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A Very Short Uranium(IV)-Rhodium(I) Bond with Net Double-Dative Bonding Character
Erli Lu1, Ashley J Wooles1, Matthew Gregson1
1School of Chemistry, The University of Manchester, Oxford Road, Manchester, M13 9PL, UK.
Abstract:
Reaction of [U{C(SiMe3 )(PPh2 )}(BIPM)(μ-Cl)Li(TMEDA)(μ-TMEDA)0.5 ]2 (BIPM=C(PPh2 NSiMe3 )2 ; TMEDA=Me2 NCH2 CH2 NMe2 ) with [Rh(μ-Cl)(COD)]2 (COD=cyclooctadiene) affords the heterotrimetallic UIV -RhI2 complex [U(Cl)2 {C(PPh2 NSiMe3 )(PPh[C6 H4 ]NSiMe3 )}{Rh(COD)}{Rh(CH(SiMe3 )(PPh2 )}]. This complex has a very short uranium-rhodium distance, the shortest uranium-rhodium bond on record and the shortest actinide-transition metal bond in terms of formal shortness ratio. Quantum-chemical calculations reveal a remarkable RhI→→ UIV net double dative bond interaction, involving RhI 4dz2 - and 4dxy/xz -type donation into vacant UIV 5f orbitals, resulting in a Wiberg/Nalewajski-Mrozek U-Rh bond order of 1.30/1.44, respectively. Despite being, formally, purely dative, the uranium-rhodium bonding interaction is the most substantial actinide-metal multiple bond yet prepared under conventional experimental conditions, as confirmed by structural, magnetic, and computational analyses.
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When atoms gain or lose electrons to achieve a more stable electron configuration they form ions. Ionic bonds are electrostatic attractions between ions with opposite charges. Ionic compounds are rigid and brittle when solid and may dissociate into their constituent ions in water. Covalent compounds, by contrast, remain intact unless a chemical reaction breaks them.
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