التفاصيل البيبلوغرافية
| العنوان: |
The photodissociation dynamics and ultrafast electron diffraction image of cyclobutanone from the surface hopping dynamics simulation. |
| المؤلفون: |
Peng, Jiawei, Liu, Hong, Lan, Zhenggang |
| المصدر: |
Journal of Chemical Physics; 6/14/2024, Vol. 160 Issue 22, p1-13, 13p |
| مصطلحات موضوعية: |
SURFACE dynamics, PERTURBATION theory, MOLECULAR structure, LINEAR accelerators, MOLECULAR evolution, ELECTRON diffraction, VIBRATIONAL spectra |
| مستخلص: |
The comprehension of nonadiabatic dynamics in polyatomic systems relies heavily on the simultaneous advancements in theoretical and experimental domains. The gas-phase ultrafast electron diffraction (UED) technique has attracted significant attention as a unique tool for monitoring photochemical and photophysical processes at the all-atomic level with high temporal and spatial resolutions. In this work, we simulate the UED spectra of cyclobutanone using the trajectory surface hopping method at the extended multi-state complete active space second order perturbation theory (XMS-CASPT2) level and thereby predict the results of the upcoming UED experiments in the Stanford Linear Accelerator Laboratory. The simulated results demonstrate that a few pathways, including the C2 and C3 dissociation channels, as well as the ring opening channel, play important roles in the nonadiabatic reactions of cyclobutanone. We demonstrate that the simulated UED signal can be directly interpreted in terms of atomic motions, which provides a unique way of monitoring the evolution of the molecular structure in real time. Our work not only provides numerical data that help to determine the accuracy of the well-known surface hopping dynamics at the high XMS-CASPT2 electronic-structure level but also facilitates the understanding of the microscopic mechanisms of the photoinduced reactions in cyclobutanone. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
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