A quantum-mechanical study of chemical reaction and charge-transfer processes in the (Ar + H2)+ system
Author:
Publisher
Elsevier BV
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Reference29 articles.
1. State selected ion–molecule reactions by a TESICO technique. II. Separation of the reactant spin–orbit states in the reaction Ar+(2P3/2, 2P1/2)+H2(D2)→ArH+(ArD+)+H(D)
2. State selected ion–molecule reactions by a TESICO technique. III. H2+(v)+Ar→ArH++H, Ar++H2: Observation of enhanced charge‐transfer cross sections at near resonance
3. Zum Stoßmechanismus bimolekularer Reaktionen Teil II: Der Abstreifmechanismus der Reaktionen Ar++ H2(D2) → ArH++ H (ArD++ D) bei Energien > 20 eV
4. Charge‐Exchange Cross Sections for Argon Ions in H2 and D2 below 1 keV
5. Translational energy dependence of Ar++XY→ArX++Y (XY=H2,D2,HD) from thermal to 30 eV c.m.
Cited by 24 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Quantum-Mechanical Treatment for Charge-Transfer Processes in Ion-Molecule Collisions;Advances in Chemical Physics;2007-03-14
2. State-Selected and State-to-State Ion-Molecular Reaction Dynamics by Photoionization and Differential Reactivity Methods;Advances in Chemical Physics;2007-03-14
3. State Selected Charge Transfer and Chemical Reactions by the Tesico Technique;Advances in Chemical Physics;2007-03-14
4. Theoretical study of collision-induced dissociation in state-selected collisions of H2+(v)+Ar and HD+(v)+Ar;Chemical Physics;2003-09
5. Theoretical study of the reactions of Ar++HX(v=0) and Ar+HX+(v) (X=H and D) at E=0.1 eV using the trajectory surface hopping method;The Journal of Chemical Physics;2002-02-15
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