Catalytic Alkyne and Diyne Metathesis with Mixed Fluoroalkoxy-Siloxy Molybdenum Alkylidyne Complexes
Manuel L. Zier, Sophie Colombel‐Rouen, Henrike Ehrhorn, Dirk Bockfeld, Yann Trolez, Marc Mauduit, Matthias Tamm
Abstract
The reaction of the molybdenum alkylidyne complex [MesC≡Mo{OC(CF3)3}3] (MoF9, Mes = 2,4,6-trimethylphenyl) with the potassium siloxides KOSi(OtBu)3 and KOSi(OtBu)2(OMes) furnished the mixed fluoroalkoxy-siloxy alkylidyne complexes [MesC≡Mo{OC(CF3)3}2{OSi(OtBu)3}] (MoSiF9) and [MesC≡Mo{OC(CF3)3}2{OSi(OtBu)2(OMes)}] (MoSi*F9). A treatment of MoF9, MoSiF9, and MoSi*F9 with an excess of 3-hexyne (EtC≡CEt) afforded labile metallacyclobutadiene (MCBD) complexes with a (C3Et3)Mo core, which are in equilibrium with the corresponding propylidyne (EtC≡Mo) complexes in solution. Thermodynamic parameters for these [2 + 2]-cycloaddition/cycloreversion reactions were determined by van’t Hoff plots, revealing that the nature of the ancillary siloxide ligand exerts a significant effect on the MCBD stability. An X-ray diffraction analysis of MoSi*F9-MCBD provided one of the first accurate crystal structures of a molybdenacyclobutadiene. MoF9, MoSiF9, and MoSi*F9 proved active catalysts for the metathesis of internal alkynes and diynes, with MoSi*F9 showing unprecendented selectivity in the conversion of sterically encumbered 1,3-pentadiynes into symmetrical 1,3,5-triynes and 2-butyne.