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• W4225263963 abstract "The electronic structure of coordination compounds with lanthanide ions is studied by means of density functional theory (DFT) calculations. This work deals with the electronic structure and properties of open-shell systems based on the calculation of multiplet structure and ligand-field interaction, within the framework of the Ligand–Field Density-Functional Theory (LFDFT) method. Using effective Hamiltonian in conjunction with the DFT, we are able to reasonably calculate the low-lying excited states of the molecular [Eu(NO3)3(phenanthroline)2] complex, subjected to the Eu3+ configuration 4f6. The results are compared with available experimental data, revealing relative uncertainties of less than 5% for many energy levels. We also demonstrate the ability of the LFDFT method to simulate absorption spectrum, considering cerocene as an example. Ce M4,5 X-ray absorption spectra are simulated for the complexes [Ce(η8−C8H8)2] and [Ce(η8−C8H8)2][Li(tetrahydrofurane)4], which are approximated by the Ce oxidation states 4+ and 3+, respectively. The results showed a very good agreement with the experimental data for the Ce3+ compound, unlike for the Ce4+ one, where charge transfer electronic structure is still missing in the theoretical model. Therefore this presentation reports the benefits of having a theoretical method that is primarily dedicated to coordination chemistry, but it also outlines limitations and places the ongoing developmental efforts in the broader context of treating complex molecular systems." @default.
• W4225263963 created "2022-05-04" @default.
• W4225263963 creator A5036165179 @default.
• W4225263963 date "2022-05-02" @default.
• W4225263963 modified "2023-10-01" @default.
• W4225263963 title "LFDFT—A Practical Tool for Coordination Chemistry" @default.
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• W4225263963 doi "https://doi.org/10.3390/computation10050070" @default.
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