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New Insights into the State Trapping of UV-Excited Thymine.

ABSTRACT: After UV excitation, gas phase thymine returns to a ground state in 5 to 7 ps, showing multiple time constants. There is no consensus on the assignment of these processes, with a dispute between models claiming that thymine is trapped either in the first (S?) or in the second (S?) excited states. In the present study, a nonadiabatic dynamics simulation of thymine is performed on the basis of ADC(2) surfaces, to understand the role of dynamic electron correlation on the deactivation pathways. The results show that trapping in S? is strongly reduced in comparison to previous simulations considering only non-dynamic electron correlation on CASSCF surfaces. The reason for the difference is traced back to the energetic cost for formation of a CO ? bond in S?.

SUBMITTER: Stojanovic L

PROVIDER: S-EPMC6273395 | biostudies-literature | 2016 Nov

REPOSITORIES: biostudies-literature

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New Insights into the State Trapping of UV-Excited Thymine.

Stojanović Ljiljana L Bai Shuming S Nagesh Jayashree J Izmaylov Artur F AF Crespo-Otero Rachel R Lischka Hans H Barbatti Mario M

Molecules (Basel, Switzerland) 20161123 11

After UV excitation, gas phase thymine returns to a ground state in 5 to 7 ps, showing multiple time constants. There is no consensus on the assignment of these processes, with a dispute between models claiming that thymine is trapped either in the first (S₁) or in the second (S₂) excited states. In the present study, a nonadiabatic dynamics simulation of thymine is performed on the basis of ADC(2) surfaces, to understand the role of dynamic electron correlation on the deactivation pathways. The ...[more]

PMID: 27886099

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