Selected ATcT [1, 2] enthalpy of formation based on version 1.140 of the Thermochemical Network [3]

This version of ATcT results[3] was generated by additional expansion of version 1.130 to fully include the highest-level electronic structure computations described in reference [4].

Oxygen atom cation

Formula: O+ (g)

CAS RN: 14581-93-2

ATcT ID: 14581-93-2*0

SMILES: [O+]

InChI: InChI=1S/O/q+1

InChIKey: KLZXPVWVDXGFTD-UHFFFAOYSA-N

Hills Formula: O1+

2D Image:

Aliases: O+; Oxygen atom cation; Oxygen atom ion (1+); Atomic oxygen cation; Atomic oxygen ion (1+); Monooxygen cation; Monooxygen ion (1+); Monoxygen cation; Monoxygen ion (1+); Oxygen cation; Oxygen ion (1+)

Relative Molecular Mass: 15.99885 ± 0.00030

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
1560.786	1562.643	± 0.0021	kJ/mol

3D Image of O+ (g)

spin ON spin OFF

Top contributors to the provenance of Δ_fH° of O+ (g)

The 5 contributors listed below account for 96.7% of the provenance of Δ_fH° of O+ (g).

Please note: The list is limited to 20 most important contributors or, if less, a number sufficient to account for 90% of the provenance. The Reference acts as a further link to the relevant references and notes for the measurement. The Measured Quantity is normaly given in the original units; in cases where we have reinterpreted the original measurement, the listed value may differ from that given by the authors. The quoted uncertainty is the a priori uncertainty used as input when constructing the initial Thermochemical Network, and corresponds either to the value proposed by the original authors or to our estimate; if an additional multiplier is given in parentheses immediately after the prior uncertainty, it corresponds to the factor by which the prior uncertainty needed to be multiplied during the ATcT analysis in order to make that particular measurement consistent with the prevailing knowledge contained in the Thermochemical Network.

Contribution (%)	TN ID	Reaction	Measured Quantity	Reference
42.4	1.4	O2 (g) → 2 O (g)	Δ_rH°(0 K) = 41269.2 ± 0.5 cm-1	Lewis 1985, note O2b
24.0	24.2	O2 (g) → O+ (g) + O- (g)	Δ_rH°(0 K) = 139321.2 ± 0.7 cm-1	Martin 1997, note O2c
13.1	1.5	O2 (g) → 2 O (g)	Δ_rH°(0 K) = 41269.6 ± 0.9 cm-1	Gibson 1991, note O2b
8.7	1.6	O2 (g) → 2 O (g)	Δ_rH°(0 K) = 41268.6 ± 1.1 cm-1	Cosby 1992, note O2b
8.2	16.1	O (g) → O+ (g)	Δ_rH°(0 K) = 109837.02 ± 0.06 cm-1	Eriksson 1968, Moore 1970, NIST Atomic Web

Top 10 species with enthalpies of formation correlated to the Δ_fH° of O+ (g)

Please note: The correlation coefficients are obtained by renormalizing the off-diagonal elements of the covariance matrix by the corresponding variances.
The correlation coefficient is a number from -1 to 1, with 1 representing perfectly correlated species, -1 representing perfectly anti-correlated species, and 0 representing perfectly uncorrelated species.

Correlation Coefficent (%)	Species Name	Formula	Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units	Relative Molecular Mass	ATcT ID
94.3	Oxygen atom	O (g)	246.844	249.229	± 0.0021	kJ/mol	15.99940 ± 0.00030	17778-80-2*0
94.3	Oxygen atom	O (g, triplet)	246.844	249.229	± 0.0021	kJ/mol	15.99940 ± 0.00030	17778-80-2*1
94.3	Oxygen atom anion	O- (g)	105.868	108.097	± 0.0021	kJ/mol	15.99995 ± 0.00030	14337-01-0*0
94.3	Oxygen atom	O (g, singlet)	436.665	438.523	± 0.0021	kJ/mol	15.99940 ± 0.00030	17778-80-2*2
17.7	Oxygen atom dication	[O]+2 (g)	4949.458	4953.000	± 0.013	kJ/mol	15.99830 ± 0.00030	14127-63-0*0
12.6	Oxygen atom trication	[O]+3 (g)	10249.929	10252.880	± 0.018	kJ/mol	15.99775 ± 0.00030	14127-64-1*0
8.9	Oxygen atom tetracation	[O]+4 (g)	17719.207	17721.064	± 0.025	kJ/mol	15.99721 ± 0.00030	14127-65-2*0
7.8	Oxidanylium	[OH]+ (g)	1293.362	1293.391	± 0.025	kJ/mol	17.00679 ± 0.00031	12259-29-9*0
5.6	Nitrogen dioxide	ONO (g)	36.872	34.065	± 0.066	kJ/mol	46.00554 ± 0.00060	10102-44-0*0
5.5	Chlorooxidanyl	ClO (g)	101.124	101.716	± 0.035	kJ/mol	51.45210 ± 0.00095	14989-30-1*0

Most Influential reactions involving O+ (g)

Please note: The list, which is based on a hat (projection) matrix analysis, is limited to no more than 20 largest influences.

Influence Coefficient	TN ID	Reaction	Measured Quantity	Reference
0.999	26.1	O+ (g) → [O]+2 (g)	Δ_rH°(0 K) = 283270.9 ± 1 cm-1	NIST Atomic Web, est unc
0.993	16.1	O (g) → O+ (g)	Δ_rH°(0 K) = 109837.02 ± 0.06 cm-1	Eriksson 1968, Moore 1970, NIST Atomic Web
0.895	175.1	[OH]+ (g) → O+ (g) + H (g)	Δ_rH°(0 K) = 40412.0 ± 2.2 cm-1	Moselhy 1975, note unc
0.247	24.2	O2 (g) → O+ (g) + O- (g)	Δ_rH°(0 K) = 139321.2 ± 0.7 cm-1	Martin 1997, note O2c
0.057	256.2	[(HOH)O]+ (g) → H2O (g) + O+ (g)	Δ_rH°(0 K) = 39.75 ± 3.20 kcal/mol	Ruscic G4
0.052	256.4	[(HOH)O]+ (g) → H2O (g) + O+ (g)	Δ_rH°(0 K) = 36.99 ± 3.20 (×1.044) kcal/mol	Ruscic CBS-n
0.049	256.1	[(HOH)O]+ (g) → H2O (g) + O+ (g)	Δ_rH°(0 K) = 39.90 ± 3.44 kcal/mol	Ruscic G3X
0.046	2194.7	CO2 (g) → CO (g) + O+ (g)	Δ_rH°(0 K) = 19.0701 ± 0.0010 (×1.164) eV	Liu 2003, note unc
0.031	256.3	[(HOH)O]+ (g) → H2O (g) + O+ (g)	Δ_rH°(0 K) = 42.02 ± 4.32 kcal/mol	Ruscic CBS-n
0.017	1430.2	[NNN]+ (g) + [CO]+ (g) + O+ (g) → [CO2]+ (g) + [N2]+ (g) + N+ (g)	Δ_rH°(0 K) = -1.70 ± 1.60 kcal/mol	Ruscic G4
0.017	1430.3	[NNN]+ (g) + [CO]+ (g) + O+ (g) → [CO2]+ (g) + [N2]+ (g) + N+ (g)	Δ_rH°(0 K) = -2.15 ± 1.60 kcal/mol	Ruscic CBS-n
0.017	1430.4	[NNN]+ (g) + [CO]+ (g) + O+ (g) → [CO2]+ (g) + [N2]+ (g) + N+ (g)	Δ_rH°(0 K) = 0.11 ± 1.50 (×1.067) kcal/mol	Ruscic W1RO
0.015	1430.1	[NNN]+ (g) + [CO]+ (g) + O+ (g) → [CO2]+ (g) + [N2]+ (g) + N+ (g)	Δ_rH°(0 K) = -1.49 ± 1.72 kcal/mol	Ruscic G3X
0.003	23.6	O2 (g) → O+ (g) + O (g)	Δ_rH°(0 K) = 151100.4 ± 2.6 (×2.181) cm-1	note O2+f, Kong 1996, Cosby 1980, Pernot 1979
0.003	23.4	O2 (g) → O+ (g) + O (g)	Δ_rH°(0 K) = 151111 ± 6 cm-1	Cosby 1992, note O2+e, Yoshino 1968, Cosby 1980, Pernot 1979
0.002	2194.2	CO2 (g) → CO (g) + O+ (g)	Δ_rH°(0 K) = 19.071 ± 0.005 eV	Eland 1977, est unc
0.002	2194.3	CO2 (g) → CO (g) + O+ (g)	Δ_rH°(0 K) = 19.067 ± 0.005 eV	Kronebusch 1976, est unc
0.001	23.5	O2 (g) → O+ (g) + O (g)	Δ_rH°(0 K) = 151105.9 ± 9.2 cm-1	note O2+f, Kong 1996, Tadjeddine 1978, Albritton 1977
0.001	23.1	O2 (g) → O+ (g) + O (g)	Δ_rH°(0 K) = 151100.2 ± 9.2 cm-1	Albritton 1978, note O2+b, Yoshino 1968, Tadjeddine 1978, Albritton 1977
0.001	24.1	O2 (g) → O+ (g) + O- (g)	Δ_rH°(0 K) = 139316.6 ± 9.7 cm-1	Dehmer 1975, note O2+

References

1		B. Ruscic, R. E. Pinzon, M. L. Morton, G. von Laszewski, S. Bittner, S. G. Nijsure, K. A. Amin, M. Minkoff, and A. F. Wagner, Introduction to Active Thermochemical Tables: Several "Key" Enthalpies of Formation Revisited. J. Phys. Chem. A 108, 9979-9997 (2004) [DOI: 10.1021/jp047912y]
2		B. Ruscic, R. E. Pinzon, G. von Laszewski, D. Kodeboyina, A. Burcat, D. Leahy, D. Montoya, and A. F. Wagner, Active Thermochemical Tables: Thermochemistry for the 21^st Century. J. Phys. Conf. Ser. 16, 561-570 (2005) [DOI: 10.1088/1742-6596/16/1/078]
3		B. Ruscic and D. H. Bross, Active Thermochemical Tables (ATcT) values based on ver. 1.140 of the Thermochemical Network (2024); available at ATcT.anl.gov
4		J. H. Thorpe, J. L. Kilburn, D. Feller, P. B. Changala, D. H. Bross, B. Ruscic, and J. F. Stanton, Elaborated Thermochemical Treatment of HF, CO, N2, and H2O: Insight into HEAT and Its Extensions J. Chem. Phys. 155, 184109 (2021) [DOI: 10.1063/5.0069322]
5		B. Ruscic, Uncertainty Quantification in Thermochemistry, Benchmarking Electronic Structure Computations, and Active Thermochemical Tables. Int. J. Quantum Chem. 114, 1097-1101 (2014) [DOI: 10.1002/qua.24605]
6		B. Ruscic and D. H. Bross, Thermochemistry Computer Aided Chem. Eng. 45, 3-114 (2019) [DOI: 10.1016/B978-0-444-64087-1.00001-2]

Formula

The aggregate state is given in parentheses following the formula, such as: g - gas-phase, cr - crystal, l - liquid, etc.

Uncertainties

The listed uncertainties correspond to estimated 95% confidence limits, as customary in thermochemistry (see, for example, Ruscic [5] and Ruscic and Bross[6]).
Note that an uncertainty of ± 0.000 kJ/mol indicates that the estimated uncertainty is < ± 0.000₅ kJ/mol.

Website Functionality Credits

The reorganization of the website was developed and implemented by David H. Bross (ANL).
The find function is based on the complete Species Dictionary entries for the appropriate version of the ATcT TN.
The molecule images are rendered by Indigo-depict.
The XYZ renderings are based on Jmol: an open-source Java viewer for chemical structures in 3D. http://www.jmol.org/.

Acknowledgement

This work was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences and Biosciences under Contract No. DE-AC02-06CH11357.