A Spirocyclic Parabanic Acid Masked N-Heterocyclic Carbene as Thermally Latent Pre-Catalyst for Polyamide 6 Synthesis and Epoxide Curing.

1,3-Dicyclcohexyl-6,9-dimethyl-1,3,6,9-tetraazaspiro[4.4]non-7-ene-2,4-dione, a spirocyclic parabanic acid derivative of N,N-dimethylimidazole, is used as thermally latent, protected N-heterocyclic carbene (NHC) in polymerizing anhydride-cured epoxide resins, and azepan-2-one, respectively. The protected carbene is synthesized from 1,3-dimethylimidazolium-2-carboxylate in the presence of two equivalents of cyclohexyl isocyanate.

Reversible N-Heterocyclic Carbene-Induced α-H Abstraction in Tungsten(VI) Imido Dialkyl Dialkoxide Complexes.

The first reversible N-heterocyclic carbene (NHC) induced α-H abstraction in tungsten(VI) imido-dialkyl dialkoxide complexes is reported. Treatment of W(NAr)(CH Ph) (OtBu) (Ar=2,6-dichlorophenyl, 2,6-dimethylphenyl, 2,6-diisopropylphenyl) with different NHCs leads to the formation of complexes of the type W(NAr)(CHPh)(NHC)(CH Ph)(OtBu) in excellent isolated yields of up to 96 %. The highly unusual release of the tert-butoxide ligand as tBuOH in the course of the reaction was observed.

Latent and Air-Stable Pre-Catalysts for the Polymerization of Dicyclopentadiene: From Penta- to Hexacoordination in Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes.

The pentacoordinated, 16-valence electron (VE) Mo imido alkylidene N-heterocyclic carbene (NHC) complexes I1-I5 and the hexacoordinated 18-VE Mo imido alkylidene NHC complexes 1-4, 8, 10 and 12 containing a chelating ligand have been prepared and used as thermally latent catalysts in the ring-opening metathesis polymerization (ROMP) of dicyclopentadiene (DCPD). Both 10 and 12 are the first Mo imido alkylidene complexes with a chelating alkylidene featuring a carboxylate group. Complexes I1-I3 and I5 as well as 1-4 proved to be fully thermally latent in the presence of DCPD.

Grubbs-Hoveyda type catalysts bearing a dicationic N-heterocyclic carbene for biphasic olefin metathesis reactions in ionic liquids.

The novel dicationic metathesis catalyst [(RuCl2(H2ITapMe2)(=CH-2-(2-PrO)-C6H4))(2+) (OTf(-))2] (Ru-2, H2ITapMe2 = 1,3-bis(2',6'-dimethyl-4'-trimethylammoniumphenyl)-4,5-dihydroimidazol-2-ylidene, OTf(-) = CF3SO3 (-)) based on a dicationic N-heterocyclic carbene (NHC) ligand was prepared. The reactivity was tested in ring opening metathesis polymerization (ROMP) under biphasic conditions using a nonpolar organic solvent (toluene) and the ionic liquid (IL) 1-butyl-2,3-dimethylimidazolium tetrafluoroborate [BDMIM(+)][BF4 (-)]. The structure of Ru-2 was confirmed by single crystal X-ray analysis.