Bimolecular reactions of S2+ with Ar, H2 and N2: reactivity and dynamics.

The reactivity, energetics and dynamics of bimolecular reactions between S2+ and three neutral species (Ar, H2 and N2) have been studied using a position-sensitive coincidence methodology at centre-of-mass collision energies below 6 eV. This is the first study of bimolecular reactions involving S2+, a species detected in planetary ionospheres, the interstellar medium, and in anthropogenic manufacturing processes. The reactant dication beam employed consists predominantly of S2+ in the ground 3P state, but some excited states are also present. Most of the observed reactions involve the ground state of S2+, but the dissociative electron transfer reactions appear to exclusively involve excited states of this atomic dication. We observe exclusively single electron-transfer between S2+ and Ar, a process which exhibits strong forward scatting typical of the Landau-Zener style dynamics observed for other dicationic electron transfer reactions. Following collisions between S2+ + H2, non-dissociative and dissociative single electron-transfer reactions were detected. The dynamics here show evidence for the formation of a long-lived collision complex, [SH2]2+, in the dissociative single electron-transfer channel. The formation of SH+ was not observed. In contrast, the collisions of S2+ + N2 result in the formation of SN+ + N+ in addition to the products of single electron-transfer reactions.

Bimolecular reactions of CH2CN2+ with Ar, N2 and CO: reactivity and dynamics.

The reactivity, energetics and dynamics of bimolecular reactions between CH2CN2+ and three neutral species (Ar, N2 and CO) have been studied using a position sensitive coincidence methodology at centre-of-mass collision energies of 4.3-5.0 eV. This is the first study of bimolecular reactions involving CH2CN2+, a species relevant to the ionospheres of planets and satellites, including Titan. All of the collision systems investigated display two collision-induced dissociation (CID) channels, resulting in the formation of C+ + CH2N+ and H+ + HC2N+. Evidence for channels involving further dissociation of the CID product HC2N+, forming H + CCN+, were detected in the N2 and CO systems. Proton-transfer from the dication to the neutral species occurs in all three of the systems via a direct mechanism. Additionally, there are product channels resulting from single electron transfer following collisions of CH2CN2+ with both N2 and CO, but interestingly no electron transfer following collisions with Ar. Electronic structure calculations of the lowest energy electronic states of CH2CN2+ reveal six local geometric minima: both doublet and quartet spin states for cyclic, linear (CH2CN), and linear isocyanide (CH2NC) molecular geometries. The lowest energy electronic state was determined to be the doublet state of the cyclic dication. The ready generation of C+ ions by collision-induced dissociation suggests that the cyclic or linear isocyanide dication geometries are present in the [CH2CN]2+ beam.

Bond-forming and electron-transfer reactivity between Ar2+ and N2.

Collisions between Ar2+ and N2 have been studied using a coincidence technique at a centre-of-mass (CM) collision energy of 5.1 eV. Four reaction channels generating pairs of monocations are observed: Ar+ + N2+, Ar+ + N+, ArN+ + N+ and N+ + N+. The formation of Ar+ + N2+ is the most intense channel, displaying forward scattering but with a marked tail to higher scattering angles. This scattering, and other dynamics data, is indicative of direct electron transfer competing with a 'sticky' collision between the Ar2+ and N2 reactants. Here Ar+ is generated in its ground (2P) state and N2+ is primarily in the low vibrational levels of the C2Σu+ state. A minor channel involving the initial population of higher energy N2+ states, lying above the dissociation asymptote to N+ + N, which fluoresce to stable states of N2+ is also identified. The formation of Ar+ + N+ by dissociative single electron transfer again reveals the involvement of two different pathways for the initial electron transfer (direct or complexation). This reaction pathway predominantly involves excited states of Ar2+ (1D and 1S) populating N2+* in its dissociative C2Σu+, 22Πg and D2Πg states. Formation of ArN+ + N+ proceeds via a direct mechanism. The ArN+ is formed, with significant vibrational excitation, in its ground (X3Σ-) state. Formation of N+ + N+ is also observed as a consequence of double electron transfer forming N22+. The exoergicity of the subsequent N22+ dissociation reveals the population of the A1Πu and D3Πg dication states.

Bond-forming and electron-transfer reactivity between Ar2+ and O2.

The reactivity, energetics and dynamics of the bimolecular reactions between Ar2+ and O2 have been studied using a position sensitive coincidence methodology at a collision energy of 4.4 eV. Four bimolecular reaction channels generating pairs of product ions are observed, forming: Ar+ + O2+, Ar+ + O+, ArO+ + O+ and O+ + O+. The formation of Ar+ + O2+ is a minor channel, involving forward scattering, and generates O2+ in its ground electronic state. This single electron transfer process is expected to be facile by Landau-Zener arguments, but the intensity of this channel is low because the electron transfer pathways involve multi-electron processes. The formation of Ar+ + O+ + O, is the most intense channel following interactions of Ar2+ with O2, in agreement with previous experiments. Many different combinations of Ar2+ and product electronic states contribute to the product flux in this channel. Major dissociation pathways of the nascent O2+* ion involve the ion's first and second dissociation limits. Unusually, the experimental results clearly show the involvement of a short-lived collision complex [ArO2]2+ in this channel. The formation of O+ and ArO+ involves direct abstraction of O- from O2 by Ar2+. There is scant evidence of the involvement of a collision complex in this bond forming pathway. The ArO+ product appears to be formed in the first excited electronic state (2Π). The formation of O+ + O+ results from dissociative double electron transfer via an O22+ intermediate. The exoergicity of the dissociation of the nascent O22+ intermediate is in good agreement with previous work investigating the unimolecular dissociation of this dication.