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Zero-field splitting in nickel(II) complexes: A comparison of DFT and multi-configurational wavefunction calculations
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK).
Stockholm University, Faculty of Science, Department of Physics.
2013 (English)In: Journal of Chemical Physics, ISSN 0021-9606, E-ISSN 1089-7690, Vol. 138, no 6, 064304- p.Article in journal (Refereed) Published
Abstract [en]

The zero-field splitting (ZFS) is an important quantity in the electron spin Hamiltonian for S = 1 or higher. We report calculations of the ZFS in some six- and five-coordinated nickel(II) complexes (S = 1), using different levels of theory within the framework of the ORCA program package [F. Neese, Wiley Interdiscip. Rev.: Comput. Mol. Sci. 2, 73 (2012)]10.1002/wcms.81. We compare the high-end ab initio calculations (complete active space self-consistent field and n-electron valence state perturbation theory), making use of both the second-order perturbation theory and the quasi-degenerate perturbation approach, with density functional theory (DFT) methods using different functionals. The pattern of results obtained at the ab initio levels is quite consistent and in reasonable agreement with experimental data. The DFT methods used to calculate the ZFS give very strongly functional-dependent results and do not seem to function well for our systems.

Place, publisher, year, edition, pages
2013. Vol. 138, no 6, 064304- p.
National Category
Physical Sciences Chemical Sciences
URN: urn:nbn:se:su:diva-87610DOI: 10.1063/1.4790167ISI: 000315054400018OAI: diva2:604872
Available from: 2013-02-12 Created: 2013-02-12 Last updated: 2013-03-26Bibliographically approved

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Kowalewski, JozefOdelius, Michel
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