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A “non-magnetic” triplet bismuthinidene enabled by relativity

MPS-Authors
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Pang,  Yue
Research Group Cornellà, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Nöthling,  Nils
Service Department Lehmann (EMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Leutzsch,  Markus
Service Department Farès (NMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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van Gastel,  Maurice
Research Group van Gastel, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Goddard,  Richard
Service Department Lehmann (EMR), Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Wagner,  Lucas
Research Group Cornellà, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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SantaLucia,  Daniel
Research Department Neese, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Neese,  Frank
Research Department Neese, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Cornella,  Josep
Research Group Cornellà, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Citation

Pang, Y., Nöthling, N., Leutzsch, M., Kang, L., Bill, E., van Gastel, M., et al. (2022). A “non-magnetic” triplet bismuthinidene enabled by relativity. ChemRxiv: the Preprint Server for Chemistry. doi:10.26434/chemrxiv-2022-d3jl7.


Cite as: https://hdl.handle.net/21.11116/0000-000C-2649-8
Abstract
Isolation and stabilization of main group diradical species have posed a synthetic challenge over the years due to their intrinsic high reactivity. Herein we report on a large-scale synthesis and isolation of a mono-coordinate bismuthinidene featuring a rigid and bulky ligand, which protects the Bi(I) center. The compound was characterized by its unique spectroscopic features (UV-vis and NMR), but more prominently, by its magnetic properties. Multiconfigurational quantum chemical calculations predict the ground state of the compound to be dominated by a spin-triplet. Further support for this electronic structure description was obtained through correlation of theory to experimental XRD, XAS, and UV-Vis data. However, all magnetic measurements (EPR, NMR and SQUID) point to a diamagnetic compound. This apparent discrepancy can be explained by an extremely large spin-orbit coupling (SOC) that leads to an unprecedented zero-field splitting of more than 8000 cm‒1, thus leaving a MS = 0 magnetic sublevel thermally isolated in the electronic ground state. The extremely large SOC effect is a result of the low-coordination number of the bismuth center in interplay with its heavy element nature.