Nature Communications · 2019 · 73 citations · 65 references
Natural SciencesChemistryComputational ChemistryCrystal StructureTheoretical ChemistryChemical BondingCoordination ChemistryLigand BindingMetal-ligand BondingMolecular Orbital TheoryBondingCovalency In Metal-ligand BondsElectronic Structure Of Metal ComplexesIntermolecular Metal-ligand InteractionsLigand Effects On ReactivityLigand Electronic EffectsMetal-ligand CovalencyMolecular Electrostatic Potential
FEUDAL (f's essentially unaffected, d's accommodate ligands) is a longstanding bonding model in actinide chemistry, in which metal-ligand binding uses 6d-orbitals, with the 5f remaining non-bonding. The inverse-trans-influence (ITI) is a case where the model may break down, and it has been suggested that ionic and covalent effects work synergistically in the ITI. Here, we report an experimentally grounded computational study that quantitatively explores the ITI, and in particular the structure-directing role of f-orbital covalency. Strong donor ligands generate a cis-ligand-directing electrostatic potential (ESP) at the metal centre. When f-orbital participation, via overlap-driven covalency, becomes dominant via short actinide-element distances, this ionic ESP effect is overcome, favouring a trans-ligand-directed geometry. This study contradicts the accepted ITI paradigm in that here ionic and covalent effects work against each other, and suggests a clearly non-FEUDAL, structure-directing role for the f-orbitals.
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Generalized Gradient Approximation Made Simple
John P. Perdew, Kieron Burke, Matthias Ernzerhof · Physical Review Letters · 1996 · 211.5K citations · Full text
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Covalency in f-element complexes
Michael L. Neidig, David L. Clark, Richard L. Martin · Coordination Chemistry Reviews · 2012 · 549 citations
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