Related Experiment Video
Updated: Jun 27, 2026

Photoelectron Imaging of Anions Illustrated by 310 Nm Detachment of F−
Published on: July 27, 2018
Experimental and theoretical study of the ion-ion mutual neutralization reactions Ar(+)+SF(n)- (n=6, 5, and 4)
Joseph C Bopp1, Thomas M Miller, Albert A Viggiano
1Space Vehicles Directorate, Air Force Research Laboratory, Hanscom Air Force Base, Massachusetts 01731-3010, USA.
Abstract:
The ion-ion mutual neutralization reactions Ar(+)+SF(n) (-)-->Ar+SF(n) (n=6, 5, and 4) have been studied in a flowing afterglow-Langmuir probe (FALP) apparatus at 300 K and 1 Torr of He buffer gas. Electron concentrations and product ion fractions were measured, and neutralization rate constants of 4.0 x 10(-8), 3.8 x 10(-8), and 4 x 10(-8) cm(3) s(-1) for SF(6) (-), SF(5) (-), and SF(4) (-), respectively, were derived, with uncertainties of +/-25% (+/-35% for SF(4) (-)). During the neutralization process, excited neutrals are generated that are able to dissociate to neutral fragments. In the case of SF(6), the formation of SF(5) and SF(4), and similarly in the case of SF(5), the formation of SF(4) and SF(3) were observed and quantified. The mechanism of primary and secondary reaction was analyzed in detail, and rate constants for the dissociative electron attachments e(-)+SF(5)-->F(-)+SF(4) (k=3 x 10(-9) cm(3) s(-1),+/-40%) and e(-)+SF(3)-->F(-)+SF(2) (k=2 x 10(-8) cm(3) s(-1),+400%,-75%) were also derived. The experimental ion-ion neutralization rate constants were found to be in good agreement with estimates from an optimum two-state double-passage Landau-Zener model. It was also found that energy partitioning in the neutralization is related to the extent of electronic excitation of Ar generated by the electron transfer processes.
Related Concept Videos
Acids, Bases and Neutralization Reactions
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by water loss...
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism
Diazonium Group Substitution: –OH and –H
Nucleophilic Aromatic Substitution: Addition–Elimination (SNAr)
The reaction begins with an attack of the nucleophile on the carbon that holds the leaving group. This results in the delocalization of the π electrons over the ring carbons. The resonance interaction between the...
Ion Exchange

