Selected ATcT [1, 2] enthalpy of formation based on version 1.148 of the Thermochemical Network [3]

This version of ATcT results[3] was generated by additional expansion of version 1.140 to include species relevant to a recent study of the role of atmospheric methanediol[4].

Nitric oxide

Formula: NO (g)

CAS RN: 10102-43-9

ATcT ID: 10102-43-9*0

SMILES: [N]=O

InChI: InChI=1S/NO/c1-2

InChIKey: MWUXSHHQAYIFBG-UHFFFAOYSA-N

Hills Formula: N1O1

2D Image:

Aliases: NO; Nitric oxide; Oxoamino; Nitrogen oxide; Nitrogen monoxide; Nitrosyl radical; Oxoamidogen; Nitrogen (II) oxide; Nitrogen protoxide; N=O

Relative Molecular Mass: 30.00614 ± 0.00031

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
90.636	91.140	± 0.065	kJ/mol

3D Image of NO (g)

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Top contributors to the provenance of Δ_fH° of NO (g)

The 20 contributors listed below account only for 82.4% of the provenance of Δ_fH° of NO (g).
A total of 43 contributors would be needed to account for 90% of the provenance.

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
23.3	1467.1	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52400 ± 10 cm-1	Callear 1970
23.3	1467.2	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52400 ± 10 cm-1	Dingle 1975
15.1	1467.4	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52408 ± 10 (×1.242) cm-1	Kley 1973, Miescher 1974, est unc
3.8	1467.3	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52420 ± 12 (×2.044) cm-1	Miescher 1974, Huber 1979
2.3	1420.3	N2 (g) → N+ (g) + N (g)	Δ_rH°(0 K) = 24.2880 ± 0.0009 eV	Tang 2005
1.9	1706.3	(NH4)NO3 (cr,l) → N2 (g) + 1/2 O2 (g) + 2 H2O (cr,l)	Δ_rH°(293.65 K) = -49.44 ± 0.06 kcal/mol	Becker 1934
1.8	1420.1	N2 (g) → N+ (g) + N (g)	Δ_rH°(0 K) = 24.2888 ± 0.0010 eV	Tang 2005
1.8	1420.2	N2 (g) → N+ (g) + N (g)	Δ_rH°(0 K) = 24.2883 ± 0.0010 eV	Tang 2005
1.0	1470.4	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 626.47 ± 0.56 kJ/mol	Harding 2008
0.8	1469.10	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 149.82 ± 0.15 kcal/mol	Karton 2007a, Karton 2008
0.7	1397.11	N2 (g) → 2 N (g)	Δ_rH°(0 K) = 941.14 ± 0.15 kJ/mol	Thorpe 2021
0.7	1467.6	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 6.503 ± 0.004 (×1.719) eV	Brewer 1956, Frisch 1965
0.7	1468.10	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 149.78 ± 0.16 kcal/mol	Feller 2014
0.7	1933.4	HNO (g) → H (g) + N (g) + O (g)	Δ_rH°(0 K) = 823.10 ± 0.56 kJ/mol	Harding 2008
0.6	1470.2	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 626.74 ± 0.70 kJ/mol	Harding 2008
0.6	1940.4	HNO (g) → H (g) + NO (g)	Δ_rH°(0 K) = 16450 ± 10 cm-1	Dixon 1981, Dixon 1984, Dixon 1996
0.6	1482.1	1/2 N2 (g) + 1/2 O2 (g) → NO (g)	Δ_rH°(0 K) = 90.0 ± 0.8 kJ/mol	Szakacs 2011
0.6	1470.3	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 626.13 ± 0.74 kJ/mol	Harding 2008
0.5	1421.2	[N2]+ (g) → N+ (g) + N (g)	Δ_rH°(0 K) = 70248 ± 12 (×1.189) cm-1	Hertzler 1992, Douglas 1952, Hertzler 1990, Janin 1957, est unc
0.5	1470.1	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 626.22 ± 0.75 kJ/mol	Tajti 2004, est unc

Top 10 species with enthalpies of formation correlated to the Δ_fH° of NO (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
99.9	Nitrogen dioxide	ONO (g)	36.875	34.068	± 0.065	kJ/mol	46.00554 ± 0.00060	10102-44-0*0
99.8	Nitrosyl ion	[NO]+ (g)	984.504	984.499	± 0.065	kJ/mol	30.00559 ± 0.00031	14452-93-8*0
97.2	Dinitrogen tetraoxide	O2NNO2 (g)	20.18	10.90	± 0.14	kJ/mol	92.0111 ± 0.0012	10544-72-6*0
96.5	Nitrosyl chloride	ClNO (g)	54.470	52.569	± 0.067	kJ/mol	65.45884 ± 0.00095	2696-92-6*0
94.3	Dioxohydrazine	ONNO (g)	172.93	171.16	± 0.14	kJ/mol	60.01228 ± 0.00062	16824-89-8*0
94.3	Dioxohydrazine	ONNO (g, cis)	172.93	171.16	± 0.14	kJ/mol	60.01228 ± 0.00062	16824-89-8*2
89.9	Nitrogen sesquioxide	ONN(O)O (g)	90.76	86.19	± 0.15	kJ/mol	76.01168 ± 0.00091	10544-73-7*0
82.8	Nitrous acid	HONO (g)	-72.976	-78.633	± 0.078	kJ/mol	47.01348 ± 0.00061	7782-77-6*0
82.8	Nitrous acid	HONO (g, trans)	-72.976	-79.120	± 0.078	kJ/mol	47.01348 ± 0.00061	7782-77-6*1
82.4	Nitric oxide	NO (aq, undissoc)		79.227	± 0.079	kJ/mol	30.00614 ± 0.00031	10102-43-9*1000

Most Influential reactions involving NO (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
0.898	1628.3	ONNO (g, cis) → 2 NO (g)	Δ_rH°(0 K) = 697 ± 4 cm-1	Wade 2002, note NO, Gero 1948, Brown 1972, Huber 1979
0.799	1559.10	ONN(O)O (g) → NO (g) + ONO (g)	Δ_rG°(300 K) = -1.84 ± 0.07 kJ/mol	Beattie 1957, 3rd Law, apud Gurvich TPIS
0.782	1483.1	NO (g) → NO (aq, undissoc)	Δ_rG°(298.15 K) = 15.527 ± 0.05 kJ/mol	Young 1981a
0.746	2123.6	2 ClNO (g) → 2 NO (g) + Cl2 (g)	Δ_rH°(0 K) = 72.31 ± 0.04 kJ/mol	Beeson 1939, 3rd Law, apud Gurvich TPIS
0.723	1492.7	ONO (g) → NO (g) + O (g)	Δ_rH°(0 K) = 25128.56 ± 0.03 cm-1	Michalski 2004
0.710	1980.8	NO (g) + ONO (g) + H2O (g) → 2 HONO (g)	Δ_rG°(298.15 K) = -1.44 ± 0.10 kJ/mol	Vosper 1976, 3rd Law
0.598	1940.4	HNO (g) → H (g) + NO (g)	Δ_rH°(0 K) = 16450 ± 10 cm-1	Dixon 1981, Dixon 1984, Dixon 1996
0.584	1471.2	NO (g) → [NO]+ (g)	Δ_rH°(0 K) = 74721.7 ± 0.4 cm-1	Reiser 1988
0.380	1473.14	[NO]- (g) → NO (g)	Δ_rH°(0 K) = 0.029 ± 0.004 eV	Feller 2016, note unc2
0.374	1471.5	NO (g) → [NO]+ (g)	Δ_rH°(0 K) = 74721.5 ± 0.5 cm-1	Miescher 1976
0.349	7102.1	C6H5NO (g) → [C6H5]+ (g) + NO (g)	Δ_rH°(0 K) = 10.607 ± 0.020 eV	Stevens 2010a
0.341	1994.6	HOON (g, trans) → OH (g) + NO (g)	Δ_rH°(0 K) = 25.6 ± 4 kJ/mol	Talipov 2013, est unc
0.297	7103.1	C6H5NO (g) → C6H5 (g) + NO (g)	Δ_rG°(391 K) = 39.48 ± 0.5 kcal/mol	Park 1997, Yu 1994a, 3rd Law
0.263	1467.1	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52400 ± 10 cm-1	Callear 1970
0.263	1467.2	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52400 ± 10 cm-1	Dingle 1975
0.260	1492.6	ONO (g) → NO (g) + O (g)	Δ_rH°(0 K) = 25128.57 ± 0.05 cm-1	Jost 1996
0.243	1472.1	[NO]- (g) → NO (g)	Δ_rH°(0 K) = 0.026 ± 0.005 eV	Travers 1989
0.195	1483.3	NO (g) → NO (aq, undissoc)	Δ_rG°(298.15 K) = 15.48 ± 0.10 kJ/mol	Zacharia 2005
0.183	8215.5	[SiF3]+ (g) + NO (g) → SiF3 (g) + [NO]+ (g)	Δ_rH°(0 K) = 0.138 ± 0.040 eV	Ruscic W1RO
0.170	1467.4	NO (g) → N (g) + O (g)	Δ_rH°(0 K) = 52408 ± 10 (×1.242) cm-1	Kley 1973, Miescher 1974, est unc

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. 1.148 of the Thermochemical Network (2023); available at ATcT.anl.gov
4		T. L. Nguyen, J. Peeters, J.-F. Müller, A. Perera, D. H. Bross, B. Ruscic, and J. F. Stanton, Methanediol from Cloud-Processed Formaldehyde is Only a Minor Source of Atmospheric Formic Acid Natl. Acad. Sci. 120, e2304650120/1-8 (2023) [DOI: 10.1073/pnas.2304650120]
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.