Selected ATcT [1, 2] enthalpy of formation based on version 1.130 of the Thermochemical Network [3]

This version of ATcT results[4] was generated by additional expansion of version 1.128 [5,6] to include with the calculations provided in reference [4].

Azido radical

Formula: NNN (g)
CAS RN: 12596-60-0
ATcT ID: 12596-60-0*0
SMILES: [N]N=[N]
InChI: InChI=1S/N3/c1-3-2
InChIKey: DUAJIKVIRGATIW-UHFFFAOYSA-N
Hills Formula: N3

2D Image:

[N]N=[N]
Aliases: NNN; Azido radical; Azide radical; Azido; Azidyl; Triatomic nitrogen; Nitrogen trimer; Trinitrogen
Relative Molecular Mass: 42.02022 ± 0.00021

   ΔfH°(0 K)   ΔfH°(298.15 K)UncertaintyUnits
452.24449.66± 0.60kJ/mol

3D Image of NNN (g)

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Top contributors to the provenance of ΔfH° of NNN (g)

The 20 contributors listed below account only for 69.3% of the provenance of ΔfH° of NNN (g).
A total of 57 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
21.62090.1 HNNN (g) → H (g) NNN (g) ΔrH°(0 K) = 30970 ± 50 cm-1Cook 1999
7.52103.1 [NNN]- (aq) [I3]- (aq) → 3 N2 (g) + 3 I- (aq) ΔrH°(298.15 K) = -158.78 ± 0.2 kcal/molGray 1956
6.02082.11 HNNN (g) → H (g) + 3 N (g) ΔrH°(0 K) = 318.06 ± 0.30 kcal/molKarton 2011
5.42090.2 HNNN (g) → H (g) NNN (g) ΔrH°(0 K) = 30920 ± 100 cm-1Yuan 2008
5.01341.1 I2 (cr,l) I- (aq) → [I3]- (aq) ΔrH°(298.15 K) = 1.338 ± 0.256 kcal/molWu 1963
2.51340.1 Br2 (cr,l) + 3 I- (aq) → [I3]- (aq) + 2 Br- (aq) ΔrH°(298.15 K) = -29.355 ± 0.364 kcal/molWu 1963
1.91421.11 NNN (g) → N2 (g) N (g) ΔrH°(0 K) = 4.00 ± 1.0 kcal/molDixon 2004
1.91416.9 NNN (g) → 3 N (g) ΔrH°(0 K) = 228.34 ± 1.0 kcal/molDixon 2004
1.82100.1 HNNN (g) → HNNN (aq, undissoc) ΔrH°(298.15 K) = -8.1 ± 0.1 kcal/molD'Orazio 1963, as quoted by NBS Tables
1.82100.2 HNNN (g) → HNNN (aq, undissoc) ΔrG°(298.15 K) = -1.5 ± 0.1 kcal/molD'Orazio 1963, as quoted by NBS Tables
1.71417.1 NNN (g) → [NNN]+ (g) ΔrH°(0 K) = 11.06 ± 0.01 eVDyke 1982, Tarroni 2004
1.72082.10 HNNN (g) → H (g) + 3 N (g) ΔrH°(0 K) = 317.83 ± 0.56 kcal/molKarton 2011
1.72089.1 HNNN (g) → 1/2 H2 (g) + 3/2 N2 (g) ΔrH°(285.6 K) = -70.3 ± 0.5 (×1.139) kcal/molGunther 1935, apud Gurvich TPIS, as quoted by NBS Tables
1.31422.4 NNN (g) CO (g) [O2]+ (g) → [CO2]+ (g) N2 (g) NO (g) ΔrH°(0 K) = -113.80 ± 1.2 kcal/molRuscic W1RO
1.31420.9 [NNN]- (g) → 3 N (g) ΔrH°(0 K) = 290.18 ± 1.0 kcal/molDixon 2004
1.11422.3 NNN (g) CO (g) [O2]+ (g) → [CO2]+ (g) N2 (g) NO (g) ΔrH°(0 K) = -114.08 ± 1.3 kcal/molRuscic CBS-n
1.11422.2 NNN (g) CO (g) [O2]+ (g) → [CO2]+ (g) N2 (g) NO (g) ΔrH°(0 K) = -112.64 ± 1.3 kcal/molRuscic G4
1.11418.3 [NNN]- (g) → NNN (g) ΔrH°(0 K) = 2.68 ± 0.01 eVContinetti 1991
1.01422.1 NNN (g) CO (g) [O2]+ (g) → [CO2]+ (g) N2 (g) NO (g) ΔrH°(0 K) = -114.81 ± 1.4 kcal/molRuscic G3X
0.91423.4 [NNN]- (g) CO (g) O2 (g) → CO2 (g) N2 (g) [NO]- (g) ΔrH°(0 K) = -92.54 ± 1.2 kcal/molRuscic W1RO

Top 10 species with enthalpies of formation correlated to the ΔfH° of NNN (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 Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass
ATcT ID
64.2 Hydrazoic acidHNNN (g)N=[N+]=[N-]297.88291.58± 0.49kJ/mol43.02816 ±
0.00022
7782-79-8*0
53.5 Azide[NNN]- (g)[N]N=[N-]193.52190.02± 0.91kJ/mol42.02077 ±
0.00021
14343-69-2*0
53.3 Hydrazoic acidHNNN (aq, undissoc)N=[N+]=[N-]257.60± 0.48kJ/mol43.02816 ±
0.00022
7782-79-8*1000
52.1 Trinitrogen cation[NNN]+ (g)[N]N=[N+]1519.411516.78± 0.89kJ/mol42.01967 ±
0.00021
12185-03-4*0
50.4 Azide[NNN]- (aq)[N]N=[N-]272.58± 0.48kJ/mol42.02077 ±
0.00021
14343-69-2*800
50.4 Hydrazoic acidHNNN (aq)N=[N+]=[N-]272.58± 0.48kJ/mol43.02816 ±
0.00022
7782-79-8*800
48.7 Hydrazoic acidHNNN (cr,l)N=[N+]=[N-]261.46± 0.65kJ/mol43.02816 ±
0.00022
7782-79-8*500
36.2 Hydrazoic acid cation[HNNN]+ (g)N=[N+]=[N]1333.631327.96± 0.83kJ/mol43.02761 ±
0.00022
58852-14-5*0
27.4 Triazirinylium ion[N(NN)]+ (g)[N]1N=[N+]11608.81605.9± 1.6kJ/mol42.01967 ±
0.00021
92220-05-8*0
-30.0 Triiodide[I3]- (aq)I[I-]I-51.32± 0.80kJ/mol380.713959 ±
0.000090
14900-04-0*800

Most Influential reactions involving NNN (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
0.6441418.3 [NNN]- (g) → NNN (g) ΔrH°(0 K) = 2.68 ± 0.01 eVContinetti 1991
0.6321417.1 NNN (g) → [NNN]+ (g) ΔrH°(0 K) = 11.06 ± 0.01 eVDyke 1982, Tarroni 2004
0.6052090.1 HNNN (g) → H (g) NNN (g) ΔrH°(0 K) = 30970 ± 50 cm-1Cook 1999
0.1512090.2 HNNN (g) → H (g) NNN (g) ΔrH°(0 K) = 30920 ± 100 cm-1Yuan 2008
0.1461432.6 NNN (g) → [N(NN)]+ (g) ΔrH°(0 K) = 11.958 ± 0.040 eVRuscic W1RO
0.1361431.7 N(NN) (g) → NNN (g) ΔrH°(0 K) = -31.47 ± 1.2 kcal/molRuscic W1RO
0.1151431.4 N(NN) (g) → NNN (g) ΔrH°(0 K) = -31.32 ± 1.3 kcal/molRuscic G4
0.0991431.3 N(NN) (g) → NNN (g) ΔrH°(0 K) = -32.30 ± 1.4 kcal/molRuscic G3X
0.0827903.6 NCNNN (g) → CN (g) NNN (g) ΔrH°(0 K) = 4.011 ± 0.065 eVRuscic W1RO
0.0761431.5 N(NN) (g) → NNN (g) ΔrH°(0 K) = -31.70 ± 1.6 kcal/molRuscic CBS-n
0.0727903.5 NCNNN (g) → CN (g) NNN (g) ΔrH°(0 K) = 3.992 ± 0.069 eVRuscic CBS-n
0.0727903.3 NCNNN (g) → CN (g) NNN (g) ΔrH°(0 K) = 4.015 ± 0.069 eVRuscic G4
0.0711418.4 [NNN]- (g) → NNN (g) ΔrH°(0 K) = 2.68 ± 0.03 eVYang 2004
0.0617903.2 NCNNN (g) → CN (g) NNN (g) ΔrH°(0 K) = 3.998 ± 0.075 eVRuscic G3X
0.0541444.5 NNNN (g, Cs) → NNN (g) N (g) ΔrH°(0 K) = 54.57 ± 1.50 kcal/molRuscic W1RO
0.0471444.4 NNNN (g, Cs) → NNN (g) N (g) ΔrH°(0 K) = 54.79 ± 1.60 kcal/molRuscic CBS-n
0.0471444.2 NNNN (g, Cs) → NNN (g) N (g) ΔrH°(0 K) = 54.66 ± 1.60 kcal/molRuscic G4
0.0441432.3 NNN (g) → [N(NN)]+ (g) ΔrH°(0 K) = 11.963 ± 0.073 eVRuscic G4
0.0411432.5 NNN (g) → [N(NN)]+ (g) ΔrH°(0 K) = 12.037 ± 0.075 eVRuscic CBS-n
0.0411444.1 NNNN (g, Cs) → NNN (g) N (g) ΔrH°(0 K) = 54.70 ± 1.72 kcal/molRuscic G3X


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 21st 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. 1.130 of the Thermochemical Network. Argonne National Laboratory, Lemont, Illinois 2023; available at ATcT.anl.gov
[DOI: 10.17038/CSE/1997229]
4   N. Genossar, P. B. Changala, B. Gans, J.-C. Loison, S. Hartweg, M.-A. Martin-Drumel, G. A. Garcia, J. F. Stanton, B. Ruscic, and J. H. Baraban
Ring-Opening Dynamics of the Cyclopropyl Radical and Cation: the Transition State Nature of the Cyclopropyl Cation
J. Am. Chem. Soc. 144, 18518-18525 (2022) [DOI: 10.1021/jacs.2c07740]
5   B. Ruscic and D. H. Bross
Active Thermochemical Tables: The Thermophysical and Thermochemical Properties of Methyl, CH3, and Methylene, CH2, Corrected for Nonrigid Rotor and Anharmonic Oscillator Effects.
Mol. Phys. e1969046 (2021) [DOI: 10.1080/00268976.2021.1969046]
6   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]
7   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]
8   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 [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.