Electron correlation in the Iron(II) Porphyrin by NOF approximations
Juan Felipe Huan Lew-Yee, Jorge M. del Campo, Mario Piris

TL;DR
This study evaluates electron correlation effects in Iron(II) porphyrin's spin states using advanced natural orbital functionals, revealing the importance of dynamic correlation in accurately predicting the ground state.
Contribution
It introduces the use of GNOF, a new functional that correlates all electrons and orbitals, improving the prediction of the stable spin state of FeP.
Findings
GNOF predicts the triplet as the ground state after dynamic correlation correction.
Previous PNOF methods favored the quintet as the ground state.
Dynamic correlation significantly influences the stability order of FeP's spin states.
Abstract
The relative stability of the singlet, triplet, and quintet spin states of Iron(II) porphyrin (FeP) represents a challenging problem for electronic structure methods. While it is currently accepted that the ground state is a triplet, multiconfigurational wavefunction-based methods predict a quintet, and density functional approximations vary between triplet and quintet states, leading to a prediction that highly depends on the features of the method employed. The recently proposed Global Natural Orbital Functional (GNOF) aims to provide a balanced treatment between static and dynamic correlation, and together with the previous Piris Natural Orbital Functionals (PNOFs), allowed us to explore the importance of each type of correlation in the stability order of the states of FeP with a method that conserves the spin of the system. It is noteworthy that GNOF correlates all electrons in all…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsMolecular Junctions and Nanostructures · Surface Chemistry and Catalysis · Magnetism in coordination complexes
