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On the existence of collective interactions reinforcing the metal-ligand bond in organometallic compounds

Jordi Poater, Pascal Vermeeren, Trevor A. Hamlin, F. Matthias Bickelhaupt, Miquel Solà

2023Nature Communications13 citationsDOIOpen Access PDF

Abstract

Recently, Sowlati-Hashjin et al. 1 concluded that the nature of the Li–C chemical bond in LiCF 3 differs significantly from that in LiCPh 3 (Ph = phenyl). Whereas the Li–C bond of LiCF 3 is classified as a conventional two-center two-electron bond (exchange-correlation interaction collectivity index, ICI XC = 0.910, ICI XC > 0.9 and close to 1), that of LiCPh 3 is categorized as a collective bond (ICI XC = 0.393). The authors claim that collective bonds take place in systems composed of MAR 3 (M = metal; A = C, B or Al; R = substituent) when M forms a stronger bond with the substituents R than with the central atom A. They claim the M–A interaction is either destabilizing or weakly stabilizing, whilst the 1,3-M•••R interactions are strongly stabilizing, but their method does not provide a causal mechanism that would demonstrate the correctness of this interpretation of the ICI XC index. Here, we prove the opposite, namely, that the Li–CPh 3 bond is not reinforced or provided by collective interactions, but that it is weakened by 1,3-M•••R contacts, which reduce the bond overlap. On top of that, there is 1,3-M•••R closed-shell overlap that further reduces the stability through Pauli repulsion. Taken together, our results suggest that there is no need to define the collective interaction as a new type of chemical bond.

Topics & Concepts

Ligand (biochemistry)BondGroup 2 organometallic chemistryMetalChemistryMoleculeReceptorOrganic chemistryBusinessBiochemistryFinanceChemical Thermodynamics and Molecular StructureHistory and advancements in chemistryInorganic and Organometallic Chemistry
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