Selected ATcT [1, 2] enthalpy of formation based on version 1.124 of the Thermochemical Network [3]

This version of ATcT results was generated by additional expansion of version 1.122x [4] to include additional information relevant to the study of thermophysical and thermochemical properties of CH2 and CH3 using nonrigid rotor anharmonic oscillator (NRRAO) partition functions [5], the development and benchmarking of a state-of-the-art computational approach that aims to reproduce total atomization energies of small molecules within 10–15 cm-1 [6], as well as the study of the reversible reaction C2H3 + H2 ⇌ C2H4 + H ⇌ C2H5 [7]

Sulfur trioxide

Formula: OS(O)O (l)
CAS RN: 7446-11-9
ATcT ID: 7446-11-9*590
SMILES: O=S(=O)=O
InChI: InChI=1S/O3S/c1-4(2)3
InChIKey: AKEJUJNQAAGONA-UHFFFAOYSA-N
Hills Formula: O3S1

2D Image:

O=S(=O)=O
Aliases: OS(O)O; Sulfur trioxide; Oxosulfane dioxide; Sulfuric anhydride; Trioxo-lambda6-sulfane; Nisso Sulfane; S(O)(O)O; SO3
Relative Molecular Mass: 80.0642 ± 0.0061

   ΔfH°(0 K)   ΔfH°(298.15 K)UncertaintyUnits
-440.84± 0.30kJ/mol

Top contributors to the provenance of ΔfH° of OS(O)O (l)

The 11 contributors listed below account for 91.3% of the provenance of ΔfH° of OS(O)O (l).

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
37.68133.1 OSO (g) + 1/2 O2 (g) → OS(O)O (l) ΔrH°(298.15 K) = -144.21 ± 0.40 kJ/molNBS Tables 1989
16.88136.1 OS(O)O (l) → OS(O)O (g) ΔrH°(298.15 K) = 45.32 ± 0.40 kJ/molNBS Tables 1989
7.08101.1 S (cr,l) O2 (g) → OSO (g) ΔrH°(298.15 K) = -296.847 ± 0.200 kJ/molEckman 1929, note SO2
5.08140.14 OSO (g) + 1/2 O2 (g) → OS(O)O (g) ΔrG°(925 K) = -11.77 ± 0.36 kJ/molKapustinskii 1936, Kapustinskii 1936a, Gurvich TPIS, 3rd Law
4.28134.1 OS(O)O (cr,l) → OS(O)O (g) ΔrH°(298.15 K) = 58.79 ± 0.40 kJ/molNBS Tables 1989
4.28136.2 OS(O)O (l) → OS(O)O (g) ΔrH°(298.15 K) = 45.5 ± 0.8 kJ/molKondratev 1985
4.28135.1 OS(O)O (cr,l) → OS(O)O (l) ΔrH°(298.15 K) = 13.47 ± 0.40 kJ/molNBS Tables 1989
3.88205.1 S (cr,l) + 3/2 O2 (g) H2O (cr,l) → OS(O)(OH)2 (aq, 115 H2O) ΔrH°(298.15 K) = -143.85 ± 0.06 kcal/molGood 1960, CODATA Key Vals
3.48140.10 OSO (g) + 1/2 O2 (g) → OS(O)O (g) ΔrG°(985 K) = -6.44 ± 0.36 (×1.215) kJ/molBodenstein 1905, Gurvich TPIS, 3rd Law
2.68140.12 OSO (g) + 1/2 O2 (g) → OS(O)O (g) ΔrG°(940 K) = -10.4 ± 0.5 kJ/molTaylor 1931, Gurvich TPIS, 3rd Law
2.08205.2 S (cr,l) + 3/2 O2 (g) H2O (cr,l) → OS(O)(OH)2 (aq, 115 H2O) ΔrH°(298.15 K) = -143.92 ± 0.07 (×1.164) kcal/molMansson 1963, CODATA Key Vals

Top 10 species with enthalpies of formation correlated to the ΔfH° of OS(O)O (l)

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
58.7 Sulfur trioxideOS(O)O (cr,l)O=S(=O)=O-454.29± 0.37kJ/mol80.0642 ±
0.0061
7446-11-9*500
57.8 Sulfur trioxideOS(O)O (g)O=S(=O)=O-389.74-395.49± 0.24kJ/mol80.0642 ±
0.0061
7446-11-9*0
42.1 Sulfur dioxideOSO (g)O=S=O-294.13-296.67± 0.13kJ/mol64.0648 ±
0.0060
7446-09-5*0
42.1 Sulfur monoxideSO (g)S=O6.026.07± 0.13kJ/mol48.0654 ±
0.0060
13827-32-2*0
41.5 Oxosulfur[SO]+ (g)[S+]=O999.33999.93± 0.13kJ/mol48.0649 ±
0.0060
767269-11-4*0
41.4 Sulfonyl cation[OSO]+ (g)O=[S+]=O897.07894.81± 0.13kJ/mol64.0643 ±
0.0060
12439-77-9*0
40.1 Sulfur dioxideOSO (aq, undissoc)O=S=O-322.82± 0.14kJ/mol64.0648 ±
0.0060
7446-09-5*1000
39.5 Sulfurous acidS(O)(OH)2 (aq, undissoc)O=S(O)O-608.62± 0.14kJ/mol82.0801 ±
0.0061
7782-99-2*1000
39.3 Sulfuric acidOS(O)(OH)2 (cr,l)OS(=O)(=O)O-811.81-813.80± 0.13kJ/mol98.0795 ±
0.0061
7664-93-9*500
38.4 SulfurS (g)[S]276.90279.14± 0.14kJ/mol32.0660 ±
0.0060
7704-34-9*0

Most Influential reactions involving OS(O)O (l)

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
0.5988135.1 OS(O)O (cr,l) → OS(O)O (l) ΔrH°(298.15 K) = 13.47 ± 0.40 kJ/molNBS Tables 1989
0.4588133.1 OSO (g) + 1/2 O2 (g) → OS(O)O (l) ΔrH°(298.15 K) = -144.21 ± 0.40 kJ/molNBS Tables 1989
0.3928136.1 OS(O)O (l) → OS(O)O (g) ΔrH°(298.15 K) = 45.32 ± 0.40 kJ/molNBS Tables 1989
0.0988136.2 OS(O)O (l) → OS(O)O (g) ΔrH°(298.15 K) = 45.5 ± 0.8 kJ/molKondratev 1985
0.0078136.3 OS(O)O (l) → OS(O)O (g) ΔrH°(298.15 K) = 43.137 ± 3. kJ/molWinTable 2003


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. 1.124 of the Thermochemical Network, Argonne National Laboratory, Lemont, Illinois 2022; available at ATcT.anl.gov
[DOI: 10.17038/CSE/1885923]
4   Y. Ren, L. Zhou, A. Mellouki, V. Daële, M. Idir, S. S. Brown, B. Ruscic, Robert S. Paton, M. R. McGillen, and A. R. Ravishankara,
Reactions of NO3 with Aromatic Aldehydes: Gas-Phase Kinetics and Insights into the Mechanism of the Reaction.
Atmos. Chem. Phys. 21, 13537-13551 (2021) [DOI: 10.5194/acp2021-228]
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   T. L. Nguyen, D. H. Bross, B. Ruscic, G. B. Ellison, and J. F. Stanton,
Mechanism, Thermochemistry, and Kinetics of the Reversible Reactions: C2H3 + H2 ⇌ C2H4 + H ⇌ C2H5.
Faraday Discuss. , (Advance Article) (2022) [DOI: 10.1039/D1FD00124H]
8   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]
9   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 [8,9]).
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.