Spectroscopic Identification of the Carbyne Hydride Structure of the Dehydrogenation Product of Methane Activation by Osmium Cations.

The present work explores the structures of species formed by dehydrogenation of methane (CH) and perdeuterated methane (CD) by the 5d transition metal cation osmium (Os). Using infrared multiple photon dissociation (IRMPD) action spectroscopy and density functional theory (DFT), the structures of the [Os,C,2H] and [Os,C,2D] products are explored. This study complements previous work on the related species formed by dehydrogenation of methane by four other 5d transition metal cations (M = Ta, W, Ir, and Pt). Osmium cations are formed in a laser ablation source, react with methane pulsed into a reaction channel downstream, and the resulting products spectroscopically characterized through photofragmentation using the Free-Electron Laser for IntraCavity Experiments (FELICE) in the 300-1800 cm range. Photofragmentation was monitored by the loss of H/D. Comparison of the experimental spectra and DFT calculated spectra leads to identification of the ground state carbyne hydride, HOsCH (A') as the species formed, as previously postulated theoretically. Further, a full description of the systematic spectroscopic shifts observed for deuterium labeling of these complexes, some of the smallest systems to be studied using IRMPD action spectroscopy, is achieved. A full rotational contour analysis explains the observed linewidths as well as the observation of doublet structures in several bands, consistent with previous observations for HIrCH (A'). Graphical Abstract ᅟ.