Intrinsic reactivity of [OUCH]+ : Apparent synthesis of [OUS]+ by reaction with CS2.

RATIONALE: Building on our report that collision-induced dissociation (CID) can be used to create the highly reactive U-alkylidyne species [O=U≡CH]+ , our goal was to determine whether the species could be as an intermediate for synthesis of [OUS]+ by reaction with carbon disulfide (CS2 ). METHODS: Cationic uranyl-propiolate precursor ions were generated by electrospray ionization, and multiple-stage CID in a linear trap instrument was used to prepare [O=U≡CH]+ . Neutral CS2 was admitted into the trap through a modified He inlet and precision leak valves. RESULTS: The [O=U≡CH]+ ion reacts with CS2 to generate [OUS]+ . CID of [OUS]+ causes elimination of the axial sulfide ligand to generate [OU]+ . Using isotopically labeled reagent, we found that [OUS]+ reacts with O2 to create [UO2 ]+ . CONCLUSIONS: [O=U≡CH]+ proves to be a useful reagent ion for synthesis of [OUS]+ , a species that to date has only been created by gas-phase reactions of U+ and U2+ . Dissociation of [OUS]+ to create [OU]+ , but not [US]+ , and the efficient conversion of the species into [UO2 ]+ , is consistent with the relative differences in U-O and U-S bond energies.

Intrinsic chemistry of [OUCH]+: reactions with H2O, CH3C[triple bond, length as m-dash]N and O2.

We report the first experimental study of the intrinsic chemistry of a U-methylidyne species, focusing on reaction of [OUCH]+ with H2O, O2 and CH3C[triple bond, length as m-dash]N in the gas phase. DFT was also used to determine reaction pathways, and establish the mechanism by which [OUCH]+ is formed through collision-induced dissociation of [UO2(C[triple bond, length as m-dash]CH)]+.