4.7 Article

Quadratic Spin-Orbit Mechanism of the Electronic g-Tensor

Journal

JOURNAL OF CHEMICAL THEORY AND COMPUTATION
Volume 19, Issue 6, Pages 1765-1776

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jctc.2c01213

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Understanding the relationship between the electronic g-tensor and the electronic structure is crucial for interpreting electron paramagnetic resonance spectra correctly. In this study, we investigated the quadratic spin-orbit (SO) contributions to the g-shift in heavy transition metal complexes. We found that the dominant quadratic SO term, spin-Zeeman (SO2/SZ), generally leads to a negative contribution to the g-shift. Moreover, we analyzed how the SO2/SZ contribution affects the individual principal components of the g-tensor in combination with the linear orbital-Zeeman (SO/OZ) contribution.
Understanding how the electronic g-tensor is linked to the electronic structure is desirable for the correct interpretation of electron paramagnetic resonance spectra. For heavy-element compounds with large spin-orbit (SO) effects, this is sti l l not completely clear. We report our investigation of quadratic SO contributions to the g-shi f t in heavy transition metal complexes. We implemented third-order perturbation theory in order to analyze the contributions arising from frontier molecular spin orbitals (MSOs). We show that the dominant quadratic SO term-spin-Zeeman (SO2/SZ)-generally makes a negative contribution to the g-shift, irrespective of the particular electronic configuration or molecular symmetry. We further analyze how the SO2/SZ contribution adds to or subtracts from the linear orbital-Zeeman (SO/OZ) contribution to the individual principal components of the g-tensor. Our study suggests that the SO2/SZ mechanism decreases the anisotropy of the g-tensor in early transition metal complexes and increases it in late transition metal complexes. Finally, we apply MSO analysis to the investigation of g-tensor trends in a set of closely related Ir and Rh pincer complexes and evaluate the influence of different chemical factors (the nuclear charge of the central atom and the terminal ligand) on the magnitudes of the g-shifts. We expect our conclusions to aid the understanding of spectra in magnetic resonance investigations of heavy transition metal compounds.

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