Electron density analysis of metal-metal bonding in a Ni4 cluster featuring ferromagnetic exchange

Leiszner, Sofie Stampe, Chakarawet, Khetpakorn, Long, Jeffrey R., Nishibori, Eiji, Sugimoto, Kunihisa, Platts, James A. ORCID: https://orcid.org/0000-0002-1008-6595 and Overgaard, Jacob 2023. Electron density analysis of metal-metal bonding in a Ni4 cluster featuring ferromagnetic exchange. Inorganic Chemistry 62 (1) , pp. 192-200. 10.1021/acs.inorgchem.2c03170

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Abstract

We present a combined experimental and theoretical study of the nature of the proposed metal–metal bonding in the tetranuclear cluster Ni4(NPtBu3)4, which features four nickel(I) centers engaged in strong ferromagnetic coupling. High-resolution single-crystal synchrotron X-ray diffraction data collected at 25 K provide an accurate geometrical structure and a multipole model electron density description. Topological analysis of the electron density in the Ni4N4 core using the quantum theory of atoms in molecules clearly identifies the bonding as an eight-membered ring of type [Ni–N−]4 without direct Ni–Ni bonding, and this result is generally corroborated by an analysis of the energy density distribution. In contrast, the calculated bond delocalization index of ∼0.6 between neighboring Ni atoms is larger than what has been found for other bridged metal–metal bonds and implies direct Ni–Ni bonding. Similar support for the presence of direct Ni–Ni bonding is found in the interacting quantum atom approach, an energy decomposition scheme, which suggests the presence of stabilizing Ni–Ni bonding interactions with an exchange-correlation energy contribution approximately 50% of that of the Ni–N interactions. Altogether, while the direct interactions between neighboring Ni centers are too weak and sterically constrained to bear the signature of a topological bond critical point, other continuous measures clearly indicate significant Ni–Ni bonding. These metal–metal bonding interactions likely mediate direct ferromagnetic exchange, giving rise to the high-spin ground state of the molecule.

Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	Advanced Research Computing @ Cardiff (ARCCA) Chemistry
Publisher:	American Chemical Society
ISSN:	0020-1669
Date of First Compliant Deposit:	4 January 2023
Date of Acceptance:	7 December 2022
Last Modified:	11 Jun 2024 16:17
URI:	https://orca.cardiff.ac.uk/id/eprint/155376

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