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Updated: May 16, 2026

Imine Metathesis by Silica-Supported Catalysts Using the Methodology of Surface Organometallic Chemistry
Published on: October 18, 2019
N-heterocyclic silylene complexes of group VI transition metal carbonyls
Eduard Glok1, Moritz Schanbacher1, Christian Luz1
1Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg, Germany. u.radius@uni-wuerzburg.de.
Abstract:
The reactivity and coordination behavior of several N-heterocyclic silylenes R2NHSi (R = tBu, Mes, Dipp) with respect to group 6 transition metal acetonitrile carbonyl complexes fac-[M(CO)3(MeCN)3] (M = Cr, Mo) are reported. The first examples of threefold NHSi substituted chromium(0) and molybdenum(0) carbonyl complexes, mer-[Cr(CO)3(tBu2NHSi)3] (1), mer-[Mo(CO)3(tBu2NHSi)3] (2), and mer-[Mo(CO)3(Mes2NHSi)3] (3), were isolated from the reactions of fac-[M(CO)3(CH3CN)3] (M = Cr, Mo) with three equivalents of tBu2NHSi or Mes2NHSi. The NHSi ligands adopt meridional arrangements in these octahedral complexes in solution and in the solid state, which contrasts with the related NHC complexes that adopt facial geometries. The reaction of fac-[Cr(CO)3(MeCN)3] with Mes2NHSi led to the substitution of only two acetonitrile ligands to yield mer-[Cr(CO)3(Mes2NHSi)2(MeCN)] 4, as did the reaction of fac-[Mo(CO)3(MeCN)3] with Dipp2NHSi to give mer-[Mo(CO)3(Dipp2NHSi)2(MeCN)] 5. Thus, the steric bulk of the silylenes Mes2NHSi (for Cr) and Dipp2NHSi (for Mo) can be regarded as steric limits for a threefold substitution. The remaining acetonitrile ligand of 4 is prone to further substitution, as was demonstrated with the reaction of 4 with pyridine (= py), dimethylamino-pyridine (= DMAP), tert-butyl isocyanide (= CN-tBu), and 1,3,4,5-tetramethyl-imidazolin-2-ylidene (= IMeMe), which led to the formation of the complexes mer-[Cr(CO)3(Mes2NHSi)2(py)] 6, mer-[Cr(CO)3(Mes2NHSi)2(DMAP)] 7, mer-[Cr(CO)3(Mes2NHSi)2(CN-tBu)] 8, and mer-[Cr(CO)3(Mes2NHSi)2(IMeMe)] 9. In these complexes, the NHSi ligands are located in trans positions.
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