Unraveling the coordination isomerism by ligand hyperfine NMR shifts
| Authors | |
|---|---|
| Year of publication | 2026 |
| Type | Article in Periodical |
| Magazine / Source | Chemical Science |
| MU Faculty or unit | |
| Citation | |
| web | DOI: 10.1039/D5SC09905F |
| Doi | https://doi.org/10.1039/D5SC09905F |
| Keywords | NMR spectroscopy; hyperfine shift; DFT calculations; spin density; Ru(III) complex; metal coordination |
| Attached files | |
| Description | The hyperfine (Curie) NMR shifts of ligand atoms in the open-shell coordination compound report subtle details of the spin distribution around the central metal atom. In this work, we propose hyperfine NMR shifts as simple and extremely sensitive indicators of the ligand coordination geometry. This is demonstrated for equatorial versus axial isomers of neutral octahedral [Ru(acac)Cl2L2] compounds, and rationalized by two distinct mechanisms of transmission of the spin density unraveled using density-functional theory analysis. The positional interchange of the two chlorides and the two pnictogen-based ligands (L) induces modifications in the singly occupied molecular orbital composition and the related Fermi-contact hyperfine interactions of the probed atoms of the acac ligand, resulting in distinct 1H and 13C NMR spectral fingerprints. The demonstrated symmetry-driven spin-transmission mechanisms have general validity, which offers hyperfine NMR shift as a tool to probe the geometry of various classes of coordination compounds, including transition-metal catalysts and metalloenzymes. |
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