Selected ATcT [1, 2] enthalpy of formation based on version 1.122r of the Thermochemical Network [3]

This version of ATcT results was generated from an expansion of version 1.122q [4, 5] to include a non-rigid rotor anharmonic oscillator (NRRAO) partition function for hydroxymethyl [6], as well as data on 42 additional species, some of which are related to soot formation mechanisms.

Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass		 ATcT ID
ChlorideCl- (aq)[Cl-]-166.992± 0.023kJ/mol35.45325 ±
0.00090		16887-00-6*800

Top contributors to the provenance of ΔfH° of Cl- (aq)

The 9 contributors listed below account for 94.2% of the provenance of ΔfH° of Cl- (aq).

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
24.7693.1 HCl (g) → HCl (aq) ΔrH°(298.15 K) = -17.884 ± 0.010 kcal/molGunn 1963, Gunn 1964, as quoted by CODATA Key Vals, Vanderzee 1963
17.3693.4 HCl (g) → HCl (aq) ΔrG°(298.15 K) = -36.009 ± 0.050 kJ/molAston 1955, as quoted by CODATA Key Vals
17.3693.5 HCl (g) → HCl (aq) ΔrG°(298.15 K) = -36.015 ± 0.050 kJ/molBates 1919, as quoted by CODATA Key Vals
16.3695.1 HCl (g) → HCl (aq, 2439 H2O) ΔrH°(298.15 K) = -17.810 ± 0.012 kcal/molVanderzee 1963
6.7693.3 HCl (g) → HCl (aq) ΔrG°(298.15 K) = -35.960 ± 0.080 kJ/molHaase 1963, as quoted by CODATA Key Vals
6.4691.1 1/2 H2 (g) + 1/2 Cl2 (g) → HCl (aq) ΔrG°(298.15 K) = -31.320 ± 0.020 (×1.044) kcal/molCerquetti 1968
2.4679.1 HCl (g) → H+ (g) + Cl- (g) ΔrH°(0 K) = 116289.0 ± 0.6 cm-1Martin 1998, note HCl
1.7691.2 1/2 H2 (g) + 1/2 Cl2 (g) → HCl (aq) ΔrH°(298.15 K) = -39.891 ± 0.040 kcal/molCerquetti 1968
1.1679.2 HCl (g) → H+ (g) + Cl- (g) ΔrH°(0 K) = 116287.7 ± 0.9 cm-1Hu 2003, note HCl

Top 10 species with enthalpies of formation correlated to the ΔfH° of Cl- (aq)

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
100.0 Hydrogen chlorideHCl (aq)Cl-166.992± 0.023kJ/mol36.46064 ±
0.00090		7647-01-0*800
94.3 Hydrogen chlorideHCl (aq, 2000 H2O)Cl-166.683± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*841
93.9 Hydrogen chlorideHCl (aq, 2439 H2O)Cl-166.713± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*951
93.8 Hydrogen chlorideHCl (aq, 1000 H2O)Cl-166.565± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*839
93.5 Hydrogen chlorideHCl (aq, 600 H2O)Cl-166.452± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*834
93.2 Hydrogen chlorideHCl (aq, 3000 H2O)Cl-166.741± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*842
93.2 Hydrogen chlorideHCl (aq, 200 H2O)Cl-166.105± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*830
92.4 Hydrogen chlorideHCl (aq, 150 H2O)Cl-165.979± 0.024kJ/mol36.46064 ±
0.00090		7647-01-0*829
90.4 Hydrogen chlorideHCl (aq, 100 H2O)Cl-165.757± 0.025kJ/mol36.46064 ±
0.00090		7647-01-0*828
88.7 Hydrogen chlorideHCl (aq, 1500 H2O)Cl-166.637± 0.025kJ/mol36.46064 ±
0.00090		7647-01-0*840

Most Influential reactions involving Cl- (aq)

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
1.000690.1 HCl (aq) → H+ (aq) + Cl- (aq) ΔrH°(298.15 K) = 0.000 ± 0.000 kcal/moltriv
0.9511459.5 (NH4)Cl (cr) → [NH4]+ (aq) + Cl- (aq) ΔrG°(298.15 K) = -7.092 ± 0.020 kJ/molCODATA Key Vals
0.036999.1 Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq) ΔrH°(298.15 K) = -91.29 ± 0.40 (×3.83) kJ/molJohnson 1963, as quoted by CODATA Key Vals
0.036999.2 Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq) ΔrH°(298.15 K) = -91.29 ± 0.80 (×1.915) kJ/molSunner 1964, as quoted by CODATA Key Vals
0.0281109.1 Cl2 (g) + 3 I- (aq) → 2 Cl- (aq) + [I3]- (aq) ΔrH°(298.15 K) = -51.5 ± 1.1 kcal/molWartenberg 1930, Wartenberg 1931, Parker 1965
0.0221459.4 (NH4)Cl (cr) → [NH4]+ (aq) + Cl- (aq) ΔrH°(298.15 K) = 3.533 ± 0.015 (×2.089) kcal/molParker 1965, as quoted by CODATA Key Vals
0.021999.3 Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq) ΔrH°(298.15 K) = -91.55 ± 2.00 kJ/molThomsen 1882, as quoted by CODATA Key Vals
0.0131459.1 (NH4)Cl (cr) → [NH4]+ (aq) + Cl- (aq) ΔrH°(298.15 K) = 3.542 ± 0.005 (×8.175) kcal/molVanderzee 1972a
0.0031459.3 (NH4)Cl (cr) → [NH4]+ (aq) + Cl- (aq) ΔrH°(298.15 K) = 14.98 ± 0.20 (×1.646) kJ/molMakarov 1967, as quoted by CODATA Key Vals
0.0031459.2 (NH4)Cl (cr) → [NH4]+ (aq) + Cl- (aq) ΔrH°(298.15 K) = 14.979 ± 0.080 (×4.177) kJ/molTsvetkov 1969, as quoted by CODATA Key Vals
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. 1.122r of the Thermochemical Network, Argonne National Laboratory, Lemont, Illinois 2021 [DOI: 10.17038/CSE/1822363]; available at ATcT.anl.gov
4   D. Feller, D. H. Bross, and B. Ruscic,
Enthalpy of Formation of C2H2O4 (Oxalic Acid) from High-Level Calculations and the Active Thermochemical Tables Approach.
J. Phys. Chem. A 123, 3481-3496 (2019) [DOI: 10.1021/acs.jpca.8b12329]
5   B. K. Welch, R. Dawes, D. H. Bross, and B. Ruscic,
An Automated Thermochemistry Protocol Based on Explicitly Correlated Coupled-Cluster Theory: The Methyl and Ethyl Peroxy Families.
J. Phys. Chem. A 123, 5673-5682 (2019) [DOI: 10.1021/acs.jpca.8b12329]
6   D. H. Bross, H.-G. Yu, L. B. Harding, and B. Ruscic,
Active Thermochemical Tables: The Partition Function of Hydroxymethyl (CH2OH) Revisited.
J. Phys. Chem. A 123, 4212-4231 (2019) [DOI: 10.1021/acs.jpca.9b02295]
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]
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 [7]).
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.