The electronic emission spectrum of triatomic hydrogen. II. The perpendicular bands near 7100 Å

1980 ◽  
Vol 58 (8) ◽  
pp. 1250-1258 ◽  
Author(s):  
G. Herzberg ◽  
J. K. G. Watson

The strongest emission bands of H3 and D3 near 7100 Å are shown to be [Formula: see text] bands even though of a somewhat unusual structure. Because of the large width of the lines (the same as those of the 5600 Å [Formula: see text] bands) the only method of analysis is by model bands whose parameters are changed until the best fit between observed and calculated spectrum is obtained. As expected on the basics of the line width the lower state is found to be identical with that of the 5600 Å band, i.e., 2s2A1′, while the upper state is 3p2E′. The band structure of a [Formula: see text] band depends strongly on the value of ζ, the electronic angular momentum. When as in the present case ζ is close to 1, pseudo-branches with a constant N – K form the most characteristic features of the [Formula: see text] band. The ζ value determined here for the 3p2E′ state of D3 is 0.8775 which is very close to the ab initio value of King and Morokuma after the latter has been corrected for quenching by the zero-point vibration as a result of Jahn–Teller interaction. In addition the band structure shows clearly the effects of Λ-type doubling and Λ-type resonance which is made especially large by Jahn–Teller distortion. The final B0 value of D3 in the 3p2E′ state, i.e., B0 = 21.16 cm−1, is smaller than the predicted value (21.61 cm−1) for the ground state of D3+ suggesting that the 3pe′ orbital is anti-bonding in agreement with the predictions of King and Morokuma.

2007 ◽  
Vol 40 (12) ◽  
pp. 3807-3810 ◽  
Author(s):  
S Thomas Lee ◽  
K Raveendranath ◽  
Rajive M Tomy ◽  
Nibu A George ◽  
S Jayalekshmi ◽  
...  

2020 ◽  
Author(s):  
Marta L. Vidal ◽  
Michael Epshtein ◽  
Valeriu Scutelnic ◽  
Zheyue Yang ◽  
Tian Xue ◽  
...  

We report a theoretical investigation and elucidation of the x-ray absorption spectra of neutral benzene and of the benzene cation. The generation of the cation by multiphoton ultraviolet (UV) ionization as well as the measurement of<br>the carbon K-edge spectra of both species using a table-top high-harmonic generation (HHG) source are described in the companion experimental paper [M. Epshtein et al., J. Phys.<br>Chem. A., submitted. Available on ChemRxiv]. We show that the 1sC -> pi transition serves as a sensitive signature of the transient cation formation, as it occurs outside of the spectral window of the parent neutral species. Moreover, the presence<br>of the unpaired (spectator) electron in the pi-subshell of the cation and the high symmetry of the system result in significant differences relative to neutral benzene in the spectral features associated with the 1sC ->pi* transitions. High-level calculations using equation-of-motion coupled-cluster theory provide the interpretation of the experimental spectra and insight into the electronic structure of benzene and its cation.<br>The prominent split structure of the 1sC -> pi* band of the cation is attributed to the interplay between the coupling of the core -> pi* excitation with the unpaired electron<br>in the pi-subshell and the Jahn-Teller distortion. The calculations attribute most of<br>the splitting (~1-1.2 eV) to the spin coupling, which is visible already at the Franck-Condon structure, and estimate the additional splitting due to structural relaxation to<br>be around ~0.1-0.2 eV. These results suggest that x-ray absorption with increased resolution might be able to disentangle electronic and structural aspects of the Jahn-Teller<br>effect in benzene cation.<br>


1995 ◽  
Vol 60 (9) ◽  
pp. 1429-1434
Author(s):  
Martin Breza

Using semiempirical CNDO-UHF method the adiabatic potential surface of 2[Cu(OH)6]4- complexes is investigated. The values of vibration and vibronic constants for Eg - (a1g + eg) vibronic interaction attain extremal values for the optimal O-H distance. The Jahn-Teller distortion decreases with increasing O-H distance. The discrepancy between experimentally observed elongated bipyramid of [Cu(OH)6]4- in Ba2[Cu(OH)6] and the compressed one obtained by quantum-chemical calculation is explainable by hydrogen bonding of the axial hydroxyl group.


2021 ◽  
Vol 490 ◽  
pp. 229519
Author(s):  
Renier Arabolla Rodríguez ◽  
Nelcy Della Santina Mohallem ◽  
Manuel Avila Santos ◽  
Demetrio A. Sena Costa ◽  
Luciano Andrey Montoro ◽  
...  

1989 ◽  
Vol 03 (04) ◽  
pp. 355-359 ◽  
Author(s):  
S.L. YUAN ◽  
B.H. HOU ◽  
S.Z. JIN ◽  
W. WANG ◽  
G.G. ZHENG ◽  
...  

The preliminary study on the electron spin resonance (ESR) for the Bi-Sr-Ca-Cu-O system with different superconducting transition temperatures has been made at room temperature. It is found that the Lande factor g-values are increased with increasing zero resistance temperature T c0 but width between peaks ΔH pp of the ESR spectrum decreased with increasing T c0 . These might be attributed to the spin-orbit coupling of the magnetic ions and the Jahn-Teller distortion in the perpendicular component.


2005 ◽  
Vol 117 (41) ◽  
pp. 6904-6908 ◽  
Author(s):  
Ian J. Blackmore ◽  
Adam J. Bridgeman ◽  
Neil Harris ◽  
Mark A. Holdaway ◽  
John F. Rooms ◽  
...  

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