Gas-phase synthesis of [O＝U–X]+ (X = Cl, Br and I) from a UO22+ precursor using ion-molecule reactions and an [O＝U≡CH]+ intermediate.

Difficulty in the preparation of gas-phase ions that include U in middle oxidation states(III , IV) have hampered efforts to investigate intrinsic structure, bonding and reactivity of model species. Our group has used preparative tandem mass spectrometry (PTMS) to synthesize a gas-phase U-methylidyne species, [O＝U≡CH]+, by elimination of CO from [UO2(C≡CH)]+ [M. J. van Stipdonk, I. J. Tatosian, A. C. Iacovino, A. R. Bubas, L. Metzler, M. C. Sherman and A. Somogyi, J. Am. Soc. Mass Spectrom., 2019, 30, 796–805], which has been used as an intermediate to create products such as [OUN]+ and [OUS]+ by ion-molecule reactions. Here, we investigated the reactions of [O＝U≡CH]+ with a range of alkyl halides to determine whether the methylidyne is a also a useful intermediate for production and study of the oxy-halide ions [OUX]+, where X = Cl, Br and I, formally U(IV) species for which intrinsic reactivity data is relatively scarce. Our experiments demonstrate that [OUX]+ is the dominant product ion generated by reaction [O＝U≡CH]+ with neutral regents such as CH3Cl, CH3CH2Br and CH2＝CHCH2I. [ABSTRACT FROM AUTHOR]