Chemical Bonding in Isoelectronic NdO2 and SmO22+

Jiaxin Ning, Donald G. Truhlar

Research output: Contribution to journalArticlepeer-review

Abstract

Neodymium dioxide (NdO2) and samarium dioxide cation (SmO22+) are isoelectronic molecules. Here we used calculations of the spin-orbit-free wave functions to study and compare their geometries, spin states, and bonding. We used Kohn-Sham density functional theory with the B97-1 exchange-correlation functional to optimize the geometries and found that the two molecules have different ground spin states and structures. NdO2 favors a linear ONdO triplet structure, and SmO22+ favors a linear SmOO2+ quintet structure. We then used state-averaged complete-active-space self-consistent-field (SA-CASSCF) calculations to investigate the bonding characteristics of NdO2 and SmO22+ in various geometries. We found that in NdOO, one electron is transferred from Nd to O, while in SmO22+, there is no electron transfer between Sm and O. The SA-CASSCF calculation also shows that ONdO has a stronger bonding orbital between a 4f orbital of Nd and a pz orbital of oxygen atoms. We compared three multireference methods, namely, extended multistate complete active space second-order perturbation theory (XMS-CASPT2), extended multistate pair-density functional theory (XMS-PDFT), and compressed multistate pair-density functional theory (CMS-PDFT), for calculating the spin-orbit-free energies of various isomers of both molecules. We found that although XMS-PDFT and CMS-PDFT are at the same cost level as SA-CASSCF, they give results with the same accuracy as given for the much more demanding XMS-CASPT2 calculation. Between the two multistate PDFT methods, CMS-PDFT is better at giving good degeneracies for states that should be degenerate.

Original languageEnglish (US)
Pages (from-to)2295-2305
Number of pages11
JournalJournal of Physical Chemistry A
Volume127
Issue number10
DOIs
StatePublished - Mar 16 2023
Externally publishedYes

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Publisher Copyright:
© 2023 American Chemical Society.

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  • Journal Article

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