التفاصيل البيبلوغرافية
| العنوان: |
Photoionization of aziridine: Nonadiabatic dynamics of the first six low-lying electronic states of the aziridine radical cation. |
| المؤلفون: |
Rani, Vadala Jhansi, Kanakati, Arun Kumar, Mahapatra, S. |
| المصدر: |
Journal of Chemical Physics; 9/7/2024, Vol. 161 Issue 9, p1-19, 19p |
| مصطلحات موضوعية: |
AB initio quantum chemistry methods, ATOMIC structure, ELECTRONIC density of states, TIME-dependent Schrodinger equations, PHOTOELECTRON spectra |
| مستخلص: |
In this article, the theoretical photoionization spectroscopy of the aziridine (C2H5N) molecule is investigated. To start with, we have optimized the geometry of this molecule at the neutral electronic ground state at the density functional theory/augmented correlation-consistent polarized valence triple zeta level of theory using the G09 program. The electronic structure calculations were restricted to the first six low-lying electronic states in order to account for the experimental photoelectron spectrum of the C2H5N molecule. The first six low-lying electronic states ( X ̃ 2 A ′ , A ̃ 2 A ′ , B ̃ 2 A ″ , C ̃ 2 A ″ , D ̃ 2 A ′ , and E ̃ 2 A ′ ) of the potential energy surfaces (PESs) are calculated by both equation of motion-ionization potential-coupled cluster singles and doubles and multi-configuration quasi-degenerate perturbation theory ab initio quantum chemistry methods along the dimensionless normal displacement coordinates in which multiple conical intersections were established among the considered electronic states. A (6 × 6) model vibronic Hamiltonian is constructed on a diabatic electronic basis, using the symmetry selection rules and Taylor series expansion. The Cs symmetry point group of the aziridine molecule leads to electronic states symmetry of either A′ or A″, and these states are close in energy, due to which the same symmetry electronic states avoid each other. To get a smooth diabatic PES, a fourfold diabatization scheme is used, which is implemented in the General Atomic and Molecular Electronic Structure Systems suite of programs. All the parameters used in the diabatic vibronic coupling model Hamiltonian are calculated in terms of the normal modes of vibrational coordinates. Finally, the vibronic model Hamiltonian constructed for the coupled six electronic states is used to solve both time-independent and time-dependent Schrödinger equations using the multi-configuration time-dependent Hartree program module to obtain the dynamical observables. The theoretical vibronic band structure is found to be in good accord with the available experimental results. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
Complementary Index |
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