Abstract
It is customary when computing ro−vibrational transitions in molecules to invoke the Born−Oppenheimer separation between nuclear and electronic motion. However, it is known from accurate calculations on H2+ and H2 that the first-order (diagonal adiabatic) and second-order (nonadiabatic) corrections are not negligible and are both important. In the present work, we have made an ab initio implementation of the Bunker and Moss formalism for the nonadiabatic correction and applied it to H2 and H2O. From comparison to accurate calculations for H2, we find that we can obtain good results for the nonadiabatic correction using CI singles to treat the electronically excited states if we scale the results, but we must go beyond the SCF approximation to obtain an accurate diagonal adiabatic correction. For H2O, we find that the first-order correction is more important than the second-order correction for bending energy levels, but the second-order correction is more important than the first-order correction for stre...
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.