Product distributions and rate constants for ion‐molecule reactions in water, hydrogen sulfide, ammonia, and methane

1973 ◽  
Vol 59 (9) ◽  
pp. 4742-4756 ◽  
Author(s):  
W. T. Huntress ◽  
R. F. Pinizzotto
1969 ◽  
Vol 47 (6) ◽  
pp. 957-964 ◽  
Author(s):  
J. A. Herman ◽  
A. G. Harrison

The ion–molecule reactions in vinyl fluoride have been studied as a function of pressure and electron energy. The C2H2+ and C2HF+ fragment ions react predominantly by charge transfer while C2H3+ produces C2H4F+ and C4H5+. The C2H2F+ fragment forms C2H4F+, CHF2+, C2H3F2+, C4H4F+, and probably C2H3+. The rate constants for the individual reactions have been measured. The C2H3F+ ion reacts to form C3H5+, C3H4F+, C3H3F2+, and C4H5F+ (in minor yield), both by a second order and by a third order reaction. The rate constants and product distributions from the individual reactions have been evaluated. A number of consecutive reactions have been identified and shown to be third order processes.


1973 ◽  
Vol 95 (13) ◽  
pp. 4107-4115 ◽  
Author(s):  
Wesley T. Huntress ◽  
Russell F. Pinizzotto ◽  
James B. Laudenslager

1973 ◽  
Vol 4 (35) ◽  
Author(s):  
WESLEY T. JUN. HUNTRESS ◽  
RUSSELL F. JUN. PINIZZOTTO ◽  
JAMES B. LAUDENSLAGER

1991 ◽  
Vol 69 (2) ◽  
pp. 363-367
Author(s):  
Guoying Xu ◽  
Jan A. Herman

Ion/molecule reactions in mixtures of ethyl chloride with C1–C4 alkylamines were studied by ICR mass spectrometry. Ethyl cation transfer to C1–C4 alkylamines proceeds mainly through diethylchloronium ions with rate constants ~3 × 10−10cm3 s−1. In the case of s-butylamine the corresponding rate constant is 0.5 × 10−10 cm3 s−1. Key words: ICR mass spectrometry, ion/molecule reactions, ethylchloride, methylamine, ethylamine, propylamines, butylamines


1976 ◽  
Vol 31 (5) ◽  
pp. 414-421 ◽  
Author(s):  
Karl-Peter Wanczek

Abstract The mass spectrum of tetramethyldiphosphine and the ion chemistries of this compound and of its mixtures with phosphine and dimethylphosphine have been investigated by ion cyclotron resonance spectrometry. Numerous ion molecule reactions have been observed. The rate constants of the two most abundant ions formed by the molecular ion, the tetramethyldiphosphonium ion, H(CH3)2P-P(CH3)2+ and the hexamethyltriphosphonium ion, P3(CH3)6+ , are k2.35≦0.1X10-10 cm3 molecule-1 s-1 and k2.40 = 1.5 X10-10 cm3 molecule -1 s -1 respectively. The structures of several ions have been determined with the aid of their ion-molecule reactions. The ions m/e = 79 and 93 are thought to have the structures HP - P(CH3)H+ and HP-P(CH3)2+ . The most probable structures of the ions m/e = 169 and 183 are HP(CH3)2-P(CH3)-P(CH3)2+ and (CH3)2P-P(CH3) - P(CH3)3+ . The protonated molecule undergoes several ion-molecule reactions, which proceed via an intermediate, m/e = 183, [(CH3)6P3+]* which is detected by double resonance experiments.


1980 ◽  
Vol 87 ◽  
pp. 299-303 ◽  
Author(s):  
M.J. Mcewan ◽  
V. G. Anicich ◽  
W.T. Huntress

Rate constants obtained by the ICR technique are reported for reaction (1), C2H2+ + HCN and reaction (2) HCN+ + C2H2 such that k1 = 3.6 × 10−10 and k2 = 6.9 × 10−10 cm3 molecule−1 s−1, respectively. Differences between these results and other measurements of reaction (1) are discussed. The relevance of reaction (1) to the formation of HC3N in interstellar clouds is also briefly assessed.


RSC Advances ◽  
2020 ◽  
Vol 10 (44) ◽  
pp. 26433-26442
Author(s):  
Yunju Zhang ◽  
Bing He

The reaction between CFCl2CH2O2 radicals and ClO was studied using the B3LYP and CCSD(T) methods associated with the 6-311++G(d,p) and cc-pVTZ basis sets, and subsequently RRKM-TST theory was used to predict the thermal rate constants and product distributions.


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