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

This version of ATcT results was generated from an expansion of version 1.122o [4] to include an updated enthalpy of formation for Hydrazine. [5].

Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass		 ATcT ID
Chloromethane cation[CH3Cl]+ (g)C[Cl+]1014.651007.89± 0.19kJ/mol50.4867 ±
0.0012		12538-71-5*0

Representative Geometry of [CH3Cl]+ (g)

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Top contributors to the provenance of ΔfH° of [CH3Cl]+ (g)

The 20 contributors listed below account only for 58.0% of the provenance of ΔfH° of [CH3Cl]+ (g).
A total of 262 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
28.44414.1 CH3Br (g) → [CH3]+ (g) + Br (g) ΔrH°(0 K) = 12.834 ± 0.002 eVSong 2001
5.14398.1 CH3Cl (g) + 3/2 O2 (g) → CO2 (g) + H2O (cr,l) + HCl (aq, 600 H2O) ΔrH°(298.15 K) = -764.00 ± 0.50 (×1.61) kJ/molFletcher 1971
3.71888.1 2 H2 (g) + C (graphite) → CH4 (g) ΔrG°(1165 K) = 37.521 ± 0.068 kJ/molSmith 1946, note COf, 3rd Law
2.1994.1 Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq) ΔrH°(298.15 K) = -91.29 ± 0.40 (×2.134) kJ/molJohnson 1963, as quoted by CODATA Key Vals
2.1994.2 Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq) ΔrH°(298.15 K) = -91.29 ± 0.80 (×1.067) kJ/molSunner 1964, as quoted by CODATA Key Vals
2.04401.10 CH3Cl (g) + H (g) → CH4 (g) + Cl (g) ΔrH°(0 K) = -7296 ± 100 cm-1Czako 2012
1.61004.1 [HBr]+ (g) → H (g) + Br+ (g) ΔrH°(0 K) = 31394.5 ± 20 (×2.181) cm-1Haugh 1971, Norling 1935
1.64417.1 CH3Br (g) + H2 (g) → CH4 (g) + HBr (g) ΔrH°(523.15 K) = -18.062 ± 0.321 kcal/molFowell 1965
1.54395.1 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 91057.0 ± 2.0 cm-1Grutter 2011
1.34621.4 3 CH3Cl (g) → CHCl3 (g) + 2 CH4 (g) ΔrH°(0 K) = -2.13 ± 1.0 kcal/molRuscic G4
1.14394.4 CH3Cl (g) → C (g) + 3 H (g) + Cl (g) ΔrH°(0 K) = 371.34 ± 0.4 kcal/molFeller 2008
0.9972.1 1/2 H2 (g) + 1/2 Br2 (g) → HBr (g) ΔrH°(376.15 K) = -12.470 ± 0.170 kcal/molLacher 1956a, Lacher 1956
0.84621.6 3 CH3Cl (g) → CHCl3 (g) + 2 CH4 (g) ΔrH°(0 K) = -0.33 ± 0.9 (×1.384) kcal/molRuscic W1RO
0.84621.5 3 CH3Cl (g) → CHCl3 (g) + 2 CH4 (g) ΔrH°(0 K) = -2.52 ± 1.3 kcal/molRuscic CBS-n
0.74621.3 3 CH3Cl (g) → CHCl3 (g) + 2 CH4 (g) ΔrH°(0 K) = -2.89 ± 1.1 (×1.215) kcal/molRuscic G3X
0.74431.2 4 CH3Br (g) + CCl4 (g) → 4 CH3Cl (g) + CBr4 (g) ΔrH°(0 K) = 3.39 ± 1.0 kcal/molRuscic G4
0.74433.1 2 CH3Br (l) + H2 (g) → 2 CH4 (g) + Br2 (cr,l) ΔrH°(298.15 K) = -6.60 ± 0.60 kcal/molAdams 1966, as quoted by Cox 1970
0.6966.6 HBr (g) + Cl (g) → HCl (g) + Br (g) ΔrH°(0 K) = -15.68 ± 0.2 kcal/molFeller 2008
0.6965.12 HBr (g) → H (g) + Br (g) ΔrH°(0 K) = 86.47 ± 0.2 kcal/molFeller 2008
0.61090.1 HI (g) + Br (g) → HBr (g) + I (g) ΔrH°(0 K) = -16.14 ± 0.2 kcal/molFeller 2008

Top 10 species with enthalpies of formation correlated to the ΔfH° of [CH3Cl]+ (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
99.2 ChloromethaneCH3Cl (g)CCl-74.63-82.56± 0.19kJ/mol50.4872 ±
0.0012		74-87-3*0
97.7 ChloromethaneCH3Cl (l)CCl-106.42-102.45± 0.19kJ/mol50.4872 ±
0.0012		74-87-3*590
69.3 BromomethaneCH3Br (g)CBr-20.86-36.26± 0.18kJ/mol94.9385 ±
0.0013		74-83-9*0
66.9 Methyl bromide cation[CH3Br]+ (g)C[Br+]996.25981.34± 0.18kJ/mol94.9380 ±
0.0013		12538-70-4*0
65.2 BromomethaneCH3Br (l)CBr-56.58-59.60± 0.19kJ/mol94.9385 ±
0.0013		74-83-9*590
-43.8 Hydrogen bromideHBr (aq, 3000 H2O)Br-120.69± 0.15kJ/mol80.9119 ±
0.0010		10035-10-6*842
-43.8 Hydrogen bromideHBr (aq, 2000 H2O)Br-120.64± 0.15kJ/mol80.9119 ±
0.0010		10035-10-6*841
-43.9 Hydrogen bromideHBr (aq, 2570 H2O)Br-120.67± 0.15kJ/mol80.9119 ±
0.0010		10035-10-6*952
-46.7 Bromoniumyl[HBr]+ (g)[BrH+]1097.731089.89± 0.14kJ/mol80.9114 ±
0.0010		12258-64-9*0
-46.7 Hydrogen bromideHBr (g)Br-27.94-35.79± 0.14kJ/mol80.9119 ±
0.0010		10035-10-6*0

Most Influential reactions involving [CH3Cl]+ (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
0.9864395.1 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 91057.0 ± 2.0 cm-1Grutter 2011
0.0064395.2 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.289 ± 0.003 eVKarlsson 1977
0.0024395.3 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.290 ± 0.005 eVLocht 2001a, est unc, Locht 2001
0.0004396.4 [CH3Cl]+ (g) → C (g) + 3 H (g) + Cl (g) ΔrH°(0 K) = 111.90 ± 1.50 kcal/molRuscic W1RO
0.0004396.2 [CH3Cl]+ (g) → C (g) + 3 H (g) + Cl (g) ΔrH°(0 K) = 112.02 ± 1.60 kcal/molRuscic G4
0.0004396.1 [CH3Cl]+ (g) → C (g) + 3 H (g) + Cl (g) ΔrH°(0 K) = 111.80 ± 1.72 kcal/molRuscic G3X
0.0004395.6 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.01 eVWerner 1974
0.0004395.7 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.01 eVWatanabe 1962
0.0004395.13 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.01 eVWatanabe 1957
0.0004395.8 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.01 eVDibeler 1965, est unc
0.0004395.5 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.01 eVLocht 2001, est unc
0.0004395.4 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.296 ± 0.010 eVLocht 2001, est unc
0.0004395.11 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.29 ± 0.02 eVFrost 1970
0.0004395.9 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.02 eVTurner 1970, est unc
0.0004395.10 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.29 ± 0.02 eVRagle 1970, est unc
0.0004395.12 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.28 ± 0.02 eVPotts 1970, est unc
0.0004395.14 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 11.26 ± 0.02 (×1.509) eVDewar 1969a, est unc
0.0004395.15 CH3Cl (g) → [CH3Cl]+ (g) ΔrH°(0 K) = 90500 ± 500 (×1.114) cm-1Price 1936, 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 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. 1.122p of the Thermochemical Network (2020); available at ATcT.anl.gov
4   P. B. Changala, T. L. Nguyen, J. H. Baraban, G. B. Ellison, J. F. Stanton, D. H. Bross, and B. Ruscic,
Active Thermochemical Tables: The Adiabatic Ionization Energy of Hydrogen Peroxide.
J. Phys. Chem. A 121, 8799-8806 (2017) [DOI: 10.1021/acs.jpca.7b06221] (highlighted on the journal cover)
5   D. Feller, D. H. Bross, and B. Ruscic,
Enthalpy of Formation of N2H4 (Hydrazine) Revisited.
J. Phys. Chem. A 121, 6187-6198 (2017) [DOI: 10.1021/acs.jpca.7b06017]
6   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 [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.