An extended E ⊗ e Jahn-Teller Hamiltonian for large-amplitude motion: Application to vibrational conical intersections in CH3SH and CH3OH

被引:4
|
作者
Dawadi, Mahesh B. [1 ]
Thapaliya, Bishnu P. [1 ,2 ]
Perry, David S. [1 ]
机构
[1] Univ Akron, Dept Chem, Akron, OH 44325 USA
[2] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
来源
JOURNAL OF CHEMICAL PHYSICS | 2017年 / 147卷 / 04期
关键词
H STRETCHING VIBRATIONS; INTERNAL-ROTATION; AB-INITIO; FORCE-FIELD; METHANOL; QUANTUM; STATES; ADIABATICITY; COORDINATE; PATHWAYS;
D O I
10.1063/1.4994699
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
An extended E circle times e Jahn-Teller Hamiltonian is presented for the case where the (slow) nuclear motion extends far from the symmetry point and may be described approximately as motion on a sphere. Rather than the traditional power series expansion in the displacement from the C-3v symmetry point, an expansion in the spherical harmonics is employed. Application is made to the vibrational Jahn-Teller effect in CH3XH, with X = S, O, where the equilibrium CXH angles are 83 degrees and 72 degrees, respectively. In addition to the symmetry-required conical intersection (CI) at the C-3v symmetry point, ab initio calculations reveal sets of six symmetry-allowed vibrational CIs in each molecule. The CIs for each molecule are arranged differently in the large-amplitude space, and that difference is reflected in the infrared spectra. The CIs in CH3SH are found in both eclipsed and staggered geometries, whereas those for CH3OH are found only in the eclipsed geometry near the torsional saddle point. This difference between the two molecules is reflected in the respective high-resolution spectra in the CH stretch fundamental region. Published by AIP Publishing.
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页数:9
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