Abstract

Manganese(I) complexes [(Cp(CH2)nNHCMes)Mn(CO)2] (2a, n = 1; 2b, n = 2) bearing Cp tethered NHC ligands have been prepared in good yield from [CpMn(CO)3] and N-mesitylimidazole as main components, using a novel synthetic strategy based on the anchoring of an imidazolium moiety to the coordinated Cp ligand, followed by an intramolecular photochemical CO substitution for the pendent NHC moiety generated in situ upon addition of a base. The catalytic performances of 2a–b in the hydrosilylation of 2-acetonaphthone with Ph2SiH2 were found to be essentially indifferent to the length of the linker between the Cp and the NHC moieties, and lower than the one of the nontethered [Cp(CO)2Mn(IMes)] (1) parent complex. Still, the presence of Cp tethered NHC ligands allowed isolation and full characterization of monocarbonyl η2-silane complexes [(Cp(CH2)nNHCMes)Mn(CO)(η2-H–SiHPh2)] (8a, n = 1; 8b, n = 2), which are generated upon photochemical reactions of 2a–b with diphenylsilane. Both of these silane complexes are ina...

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