibbs free energy accompanying charge transfer and this latter value, used in conjunction with the reorganization energy, allows reproduction of the experimental activation energy. Finally, the electronic coupling matrix element for charge transfer was computed by identifying the intersection point for potential energy surfaces associated with the CT state and the lowest-energy π,π* excited singlet state. The derived value (TDA = 206 cm-1) is close to the experimental result (TDA = 140 cm-1) obtained by application of classical Marcus theory. Overall, it is concluded that quantum chemical methods allow meaningful calculation of the parameters controlling the rate of charge transfer in this system.
Author(s): Amini A, Harriman A
Publication type: Article
Publication status: Published
Journal: Journal of Physical Chemistry A
ISSN (print): 1089-5639
ISSN (electronic): 1520-5215
Publisher: American Chemical Society
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