Bimetallic Mechanism for Alkyne Cyclotrimerization with a Two-Coordinate Fe Precatalyst
Ryan J. Witzke, Diptarka Hait, Khetpakorn Chakarawet, Martin Head‐Gordon, T. Don Tilley
Abstract
The two-coordinate compound (IPr)Fe[N(SiMe3)DIPP] (IPr = 1,3-bis(2,6-diisopropylphenyl)imidazolin-2-ylidene; DIPP = 2,6-diisopropylphenyl) catalyzes the cyclotrimerization of alkynes to arenes. Treatment of the Fe complex with 1 equiv of diphenylacetylene results in the formation of a bimetallic bridging alkyne complex, along with dissociation of IPr from Fe. At elevated temperatures, the bridging alkyne complex undergoes oxidative coupling to form a dimetallacyclopentadiene complex, formally by a one-electron oxidation at each metal center. Each complex catalyzes the cyclotrimerization of diphenylacetylene. Kinetic studies exhibit first-order dependence on the bimetallic complexes, providing further support for the presence of these species in the catalytic cycle. DFT calculations support the experimental mechanistic data and suggest that the catalytic cycle is completed by binding of an alkyne to the diene complex, followed by insertion to form a hexatriene species that then undergoes ring closure to form an inverse sandwich complex, [DIPP(Me3Si)N]Fe(η6-arene)Fe[N(SiMe3)DIPP]. The arene product is then displaced by alkyne to close the catalytic cycle.