ABSOLUTE INTEGRAL CROSS SECTIONS FOR THE STATE-SELECTED ION–MOLECULE REACTION ${{{\rm{N}}}_{2}}^{+}({X}^{2}{{{\rm{\Sigma }}}_{{\rm{g}}}}^{+}$;v+= 0–2) + C2H2IN THE COLLISION ENERGY RANGE OF 0.03–10.00 eV

2016 ◽  
Vol 827 (1) ◽  
pp. 17 ◽  
Author(s):  
Yuntao Xu ◽  
Bo Xiong ◽  
Yih Chung Chang ◽  
C. Y. Ng
2017 ◽  
Vol 19 (15) ◽  
pp. 9778-9789 ◽  
Author(s):  
Yuntao Xu ◽  
Bo Xiong ◽  
Yih-Chung Chang ◽  
Yi Pan ◽  
Po Kam Lo ◽  
...  

We report detailed integral cross sections and ab initio quantum calculations for the state-selected ion–molecule reaction .


2017 ◽  
Vol 19 (28) ◽  
pp. 18619-18627 ◽  
Author(s):  
Bo Xiong ◽  
Yih-Chung Chang ◽  
Cheuk-Yiu Ng

The integral cross sections for the H2+(v+ = 1–3; N+ = 0–3) + Ne → NeH+ + H reaction have been measured in the collision energy range of 0.05–2.00 eV for comparison of recent quantum dynamic predictions.


1968 ◽  
Vol 23 (12) ◽  
pp. 2080-2083 ◽  
Author(s):  
D. Hyatt ◽  
K. Lacmann

A Bendix time of flight mass spectrometer has been modified to enable the determination of some ion-molecule reaction cross sections in the energy range 1 — 100 eV.In the reactions studiedX+ + D2 → XD++Dwhere X may be Ar, N2 or CO, the results obtained agree with the predictions of the polarization theory in the range below 10 eV despite the fact that no intermediate complex is formed at these energies. Between about 10—50 eV where spectator stripping occurs the cross section follows an approximate E-l dependence. Above these energies the results are consistent with a transition to a region in which knock-on processes predominate and where an impulse approximation treatment would be valid.


2016 ◽  
Vol 18 (32) ◽  
pp. 22509-22515 ◽  
Author(s):  
Hongwei Song ◽  
Anyang Li ◽  
Hua Guo ◽  
Yuntao Xu ◽  
Bo Xiong ◽  
...  

A combined experimental–theoretical study of the rovibrationally state-selected ion–molecule reactions H2O+(X2B1; v1+v2+v3+; NKa+Kc++) + H2 (D2) → H3O+ (H2DO+) + H (D), where (v1+v2+v3+) = (000), (020), and (100) and NKa+Kc++ = 000, 111, and 211.


2017 ◽  
Vol 19 (13) ◽  
pp. 8694-8705 ◽  
Author(s):  
Yuntao Xu ◽  
Bo Xiong ◽  
Yih Chung Chang ◽  
C. Y. Ng

The quantum-rotational- and vibrational-state effects on the chemical reactivity of H2O+ ion toward HD have been examined in detail in a wide kinetic energy range of 0.03–10.00 eV.


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