| Autor: |
Dunning TH Jr; Department of Chemistry, University of Washington, Seattle, Washington 98195, USA., Xu LT; Department of Chemistry, University of Washington, Seattle, Washington 98195, USA. |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of chemical physics [J Chem Phys] 2022 Aug 28; Vol. 157 (8), pp. 084124. |
| DOI: |
10.1063/5.0104693 |
| Abstrakt: |
We extended our studies of the effect of dynamical electron correlation on the covalent bonds in the AH and AF series (A = B-F) to the recoupled pair bonds in the excited a 4 Σ - states of the CH and CF molecules. Dynamical correlation is energetically less important in the a 4 Σ - states than in the corresponding X 2 Π states for both molecules, which is reflected in smaller changes in bond energies (D e ). Changes in the equilibrium bond distance (R e ) and vibrational frequency (ω e ), on the other hand, are influenced by the changes in the slope and curvature of the dynamical electron correlation energy as a function of the internuclear distance R, E DEC (R). In the CH(a 4 Σ - ) state, these changes are much smaller than in the CH(X 2 Π) state, but in the CF(a 4 Σ - ) state, they are larger, reflecting a significant difference in the shapes of E DEC (R) curves. At large R, the shape of E DEC (R) curves for covalent and recoupled pair bonds is similar although different in magnitude. For the CH(a 4 Σ - ) state, E DEC (R) has a minimum at R = R e + 0.72 Å as the orbitals associated with the formation of the recoupled pair bond switch places. E DEC (R) for the CF(a 4 Σ - ) state decreases continuously throughout the bound region of the potential energy curve because the dynamical correlation energy associated with the electrons in the lone pair orbitals is increasing. These results support our earlier conclusion that we still have much to learn about the nature of dynamical electron correlation in molecules. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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