Nitrogen
- Formula: N2
- Molecular weight: 28.0134
- IUPAC Standard InChIKey: IJGRMHOSHXDMSA-UHFFFAOYSA-N
- CAS Registry Number: 7727-37-9
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Nitrogen gas; N2; UN 1066; UN 1977; Dinitrogen; Molecular nitrogen; Diatomic nitrogen; Nitrogen-14
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Reaction thermochemistry data
Go To: Top, Henry's Law data, Gas phase ion energetics data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled as indicated in comments:
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
MS - José A. Martinho Simões
B - John E. Bartmess
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.
Reactions 1 to 50
By formula: NO- + N2 = (NO- • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 19. ± 1. | kJ/mol | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
ΔrH° | 20. | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; ΔrS+-12. J/mol*K; M |
ΔrH° | 18. | kJ/mol | HPMS | Speller, Fitaire, et al., 1983 | gas phase; Entropy change is questionable; M |
ΔrH° | 22. | kJ/mol | HPMS | Turner and Conway, 1976 | gas phase; M |
ΔrH° | 19. | kJ/mol | DT | Johnsen, Huang, et al., 1975 | gas phase; corrected for ln T by Keesee and Castleman, 1986; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 71.1 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
ΔrS° | 57.7 | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; ΔrS+-12. J/mol*K; M |
ΔrS° | 55.6 | J/mol*K | HPMS | Speller, Fitaire, et al., 1983 | gas phase; Entropy change is questionable; M |
ΔrS° | 79.1 | J/mol*K | HPMS | Turner and Conway, 1976 | gas phase; M |
ΔrS° | 65.7 | J/mol*K | DT | Johnsen, Huang, et al., 1975 | gas phase; corrected for ln T by Keesee and Castleman, 1986; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
2. | 200. | FA | Dunkin, Fehsenfeld, et al., 1971 | gas phase; M |
By formula: N2+ + N2 = (N2+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 102. to 102. | kJ/mol | RNG | N/A | Range of 6 values; Individual data points |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 87.9 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
ΔrS° | 67.8 | J/mol*K | PHPMS | Teng and Conway, 1973 | gas phase; M |
ΔrS° | 81.6 | J/mol*K | PHPMS | Payzant and Kebarle, 1970 | gas phase; M |
ΔrS° | 46. | J/mol*K | DT | Varney, 1968 | gas phase; Entropy change is questionable; M |
ΔrS° | -4. | J/mol*K | DT | Varney, 1959 | gas phase; Entropy change is questionable; M |
By formula: O2+ + N2 = (O2+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 21. ± 1. | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
ΔrH° | 22. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; M |
ΔrH° | 24. | kJ/mol | PHPMS | Janik and Conway, 1967 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 72.8 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
ΔrS° | 66.1 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; M |
ΔrS° | 79.1 | J/mol*K | PHPMS | Janik and Conway, 1967 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
0.0 | 296. | FA | Howard, Bierbaum, et al., 1972 | gas phase; M |
By formula: (HN2+ • 4N2) + N2 = (HN2+ • 5N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 12. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrH° | 13. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 95.8 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrS° | 84. | J/mol*K | N/A | Hiraoka, Saluja, et al., 1979 | gas phase; Entropy change calculated or estimated; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
5.9 | 92. | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; Entropy change calculated or estimated; M |
By formula: (O2- • 7N2 • O2) + N2 = (O2- • 8N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7. ± 1. | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrH° | 6.40 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 74.9 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
ΔrS° | 75.3 | J/mol*K | N/A | Hiraoka, 1988 | gas phase; Entropy change calculated or estimated; M |
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; M |
ΔrH° | 15. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 82.0 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
ΔrS° | 50.6 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
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; M |
ΔrH° | 18. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 79.9 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
ΔrS° | 57.7 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
By formula: (NO- • N2) + N2 = (NO- • 2N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 17. ± 1. | kJ/mol | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
ΔrH° | 16. | kJ/mol | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 72.8 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
ΔrS° | 52.7 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
C3N2NiO3 (solution) = C3NiO3 (solution) + (solution)
By formula: C3N2NiO3 (solution) = C3NiO3 (solution) + N2 (solution)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 42. ± 4. | kJ/mol | KinS | Turner, Simpson, et al., 1983 | solvent: Liquid krypton; The reaction enthalpy relies on the experimental value for the activation enthalpy, 42. ± 4. kJ/mol, and on the assumption that the activation enthalpy for product recombination is negligible Turner, Simpson, et al., 1983.; MS |
By formula: N+ + N2 = (N+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 249. | kJ/mol | N/A | National Bureau of Standards, 1968 | gas phase; from ΔrH(f); M |
ΔrH° | 250. | kJ/mol | EI | Saporoschenko, 1965 | gas phase; M |
ΔrH° | 250. | kJ/mol | EI | Franklin, Dibeler, et al., 1958 | gas phase; M |
Enthalpy of reaction
ΔrH° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
361. (+7.5,-0.) | CID | Haynes, Freysinger, et al., 1995 | gas phase; guided ion beam CID; M |
By formula: Cu+ + N2 = (Cu+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 26. | kJ/mol | HPMS | El-Shall, Schriver, et al., 1989 | gas phase; Cu+ from laser desrption; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67. | J/mol*K | HPMS | El-Shall, Schriver, et al., 1989 | gas phase; Cu+ from laser desrption; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 5.9 | kJ/mol | HPMS | El-Shall, Schriver, et al., 1989 | gas phase; Cu+ from laser desrption; M |
By formula: (HN2+ • 2N2) + N2 = (HN2+ • 3N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 14. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrH° | 16. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84.1 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrS° | 84. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
By formula: (HN2+ • 3N2) + N2 = (HN2+ • 4N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 14. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrH° | 15. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 88.7 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrS° | 84. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
By formula: (HN2+ • N2) + N2 = (HN2+ • 2N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 15. ± 1. | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrH° | 17. | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 80.3 | J/mol*K | PHPMS | Hiraoka and Mori, 1989 | gas phase; M |
ΔrS° | 75. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
By formula: Na+ + N2 = (Na+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 33. | kJ/mol | FA | Perry, Rowe, et al., 1980 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 77.8 | J/mol*K | FA | Perry, Rowe, et al., 1980 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
9.2 | 310. | FA | Perry, Rowe, et al., 1980 | gas phase; M |
8.4 | 310. | DT | Beyer and Keller, 1971 | gas phase; low E/N; M |
By formula: HN2+ + N2 = (HN2+ • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 66.9 | kJ/mol | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
ΔrH° | 60.7 | kJ/mol | PHPMS | Meot-Ner (Mautner) and Field, 1974 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 100. | J/mol*K | PHPMS | Hiraoka, Saluja, et al., 1979 | gas phase; M |
ΔrS° | 85.4 | J/mol*K | PHPMS | Meot-Ner (Mautner) and Field, 1974 | gas phase; M |
C39H66N2O3P2W (solution) + (g) = C39H68O3P2W (solution) + (g)
By formula: C39H66N2O3P2W (solution) + H2 (g) = C39H68O3P2W (solution) + N2 (g)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 18.4 ± 1.7 | kJ/mol | EqS | Gonzalez and Hoff, 1989 | solvent: Tetrahydrofuran; Temperature range: 288-308 K; MS |
C39H66MoO3P3 (solution) + (g) = C39H66MoN2O3P2 (solution)
By formula: C39H66MoO3P3 (solution) + N2 (g) = C39H66MoN2O3P2 (solution)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -37.7 ± 2.5 | kJ/mol | EqS | Gonzalez and Hoff, 1989 | solvent: Tetrahydrofuran; Temperature range: 294-308 K; MS |
By formula: (H3O+ • 2N2 • 3H2O) + N2 = (H3O+ • 3N2 • 3H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 5.0 | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; ΔrH, ΔrS approximate; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 27. | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; ΔrH, ΔrS approximate; M |
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; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 67.8 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
3. | 184. | HPMS | Speller and Fitaire, 1983 | gas phase; M |
By formula: (NO- • 2N2) + N2 = (NO- • 3N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 16. ± 1. | kJ/mol | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 70.3 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
4. | 204. | HPMS | Speller, Fitaire, et al., 1983 | gas phase; M |
By formula: (NO- • 3N2) + N2 = (NO- • 4N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 14. ± 1. | kJ/mol | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 74.9 | J/mol*K | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
2. | 204. | HPMS | Speller, Fitaire, et al., 1983 | gas phase; M |
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; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 94.1 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
3. | 204. | HPMS | Speller and Fitaire, 1983 | gas phase; M |
By formula: (H3O+ • 3N2 • 2H2O) + N2 = (H3O+ • 4N2 • 2H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10. | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; ΔrH, ΔrS approximate; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 50. | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; ΔrH, ΔrS approximate; M |
By formula: (NO- • 9N2) + N2 = (NO- • 10N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.03 | kJ/mol | PHPMS | Hiraoka and Yamabe, 1989 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 79. | J/mol*K | N/A | Hiraoka and Yamabe, 1989 | gas phase; Entropy change calculated or estimated; M |
By formula: (HN2+ • 10N2) + N2 = (HN2+ • 11N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.20 | kJ/mol | PHPMS | Hiraoka and Mori, 1989 | gas phase; Entropy change calculated or estimated; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | N/A | Hiraoka and Mori, 1989 | gas phase; Entropy change calculated or estimated; M |
By formula: O3- + N2 = (O3- • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.3 ± 0.84 | kJ/mol | TDAs | Hiraoka, 1988 | gas phase; B,M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 77.0 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | -11.7 ± 2.1 | kJ/mol | TDAs | Hiraoka, 1988 | gas phase; B |
By formula: (C2H5+ • N2) + N2 = (C2H5+ • 2N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 19. | kJ/mol | HPMS | Speller, 1983 | gas phase; deuterated, Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 45.6 | J/mol*K | HPMS | Speller, 1983 | gas phase; deuterated, Entropy change is questionable; M |
By formula: (N2+ • N2) + N2 = (N2+ • 2N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.5 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
ΔrH° | 5.9 | kJ/mol | PI | Linn, Ono, et al., 1981 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 62.8 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
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; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 42.3 | J/mol*K | HPMS | Speller and Fitaire, 1983 | gas phase; Entropy change is questionable; M |
By formula: (Na+ • N2) + N2 = (Na+ • 2N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 22. | kJ/mol | FA | Perry, Rowe, et al., 1980 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 70.3 | J/mol*K | FA | Perry, Rowe, et al., 1980 | gas phase; M |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
-1. | 310. | FA | Perry, Rowe, et al., 1980 | gas phase; M |
By formula: (CH2N+ • 2N2) + N2 = (CH2N+ • 3N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 13. | kJ/mol | HPMS | Speller, Fitaire, et al., 1982 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 54.8 | J/mol*K | HPMS | Speller, Fitaire, et al., 1982 | gas phase; Entropy change is questionable; M |
By formula: (CH2N+ • 3N2) + N2 = (CH2N+ • 4N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 13. | kJ/mol | HPMS | Speller, Fitaire, et al., 1982 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 57.7 | J/mol*K | HPMS | Speller, Fitaire, et al., 1982 | gas phase; Entropy change is questionable; M |
By formula: (CH2N+ • 4N2) + N2 = (CH2N+ • 5N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 13. | kJ/mol | HPMS | Speller, Fitaire, et al., 1982 | gas phase; Entropy change is questionable; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 63.6 | J/mol*K | HPMS | Speller, Fitaire, et al., 1982 | gas phase; Entropy change is questionable; M |
By formula: C4H4BrNO2 + 0.5H4N2 = HBr + C4H5NO2 + 0.5N2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | -260.3 ± 0.46 | kJ/mol | Cm | Howard and Skinner, 1966 | solid phase; solvent: Aqueous solution; Reanalyzed by Pedley, Naylor, et al., 1986, Original value = -261.7 ± 0.46 kJ/mol; ALS |
By formula: O2- + N2 = (O2- • N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 25. ± 4.2 | kJ/mol | N/A | Posey and Johnson, 1988 | gas phase; B |
ΔrH° | <56.90 | kJ/mol | IMRB | Adams and Bohme, 1970 | gas phase; N2..O2- + O2 -> O4-; B |
C12H34P4Ru (solution) + (solution) = C12H32N2P4Ru (solution) + (solution)
By formula: C12H34P4Ru (solution) + N2 (solution) = C12H32N2P4Ru (solution) + H2 (solution)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 16.3 | kJ/mol | PAC | Belt, Scaiano, et al., 1993 | solvent: Cyclohexane; The reaction enthalpy relies on 0.85 for the quantum yield of H2 dissociation.; MS |
By formula: (H3O+ • 2N2 • 2H2O) + N2 = (H3O+ • 3N2 • 2H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 38. ± 11. | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 119. | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; M |
(solution) + (solution) = C8H5N2O3V (solution) + (solution)
By formula: C9H5O4V (solution) + N2 (solution) = C8H5N2O3V (solution) + CO (solution)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 27. ± 4. | kJ/mol | PAC | Johnson, Popov, et al., 1991 | solvent: Heptane; The reaction enthalpy relies on 0.80 for the quantum yield of CO dissociation.; MS |
By formula: (O2- • 2N2 • O2) + N2 = (O2- • 3N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 10.3 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 76.6 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 3N2 • O2) + N2 = (O2- • 4N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 9.0 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.2 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 4N2 • O2) + N2 = (O2- • 5N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 8.1 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 81.6 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 5N2 • O2) + N2 = (O2- • 6N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.6 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 81.6 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • 6N2 • O2) + N2 = (O2- • 7N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 7.1 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 78.7 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (O2- • N2 • O2) + N2 = (O2- • 2N2 • O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 11.7 ± 0.8 | kJ/mol | PHPMS | Hiraoka, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 74.9 | J/mol*K | PHPMS | Hiraoka, 1988 | gas phase; M |
By formula: (H3O+ • 2N2 • H2O) + N2 = (H3O+ • 3N2 • H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 33. ± 8. | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 92. | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; M |
By formula: (H3O+ • N2 • 2H2O) + N2 = (H3O+ • 2N2 • 2H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 22. | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 69.5 | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; M |
By formula: (H3O+ • N2 • 3H2O) + N2 = (H3O+ • 2N2 • 3H2O)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 18. | kJ/mol | DT | Gheno and Fitaire, 1987 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 65.7 | J/mol*K | DT | Gheno and Fitaire, 1987 | gas phase; M |
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; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84.5 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
By formula: (N2+ • 10N2) + N2 = (N2+ • 11N2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 6.9 ± 0.8 | kJ/mol | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
Quantity | Value | Units | Method | Reference | Comment |
ΔrS° | 84.5 | J/mol*K | PHPMS | Hiraoka and Nakajima, 1988 | gas phase; M |
Henry's Law data
Go To: Top, Reaction thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), 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: Rolf Sander
Henry's Law constant (water solution)
kH(T) = k°H exp(d(ln(kH))/d(1/T) ((1/T) - 1/(298.15 K)))
k°H = Henry's law constant for solubility in water at 298.15 K (mol/(kg*bar))
d(ln(kH))/d(1/T) = Temperature dependence constant (K)
k°H (mol/(kg*bar)) | d(ln(kH))/d(1/T) (K) | Method | Reference |
---|---|---|---|
0.00060 | 1300. | X | N/A |
0.00065 | 1300. | L | N/A |
Gas phase ion energetics data
Go To: Top, Reaction thermochemistry data, Henry's Law data, Mass spectrum (electron ionization), References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias
L - Sharon G. Lias
Data compiled as indicated in comments:
LL - Sharon G. Lias and Joel F. Liebman
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
View reactions leading to N2+ (ion structure unspecified)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 15.581 ± 0.008 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 493.8 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 464.5 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
15.581 ± 0.008 | S | Trickl, Cromwell, et al., 1989 | LL |
15.7 ± 0.1 | EI | Stephen, Mark, et al., 1984 | LBLHLM |
15.6 ± 0.1 | EI | Grade, Wienecke, et al., 1983 | LBLHLM |
15.60 | PE | Kimura, Katsumata, et al., 1981 | LLK |
10.1 ± 0.6 | EI | Armentrout, Tarr, et al., 1981 | LLK |
15.58 | EI | Armentrout, Tarr, et al., 1981 | LLK |
15.5808 | EVAL | Huber and Herzberg, 1979 | LLK |
15.58 ± 0.02 | EI | Sahini, Constantin, et al., 1978 | LLK |
15.5 | PI | Rabalais, Debies, et al., 1974 | LLK |
15.58 | PE | Lee and Rabalais, 1974 | LLK |
15.61 | PE | Natalis, 1973 | LLK |
15.58 ± 0.01 | PE | Hotop and Niehaus, 1970 | RDSH |
15.56 | CI | Cermak, 1968 | RDSH |
15.58 | PI | Cook and Metzger, 1964 | RDSH |
15.5803 | S | Ogawa and Tanaka, 1962 | RDSH |
15.5802 | S | Worley, 1943 | RDSH |
15.5812 ± 0.0002 | S | Worley and Jenkins, 1938 | RDSH |
15.58 | PE | Potts and Williams, 1974 | Vertical value; LLK |
15.60 | PE | Katrib, Debies, et al., 1973 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
N+ | 24.34 | N(4So) | EI | Locht, Schopman, et al., 1975 | LLK |
N+ | 24.3 | N | EI | Smyth, Schiavone, et al., 1973 | LLK |
N+ | 24.4 ± 0.25 | N | EI | Crowe and McConkey, 1973 | LLK |
N+ | 24.32 ± 0.03 | N | EI | Hierl and Franklin, 1967 | RDSH |
N+ | 48. ± 2. | N+ | EI | Hierl and Franklin, 1967 | RDSH |
N+ | 24.32 ± 0.02 | N | EI | Frost and McDowell, 1956 | RDSH |
Mass spectrum (electron ionization)
Go To: Top, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, 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: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
Origin | D.HENNEBERG, MAX-PLANCK INSTITUTE, MULHEIM, WEST GERMANY |
NIST MS number | 61309 |
References
Go To: Top, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Hiraoka and Yamabe, 1989
Hiraoka, K.; Yamabe, S.,
How are Nitrogen Molecules Bound to NO2+ and NO+?,
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Ion - Molecule Equilibria in Mixtures of N2 and Ar,
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Clustering Equilibrium N2+ + 2N2 = N4+ + N2 and the Bond Dissociation Energy of N4+,
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Varney, 1968
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Equilibrium Constant and Rates for the Reversible Reaction N4+ -> N2+ + N2,
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Molecular Ions,
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Bonding in Heteromolecular Ion Clusters. N2O2+,
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Howard, C.J.; Bierbaum, V.M.; Rundle, H.W.; Kaufman, F.,
Kinetics and Mechanism of Formation of Water Cluster Ions from O2+ and H2O+,
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Hiraoka and Mori, 1989
Hiraoka, K.; Mori, T.,
Gas Phase Stabilities of the Cluster Ions H+(CO)2(CO)n, H+(N2)2(N2)n and H+(O2)2(O2)n with n = 1 - 14,
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. [all data]
Hiraoka, Saluja, et al., 1979
Hiraoka, K.; Saluja, P.P.S.; Kebarle, P.,
Stabilities of Complexes (N2)nH+, (CO)nH+ and (O2)nH+ for n = 1 to 7 Based on Gas Phase Ion Equilibrium Measurements,
Can. J. Chem., 1979, 57, 16, 2159, https://doi.org/10.1139/v79-346
. [all data]
Hiraoka, 1988
Hiraoka, K.,
Determination of the Stabilities of O3-(N2)n, O3-(O2)n, and O4-(N2)n from Measurements of the Gas Phase Equilibria,
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. [all data]
Turner, Simpson, et al., 1983
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National Bureau of Standards, 1968
National Bureau of Standards, US,
Technical Note 270 - 3
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Saporoschenko, 1965
Saporoschenko, M.,
Mobility of Mass Analyzed N+, N2+, N3+, and N4+ Ions in Nitrogen Gas,
Phys. Rev. A, 1965, 139, 352. [all data]
Franklin, Dibeler, et al., 1958
Franklin, J.L.; Dibeler, V.H.; Reese, R.M.; Krauss, M.,
Ionization and dissociation of hydrazoic acid and methyl azide by electron impact,
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Haynes, Freysinger, et al., 1995
Haynes, C.L.; Freysinger, W.; Armentrout, P.B.,
Collision-induced dissociation of N3+(X3-) with Ne, Ar, Kr, and Xe,
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El-Shall, Schriver, et al., 1989
El-Shall, M.S.; Schriver, K.E.; Whetten, R.L.; Meot-Ner (Mautner), M.,
Ion/Molecule Clustering Thermochemistry by Laser Ionization High - Pressure Mass Spectrometry,
J. Phys. Chem., 1989, 93, 24, 7969, https://doi.org/10.1021/j100361a002
. [all data]
Perry, Rowe, et al., 1980
Perry, R.A.; Rowe, B.R.; Viggiano, A.A.; Albritton, D.L.; Ferguson, E.E.; Fehsenfeld, F.C.,
Laboratory Measurements of Stratospheric Sodium Ion Measurements,
Geophys. Res. Lett., 1980, 7, 9, 693, https://doi.org/10.1029/GL007i009p00693
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Beyer and Keller, 1971
Beyer, R.A.; Keller, G.E.,
The Clustering of Atmospheric Gases to Alkali Ions,
Trans. Am. Geophys. Union, 1971, 52, 303. [all data]
Meot-Ner (Mautner) and Field, 1974
Meot-Ner (Mautner), M.; Field, F.H.,
Kinetics and Thermodynamics of the Association of CO+ with CO and of N2+ with N2 between 120 and 650 K,
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Gonzalez and Hoff, 1989
Gonzalez, A.A.; Hoff, C.D.,
Inorg. Chem., 1989, 28, 4295. [all data]
Speller, 1983
Speller, C.V.,
Ph. D. Thesis, Universite de Paris Sud, 1983. [all data]
Linn, Ono, et al., 1981
Linn, S.H.; Ono, Y.; Ng, C.Y.,
Molecular Beam Photoionization Study of CO, N2, and NO Dimers and Clusters,
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. [all data]
Speller, Fitaire, et al., 1982
Speller, C.V.; Fitaire, M.; Pointu, A.M.,
H2CN+.nN2 Clustering Formation and the Atmosphere of Titan,
Nature, 1982, 300, 5892, 507, https://doi.org/10.1038/300507a0
. [all data]
Howard and Skinner, 1966
Howard, P.B.; Skinner, H.A.,
Thermochemistry of some reactions of aqueous hydrazine with halogens, hydrogen halides and N-halogenosuccinimides,
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Pedley, Naylor, et al., 1986
Pedley, J.B.; Naylor, R.D.; Kirby, S.P.,
Thermochemical Data of Organic Compounds, Chapman and Hall, New York, 1986, 1-792. [all data]
Posey and Johnson, 1988
Posey, L.A.; Johnson, M.A.,
Pulsed Photoelectron Spectroscopy of Negative Cluster Ions: Isolation of Three Distinguishable Forms of N2O2-,
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Adams and Bohme, 1970
Adams, N.G.; Bohme, D.,
Flowing Afterglow Studies of Formation and Reactions of Cluster Ions of O2+, O2-, and O-,
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Belt, Scaiano, et al., 1993
Belt, S.T.; Scaiano, J.C.; Whittlesey, M.K.,
J. Am. Chem. Soc., 1993, 115, 1921. [all data]
Johnson, Popov, et al., 1991
Johnson, F.P.A.; Popov, V.K.; George, M.W.; Bagratashvili, V.N.; Poliakoff, M.; Turner, J.J.,
Mendeleev Commun., 1991, 145.. [all data]
Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G.,
Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update,
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. [all data]
Trickl, Cromwell, et al., 1989
Trickl, T.; Cromwell, E.F.; Lee, Y.T.; Kung, A.H.,
State-selective ionization of nitrogen in the X2 =0 and v =1 states by two-color (1+1) photon excitation near threshold,
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Stephen, Mark, et al., 1984
Stephen, K.; Mark, T.D.; Futrell, J.H.; Helm, H.,
Electron impact ionization of (N2)2: Appearance energies of N3+ and N4+,
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Grade, Wienecke, et al., 1983
Grade, M.; Wienecke, J.; Rosinger, W.; Hirschwald, W.,
Electron impact investigation of the molecules SeS(g) and TeSe(g) under high-temperature equilibrium conditions,
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Kimura, Katsumata, et al., 1981
Kimura, K.; Katsumata, S.; Achiba, Y.; Yamazaki, T.; Iwata, S.,
Ionization energies, Ab initio assignments, and valence electronic structure for 200 molecules
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Armentrout, Tarr, et al., 1981
Armentrout, P.B.; Tarr, S.M.; Dori, A.; Freund, R.S.,
Electron impact ionization cross section of metastable N2 (A2Σu+),
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Huber and Herzberg, 1979
Huber, K.P.; Herzberg, G.,
Molecular Spectra and Molecular Structure. IV. Constants of Diatomic Molecules,, Van Nostrand Reinhold Co., 1979, ,1. [all data]
Sahini, Constantin, et al., 1978
Sahini, V.E.; Constantin, V.; Serban, I.,
Determination of ionization potentials using a MI-1305 mass spectrometer,
Rev. Roum. Chim., 1978, 23, 479. [all data]
Rabalais, Debies, et al., 1974
Rabalais, J.W.; Debies, T.P.; Berkosky, J.L.; Huang, J.-T.J.; Ellison, F.O.,
Calculated photoionization cross sections relative experimental photoionization intensities for a selection of small molecules,
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Lee and Rabalais, 1974
Lee, T.H.; Rabalais, J.W.,
Vibrational transition probabilities in photoelectron spectra,
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Natalis, 1973
Natalis, P.,
Contribution a la spectroscopie photoelectronique. Effets de l'autoionisation dans less spectres photoelectroniques de molecules diatomiques et triatomiques,
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Hotop and Niehaus, 1970
Hotop, H.; Niehaus, A.,
Reactions of excited atoms and molecules with atoms and molecules. V.Comparison of Penning electron and photoelectron spectra of H2, N2 and CO,
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Cermak, 1968
Cermak, V.,
Penning ionization electron spectroscopy. I. Determination of ionization potentials of polyatomic molecules,
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Cook and Metzger, 1964
Cook, G.R.; Metzger, P.H.,
Photoionization and absorption cross sections of O2 and N2 in the 600- to 1000-A region,
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Ogawa and Tanaka, 1962
Ogawa, M.; Tanaka, Y.,
Rydberg absorption series of N2,
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Worley, 1943
Worley, R.E.,
Absorption spectrum of N2 in the extreme ultraviolet,
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Worley and Jenkins, 1938
Worley, R.E.; Jenkins, F.A.,
A new Rydberg series in N2,
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Potts and Williams, 1974
Potts, A.W.; Williams, T.A.,
The observation of "forbidden" transitions in He II photoelectron spectra,
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Katrib, Debies, et al., 1973
Katrib, A.; Debies, T.P.; Colton, R.J.; Lee, T.H.; Rabalais, J.W.,
The use of differential photoionization cross sections as a function of excitation energy in assigning photoelectron spectra,
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Locht, Schopman, et al., 1975
Locht, R.; Schopman, J.; Wankenne, H.; Momigny, J.,
The dissociative ionization of nitrogen,
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Smyth, Schiavone, et al., 1973
Smyth, K.C.; Schiavone, J.A.; Freund, R.S.,
Dissociative excitation of N2 by electron impact: Translational spectroscopy of long-lived high- Rydberg fragment atoms,
J. Chem. Phys., 1973, 59, 5225. [all data]
Crowe and McConkey, 1973
Crowe, A.; McConkey, J.W.,
Dissociative ionization by electron impact II. N+ N++ from N2,
J. Phys. B:, 1973, 6, 2108. [all data]
Hierl and Franklin, 1967
Hierl, P.M.; Franklin, J.L.,
Appearance potentials and kinetic energies of ions from N2, CO, and NO,
J. Chem. Phys., 1967, 47, 3154. [all data]
Frost and McDowell, 1956
Frost, D.C.; McDowell, C.A.,
The dissociation energy of the nitrogen molecule,
Proc. Roy. Soc. (London), 1956, A236, 278. [all data]
Notes
Go To: Top, Reaction thermochemistry data, Henry's Law data, Gas phase ion energetics data, Mass spectrum (electron ionization), References
- Symbols used in this document:
AE Appearance energy IE (evaluated) Recommended ionization energy T Temperature d(ln(kH))/d(1/T) Temperature dependence parameter for Henry's Law constant k°H Henry's Law constant at 298.15K 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
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
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