Abstract
Simple molybdenum methyl, carbene, and carbyne complexes, [CH3--MoF], [CH2=MoHF], and [CH[triple chemical bond]MoH(2)F], were formed by the reaction of laser-ablated molybdenum atoms with methyl fluoride and isolated in an argon matrix. These molecules provide a persistent photoreversible system through alpha-hydrogen migration between the carbon and metal atoms: The methyl and carbene complexes are produced by applying UV irradiation (240-380 nm) while the carbyne complex is depleted, and the process reverses on irradiation with visible light (lambda>420 nm). An absorption at 589.3 cm(-1) is attributed to the Mo--F stretching mode of [CH3--MoF], which is in fact the most stable of the plausible products. Density functional theory calculations show that one of the alpha-hydrogen atoms of the carbene complex is considerably bent toward the metal atom (angle-spherical HCMo=84.5 degrees ), which provides evidence of a strong agostic interaction in the triplet ground state. The calculated C[triple chemical bond]Mo bond length in the carbyne is in the range of triple-bond values in methylidyne complexes.
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