Nature Communications · 2017 · 170 citations · 58 references
Natural SciencesChemistryCrystal StructureInorganic ChemistrySolid-state ChemistryActinide ChemistryCarbene ComplexesCoordination ChemistryLanthanide ChemistryMetal-ligand BondingTransition Metal ComplexesActinide Oxidation StatesBonding OrbitalsCovalency In Metal-ligand BondsElectronic Structure Of Metal ComplexesLanthanide ReactivityLigand Effects On ReactivityLigand Electronic EffectsOxidation State Equilibria
Across the periodic table the trans-influence operates, whereby tightly bonded ligands selectively lengthen mutually trans metal-ligand bonds. Conversely, in high oxidation state actinide complexes the inverse-trans-influence operates, where normally cis strongly donating ligands instead reside trans and actually reinforce each other. However, because the inverse-trans-influence is restricted to high-valent actinyls and a few uranium(V/VI) complexes, it has had limited scope in an area with few unifying rules. Here we report tetravalent cerium, uranium and thorium bis(carbene) complexes with trans C=M=C cores where experimental and theoretical data suggest the presence of an inverse-trans-influence. Studies of hypothetical praseodymium(IV) and terbium(IV) analogues suggest the inverse-trans-influence may extend to these ions but it also diminishes significantly as the 4f orbitals are populated. This work suggests that the inverse-trans-influence may occur beyond high oxidation state 5f metals and hence could encompass mid-range oxidation state actinides and lanthanides. Thus, the inverse-trans-influence might be a more general f-block principle.
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Isolation and characterization of a uranium(VI)–nitride triple bond
David M. King, Floriana Tuna, Eric J. L. McInnes et al. · Nature Chemistry · 2013 · 290 citations