Oxygen cation
- Formula: O2+
- Molecular weight: 31.9983
- IUPAC Standard InChIKey: KMHJKRGRIJONSV-UHFFFAOYSA-N
- CAS Registry Number: 12185-07-8
- Chemical structure:
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Ion clustering data
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Michael M. Meot-Ner (Mautner) and Sharon G. Lias
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. Searches may be limited to ion clustering reactions. A general reaction search form is also available.
Clustering reactions
By formula: O2+ + CO2 = (O2+ • CO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 41. ± 4. | kJ/mol | AVG | N/A | Average of 4 out of 6 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 73.2 | J/mol*K | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
ΔrS° | 79.1 | J/mol*K | DT | Illies, 1988 | gas phase; ΔrH(0 K)=41.0 kJ/mol |
ΔrS° | 86.6 | J/mol*K | N/A | Dotan, Davidson, et al., 1978 | gas phase; switching reaction(O2+)O2, Entropy change calculated or estimated; Conway and Janik, 1970 |
ΔrS° | 84. | J/mol*K | N/A | Meot-Ner (Mautner) and Field, 1977 | gas phase; Entropy change calculated or estimated, DG>, ΔrH> |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 18. | kJ/mol | DT | Rakshit and Warneck, 1981 | gas phase |
ΔrG° | 18. | kJ/mol | FA | Dotan, Davidson, et al., 1978 | gas phase; switching reaction(O2+)O2, Entropy change calculated or estimated; Conway and Janik, 1970 |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
39. | 600. | PHPMS | Meot-Ner (Mautner) and Field, 1977 | gas phase; Entropy change calculated or estimated, DG>, ΔrH> |
By formula: (O2+ • CO2) + CO2 = (O2+ • 2CO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 36. ± 2. | kJ/mol | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
ΔrH° | 31. | kJ/mol | PHPMS | Meot-Ner (Mautner) and Field, 1977 | gas phase; Entropy change is questionable |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.2 | J/mol*K | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
ΔrS° | 63. | J/mol*K | PHPMS | Meot-Ner (Mautner) and Field, 1977 | gas phase; Entropy change is questionable |
By formula: (O2+ • 2CO2) + CO2 = (O2+ • 3CO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 26. ± 1. | kJ/mol | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 82.8 | J/mol*K | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
By formula: (O2+ • 3CO2) + CO2 = (O2+ • 4CO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 21. ± 1. | kJ/mol | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 82.0 | J/mol*K | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
By formula: (O2+ • 4CO2) + CO2 = (O2+ • 5CO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 19. ± 2. | kJ/mol | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 83.7 | J/mol*K | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase |
By formula: (O2+ • 5CO2) + CO2 = (O2+ • 6CO2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 17. | kJ/mol | PHPMS | Hiraoka, Nakajima, et al., 1988 | gas phase; Entropy change calculated or estimated |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84. | J/mol*K | N/A | Hiraoka, Nakajima, et al., 1988 | gas phase; Entropy change calculated or estimated |
By formula: O2+ + H2O = (O2+ • H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 67. | kJ/mol | FA | Adams and Bohme, 1970 | gas phase; switching reaction(O2+)SO2, ΔrH> |
By formula: O2+ + Kr = (O2+ • Kr)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 32. | kJ/mol | PDiss | Jarrold, Misev, et al., 1984 | gas phase |
By formula: O2+ + N2O = (O2+ • N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 56.1 | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
ΔrH° | 45. ± 2. | kJ/mol | DT | Illies, 1988 | gas phase; ΔrH(0 K)=45.2 kJ/mol |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 96. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
ΔrS° | 64.0 | J/mol*K | DT | Illies, 1988 | gas phase; ΔrH(0 K)=45.2 kJ/mol |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
37. | 200. | FA | Adams and Bohme, 1970 | gas phase; switching reaction(O2+)O2 |
By formula: (O2+ • N2O) + N2O = (O2+ • 2N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 31. | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
By formula: (O2+ • 2N2O) + N2O = (O2+ • 3N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 25. | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 79. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
By formula: (O2+ • 3N2O) + N2O = (O2+ • 4N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 22. | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
By formula: (O2+ • 4N2O) + N2O = (O2+ • 5N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 20. | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 96. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
By formula: (O2+ • 5N2O) + N2O = (O2+ • 6N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 18. | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
By formula: (O2+ • 6N2O) + N2O = (O2+ • 7N2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 16. | kJ/mol | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84. | J/mol*K | PHPMS | Hiraoka, Fujimaki, et al., 1994 | gas phase |
By formula: O2+ + N2 = (O2+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 21. ± 1. | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
ΔrH° | 22. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase |
ΔrH° | 24. | kJ/mol | PHPMS | Janik and Conway, 1967 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 72.8 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
ΔrS° | 66.1 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase |
ΔrS° | 79.1 | J/mol*K | PHPMS | Janik and Conway, 1967 | gas phase |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
0.0 | 296. | FA | Howard, Bierbaum, et al., 1972 | gas phase |
By formula: (O2+ • N2) + N2 = (O2+ • 2N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 19. ± 1. | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
ΔrH° | 18. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 79.9 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
ΔrS° | 57.7 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable |
By formula: (O2+ • 2N2) + N2 = (O2+ • 3N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 18. ± 1. | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
ΔrH° | 15. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 82.0 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
ΔrS° | 50.6 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable |
By formula: (O2+ • 3N2) + N2 = (O2+ • 4N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 17. ± 1. | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 94.1 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
3. | 204. | HPMS | Speller and Fitaire, 1983 | gas phase |
By formula: (O2+ • 4N2) + N2 = (O2+ • 5N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.3 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67.8 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
3. | 184. | HPMS | Speller and Fitaire, 1983 | gas phase |
By formula: (O2+ • 5N2) + N2 = (O2+ • 6N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.3 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67.4 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
By formula: (O2+ • 6N2) + N2 = (O2+ • 7N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9.5 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 77.4 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
By formula: (O2+ • 7N2) + N2 = (O2+ • 8N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8.8 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 80.8 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
By formula: (O2+ • 8N2) + N2 = (O2+ • 9N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.9 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 79.9 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
By formula: (O2+ • 9N2) + N2 = (O2+ • 10N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 87.0 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
By formula: (O2+ • 10N2) + N2 = (O2+ • 11N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6. ± 1. | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84.5 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase |
By formula: (O2+ • N2 • O2) + N2 = (O2+ • 2N2 • O2)
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
2. | 230. | HPMS | Speller and Fitaire, 1983 | gas phase |
By formula: O2+ + O2S = (O2+ • O2S)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrG° | 40. | kJ/mol | FA | Adams and Bohme, 1970 | gas phase; switching reaction(O2+)O2; Conway and Janik, 1970 |
By formula: O2+ + O2 = (O2+ • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 41. ± 5. | kJ/mol | AVG | N/A | Average of 5 out of 6 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.7 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
ΔrS° | 104.7 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase |
ΔrS° | 84. | J/mol*K | PHPMS | Durden, Kebarle, et al., 1969 | gas phase |
ΔrS° | 86.2 | J/mol*K | PHPMS | Yang and Conway, 1964 | gas phase |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
16. | 300. | DT | Rakshit and Warneck, 1981 | gas phase |
14. | 300. | DT | Rakshit and Warneck, 1980 | gas phase |
14. | 296. | FA | Howard, Bierbaum, et al., 1972 | gas phase |
25. | 200. | FA | Adams and Bohme, 1970 | gas phase |
By formula: (O2+ • O2) + N2 = (O2+ • N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 42.3 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable |
By formula: (O2+ • O2) + O2 = (O2+ • 2O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 25. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase |
ΔrH° | 28.7 ± 0.3 | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 110. | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
ΔrS° | 133.0 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase |
By formula: (O2+ • 2O2) + O2 = (O2+ • 3O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.4 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase |
ΔrH° | 10.6 ± 0.4 | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.2 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
ΔrS° | 82.8 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase |
By formula: (O2+ • 3O2) + O2 = (O2+ • 4O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase |
ΔrH° | 10.3 ± 0.75 | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 88.7 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
ΔrS° | 100. | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase |
By formula: (O2+ • 4O2) + O2 = (O2+ • 5O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase |
ΔrH° | 8. ± 3. | kJ/mol | PHPMS | Conway and Janik, 1970 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 89.5 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
ΔrS° | 71.1 | J/mol*K | PHPMS | Conway and Janik, 1970 | gas phase |
By formula: (O2+ • 5O2) + O2 = (O2+ • 6O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 90.8 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
By formula: (O2+ • 6O2) + O2 = (O2+ • 7O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8. ± 2. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 91.6 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase |
By formula: (O2+ • 7O2) + O2 = (O2+ • 8O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.61 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | N/A | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated |
By formula: O2+ + O3 = (O2+ • O3)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 60.7 | kJ/mol | FA | Dotan, Davidson, et al., 1978 | gas phase; switching reaction(O2+)O2, Entropy change calculated or estimated; Conway and Janik, 1970 |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 85.8 | J/mol*K | N/A | Dotan, Davidson, et al., 1978 | gas phase; switching reaction(O2+)O2, Entropy change calculated or estimated; Conway and Janik, 1970 |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 35. | kJ/mol | FA | Dotan, Davidson, et al., 1978 | gas phase; switching reaction(O2+)O2, Entropy change calculated or estimated; Conway and Janik, 1970 |
References
Go To: Top, Ion clustering data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Hiraoka, Nakajima, et al., 1988
Hiraoka, K.; Nakajima, G.; Shoda, S.,
Determination of the Stabilities of CO2+(CO2)n and O2+(CO2)n Clusters with n = 1 - 6,
Chem. Phys. Lett., 1988, 146, 6, 535, https://doi.org/10.1016/0009-2614(88)87495-5
. [all data]
Illies, 1988
Illies, A.J.,
Thermochemistry of the Gas - Phase Ion - Molecule Clustering of CO2+CO2, SO2+CO2, N2O+N2O, O2+CO2, NO+CO2 and NO+N2O: Description of a New Hybrid Drift Tube/Ion Source with Coaxial Electron Beam and Ion Exit Apertures,
J. Phys. Chem., 1988, 92, 10, 2889, https://doi.org/10.1021/j100321a037
. [all data]
Dotan, Davidson, et al., 1978
Dotan, I.; Davidson, J.A.; Fehsenfeld, F.C.; Albritton, D.L.,
Reactions of O2+.O2 with CO2, O3 and CH4 and O2+.O3 with H2O and CH4 and their Role in Stratospheric Ion Chemistry,
J. Geophys. Res., 1978, 83, C8, 4036, https://doi.org/10.1029/JC083iC08p04036
. [all data]
Conway and Janik, 1970
Conway, D.C.; Janik, G.S.,
Determination of the Bond Energies for the Series O2 - O2+ through O2 - O10+,
J. Chem. Phys., 1970, 53, 5, 1859, https://doi.org/10.1063/1.1674262
. [all data]
Meot-Ner (Mautner) and Field, 1977
Meot-Ner (Mautner), M.; Field, F.H.,
Proton Affinity and Ion - Molecule Clustering in CO2 and CS2. Applications in Martian Ionospheric Chemistry,
J. Chem. Phys., 1977, 66, 10, 4527, https://doi.org/10.1063/1.433706
. [all data]
Rakshit and Warneck, 1981
Rakshit, A.B.; Warneck, P.,
Formation and Reactions of O2+.CO2, O2+.H2O and O2+(CO2)2 Ions,
Int. J. Mass Spectrom Ion Phys., 1981, 40, 2, 135, https://doi.org/10.1016/0020-7381(81)80037-X
. [all data]
Adams and Bohme, 1970
Adams, N.G.; Bohme, D.,
Flowing Afterglow Studies of Formation and Reactions of Cluster Ions of O2+, O2-, and O-,
J. Chem. Phys., 1970, 52, 6, 3133, https://doi.org/10.1063/1.1673449
. [all data]
Jarrold, Misev, et al., 1984
Jarrold, M.F.; Misev, L.; Bowers, M.T.,
Charge Transfer Half - Collisions: Photodissociation of the Kr.O2+ cluster Ion with Resolution of the Product Vibrational States,
J. Chem. Phys., 1984, 81, 10, 4369, https://doi.org/10.1063/1.447448
. [all data]
Hiraoka, Fujimaki, et al., 1994
Hiraoka, K.; Fujimaki, S.; Aruga, K.; Sato, T.; Yamabe, S.,
Gas-Phase Solavtion of NO+, O2+, N2O+, and H3O+ with N2O,
J. Chem. Phys., 1994, 101, 5, 4073, https://doi.org/10.1063/1.467524
. [all data]
Hiraoka and Nakajima, 1988
Hiraoka, K.; Nakajima, G.,
A Determination of the Stabilities of N2+(N2)n and O2+(N2)n with n = 1 - 11 from Measurements of the Gas - Phase Ion Equilibria,
J. Chem. Phys., 1988, 88, 12, 7709, https://doi.org/10.1063/1.454285
. [all data]
Speller and Fitaire, 1983
Speller, C.V.; Fitaire, M.,
Proceedings of the 16th International Conference on Phenomena of Ionized Gases, H. Boetticher, H. Wenk and E. Shulz - Gulde, ed(s)., ICPIG, Dusseldorf, 1983, 568. [all data]
Janik and Conway, 1967
Janik, G.S.; Conway, D.C.,
Bonding in Heteromolecular Ion Clusters. N2O2+,
J. Phys. Chem., 1967, 71, 4, 823, https://doi.org/10.1021/j100863a007
. [all data]
Howard, Bierbaum, et al., 1972
Howard, C.J.; Bierbaum, V.M.; Rundle, H.W.; Kaufman, F.,
Kinetics and Mechanism of Formation of Water Cluster Ions from O2+ and H2O+,
J. Chem. Phys., 1972, 57, 8, 3491, https://doi.org/10.1063/1.1678783
. [all data]
Hiraoka, 1988
Hiraoka, K.,
A Determination of the Stabilities of O2+(O2)n and O2-(O2)n with n = 1 - 8 from Measurements of the Gas-Phase Ion Equilibria,
J. Chem. Phys., 1988, 89, 5, 3190, https://doi.org/10.1063/1.454976
. [all data]
Durden, Kebarle, et al., 1969
Durden, D.A.; Kebarle, P.; Good, A.,
Thermal Ion-Molecule Reaction Rate Constants at Pressures up to 10 torr with a Pulsed Mass Spectrometer. Reactions in Methane, Krypton, and Oxygen,
J. Chem. Phys., 1969, 50, 2, 805, https://doi.org/10.1063/1.1671133
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Yang and Conway, 1964
Yang, J.H.; Conway, D.C.,
Bonding in Ion Clusters. I. O4+,
J. Chem. Phys., 1964, 40, 6, 1729, https://doi.org/10.1063/1.1725389
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Rakshit and Warneck, 1980
Rakshit, A.B.; Warneck, P.,
A Drift Chamber Study of the Formation of Water Cluster Ions in Oxygen,
J. Chem. Phys., 1980, 73, 10, 5074, https://doi.org/10.1063/1.439985
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Notes
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- Symbols used in this document:
T Temperature ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions ΔrS° Entropy of reaction at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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