Designing Rh(I)-Half-Sandwich Catalysts for Alkyne [2+2+2] Cycloadditions

Metal-mediated [2+2+2] cycloadditions of unsaturated molecules to cyclic and polycyclic organic compounds are a versatile synthetic route affording good yields and selectivity under mild conditions. In the last two decades,in silicoinvestigations have unveiled important details about the mechanism and the energetics of the whole catalytic cycle. Particularly, a number of computational studies address the topic of half-sandwich catalysts which, due to their structural fluxionality, have been widely employed, since the 1980s. In these organometallic species, the metal is coordinated to an aromatic ring, typically the ubiquitous cyclopentadienyl anion, C5H5-(Cp) or to the Cp moiety of a larger polycyclic aromatic ligand (Cp '). During the catalytic process, the metal continuously 'slips' on the ring, changing its hapticity. This phenomenon of metal slippage and its implications for the catalyst's performance are discussed in this work, referring to the most important computational mechanistic studies reported in literature for Rh(I) half-metallocenes, with the purpose of providing hints for a rational design of this class of compounds.

Automated summary

Metal-mediated [2+2+2] cycloadditions are a versatile synthetic route, and computational studies have revealed important mechanistic details. Half-sandwich catalysts feature structural fluxionality, with the metal continuously 'slipping' on the ring during catalysis, impacting catalyst performance.