Bond-forming and electron-transfer reactivity between Ar2+ and N2. Issue 19 (6th May 2021)
- Record Type:
- Journal Article
- Title:
- Bond-forming and electron-transfer reactivity between Ar2+ and N2. Issue 19 (6th May 2021)
- Main Title:
- Bond-forming and electron-transfer reactivity between Ar2+ and N2
- Authors:
- Armenta Butt, Sam
Price, Stephen D. - Abstract:
- Abstract : Electron transfer between Ar 2+ and N2 involves both complexation and direct dynamics; a stripping-style pathway generates ArN + . Abstract : Collisions between Ar 2+ 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 Ar 2+ and N2 reactants. Here Ar + is generated in its ground ( 2 P) state and N2 + is primarily in the low vibrational levels of the C 2 Σu + 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 Ar 2+ ( 1 D and 1 S) populating N2 + * in its dissociative C 2 Σu +, 2 2 Πg and D 2 Πg states. Formation of ArN + + N + proceeds via a direct mechanism. The ArN + is formed, with significant vibrational excitation, in its ground (XAbstract : Electron transfer between Ar 2+ and N2 involves both complexation and direct dynamics; a stripping-style pathway generates ArN + . Abstract : Collisions between Ar 2+ 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 Ar 2+ and N2 reactants. Here Ar + is generated in its ground ( 2 P) state and N2 + is primarily in the low vibrational levels of the C 2 Σu + 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 Ar 2+ ( 1 D and 1 S) populating N2 + * in its dissociative C 2 Σu +, 2 2 Πg and D 2 Πg states. Formation of ArN + + N + proceeds via a direct mechanism. The ArN + is formed, with significant vibrational excitation, in its ground (X 3 Σ − ) state. Formation of N + + N + is also observed as a consequence of double electron transfer forming N2 2+ . The exoergicity of the subsequent N2 2+ dissociation reveals the population of the A 1 Πu and D 3 Πg dication states. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 23:Issue 19(2021)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 23:Issue 19(2021)
- Issue Display:
- Volume 23, Issue 19 (2021)
- Year:
- 2021
- Volume:
- 23
- Issue:
- 19
- Issue Sort Value:
- 2021-0023-0019-0000
- Page Start:
- 11287
- Page End:
- 11299
- Publication Date:
- 2021-05-06
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d1cp00918d ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 16858.xml