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• W1997908740 endingPage "9487" @default.
• W1997908740 startingPage "9479" @default.
• W1997908740 abstract "The coupled-cluster method with a large basis set with quasi-relativistic effective core potentials on the halogens was utilized to investigate the ground electronic state X 1Σ+ of the IHBr anion. A semi-global, three-dimensional potential energy surface was obtained via spline interpolation of ab initio data. Variational rovibrational calculations were carried out with this potential energy surface, and assignment of fundamentals and low-lying overtones, as well as combination bands, is presented for IH(D)Br anions. Photodetachment spectra for IH(D)Br−+hν→[IH(D)Br]+e− were computed using three-dimensional time-independent real and complex L2 methods and a recently developed real L2 wave packet propagation technique; all methods employed a previous London–Eyring–Polanyi–Sato empirical potential for the neutral system. Well resolved fine structure is found in photodetachment spectra of IHBr−. This structure is assigned to bending excitation based on analysis of the wave functions and the neutral potential energy surface near the Franck–Condon region. This fine structure is largely eliminated in the IDBr− spectrum. The photodetachment spectrum for the first excited asymmetric stretch of IHBr− shows a new feature that is associated with sampling of the transition state region of the neutral surface. Spin-orbit corrected multi-reference configuration interaction calculations indicate that the first excited electronic state is only about 0.06 eV above the ground electronic state of the neutral IHBr system in the Franck–Condon region. The model empirical potential used in the calculations of photodetachment spectra is shown to have roughly the average behavior of these two ab initio potentials." @default.
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• W1997908740 date "2000-12-01" @default.
• W1997908740 modified "2023-09-26" @default.
• W1997908740 title "Theoretical study of the photodetachment spectroscopy of the IHBr and IDBr anions" @default.
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• W1997908740 doi "https://doi.org/10.1063/1.1319877" @default.
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