Selected ATcT [1, 2] enthalpy of formation based on version 1.202 of the Thermochemical Network [3]

This version of ATcT results[3] was generated by additional expansion of version 1.176 in order to include species related to the thermochemistry of glycine[4].

Bromochlorane

Formula: BrCl (g)

CAS RN: 13863-41-7

ATcT ID: 13863-41-7*0

SMILES: ClBr

SMILES: BrCl

InChI: InChI=1S/BrCl/c1-2

InChIKey: CODNYICXDISAEA-UHFFFAOYSA-N

Hills Formula: Br1Cl1

2D Image:

Aliases: BrCl; Bromochlorane; Bromine chloride; Bromine monochloride; Bromochloride; Chlorine bromide; Chlorine monobromide; Monobromomonochloride; Monobromomonochlorine; Monochloromonobromide; Monochloromonobromine

Relative Molecular Mass: 115.3567 ± 0.0013

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
21.891	14.447	± 0.059	kJ/mol

3D Image of BrCl (g)

spin ON spin OFF

Top contributors to the provenance of Δ_fH° of BrCl (g)

The 2 contributors listed below account for 90.2% of the provenance of Δ_fH° of BrCl (g).

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
81.3	1108.2	Br2 (cr,l) → Br2 (g)	Δ_rH°(298.15 K) = 7.386 ± 0.027 kcal/mol	Hildenbrand 1958
8.8	1222.6	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(295.15 K) = 5.419 ± 0.049 kJ/mol	Tellinghuisen 2003, 3rd Law

Top 10 species with enthalpies of formation correlated to the Δ_fH° of BrCl (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
93.5	Dibromine	Br2 (g)	45.70	30.90	± 0.11	kJ/mol	159.8080 ± 0.0020	7726-95-6*0
93.5	Bromine atom	Br (g)	117.925	111.863	± 0.055	kJ/mol	79.90400 ± 0.00100	10097-32-2*0
93.5	Bromine atom	Br (g, 2P3/2)	117.925	111.863	± 0.055	kJ/mol	79.90400 ± 0.00100	10097-32-2*1
93.5	Bromine atom	Br (g, 2P1/2)	162.009	155.947	± 0.055	kJ/mol	79.90400 ± 0.00100	10097-32-2*2
93.5	Bromide	Br- (g)	-206.612	-212.674	± 0.055	kJ/mol	79.90455 ± 0.00100	24959-67-9*0
93.0	Bromanylium	Br+ (g)	1257.786	1251.723	± 0.056	kJ/mol	79.90345 ± 0.00100	22541-56-6*0
77.7	Iodine monobromide	IBr (g)	49.727	40.780	± 0.066	kJ/mol	206.8085 ± 0.0010	7789-33-5*0
45.4	Diatomic bromine cation	[Br2]+ (g)	1060.34	1045.39	± 0.23	kJ/mol	159.8075 ± 0.0020	12595-71-0*0
33.7	Hydrogen bromide	HBr (g)	-27.51	-35.36	± 0.12	kJ/mol	80.9119 ± 0.0010	10035-10-6*0
33.7	Bromoniumyl	[HBr]+ (g)	1098.16	1090.32	± 0.12	kJ/mol	80.9114 ± 0.0010	12258-64-9*0

Most Influential reactions involving BrCl (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
0.706	1222.6	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(295.15 K) = 5.419 ± 0.049 kJ/mol	Tellinghuisen 2003, 3rd Law
0.211	6384.1	CF3Br (g) + Cl2 (g) → CF3Cl (g) + BrCl (g)	Δ_rH°(298.15 K) = -10.69 ± 0.30 kcal/mol	Coomber 1967b, as quoted by Cox 1970
0.204	1269.1	HOBr (g) + Cl (g) → BrCl (g) + OH (g)	Δ_rG°(298.15 K) = -10.14 ± 1.04 kJ/mol	Loewenstein 1984, Kukui 1996, Monks 1993a, Loewenstein 1984
0.137	6408.1	Br2 (g) + CCl4 (g) → BrCl (g) + CCl3Br (g)	Δ_rH°(298.15 K) = 8.84 ± 0.30 kcal/mol	Mendenhall 1973, as quoted by Pedley 1986
0.118	1219.5	BrCl (g) → Br (g) + Cl (g)	Δ_rH°(0 K) = 18027 ± 5 cm-1	Tellinghuisen 2003a
0.117	1220.9	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(301.15 K) = 5.54 ± 0.12 kJ/mol	Vesper 1934, 3rd Law, est unc
0.109	6385.1	CF3Cl (g) + Br2 (g) → CF3Br (g) + BrCl (g)	Δ_rH°(298.15 K) = 10.49 ± 0.40 (×1.044) kcal/mol	Coomber 1967b, as quoted by Cox 1970
0.013	1219.2	BrCl (g) → Br (g) + Cl (g)	Δ_rH°(0 K) = 18023 ± 15 cm-1	Brown 1988
0.008	1220.4	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(298.15 K) = 5.45 ± 0.45 kJ/mol	Gray 1930, Vesper 1934, 3rd Law, est unc
0.008	1222.2	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(298.15 K) = 5.81 ± 0.45 kJ/mol	Bartlett 1999, 3rd Law
0.007	1222.5	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(298.15 K) = 5.73 ± 0.49 kJ/mol	Maric 1994, 3rd Law
0.004	1222.4	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(298.15 K) = 4.82 ± 0.10 (×6.304) kJ/mol	Cooper 1998, 3rd Law
0.004	1220.11	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(298.15 K) = 4.80 ± 0.45 (×1.445) kJ/mol	Brauer 1935, 3rd Law, est unc
0.003	1221.2	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(462 K) = 7.34 ± 0.70 kJ/mol	Beeson 1939a, 3rd Law, est unc
0.003	1221.8	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(310 K) = 4.89 ± 0.40 (×1.756) kJ/mol	Mattraw 1954, 3rd Law, est unc
0.001	1220.7	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rH°(298.15 K) = 1.31 ± 1.0 kJ/mol	Jost 1931, 2nd Law, est unc
0.001	1220.6	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(298.15 K) = 4.73 ± 1.0 kJ/mol	Jost 1931, 3rd Law, est unc
0.000	1221.6	2 BrCl (g) → Br2 (g) + Cl2 (g)	Δ_rG°(500 K) = 8.40 ± 1.7 kJ/mol	Schutza 1938, 3rd Law, est unc
0.000	1219.1	BrCl (g) → Br (g) + Cl (g)	Δ_rH°(0 K) = 17934 ± 26 (×3.668) cm-1	Clyne 1979, Clyne 1978, Clyne 1978a
0.000	1219.9	BrCl (g) → Br (g) + Cl (g)	Δ_rH°(0 K) = 51.62 ± 0.3 kcal/mol	Feller 2008

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. 1.202 of the Thermochemical Network (2024); available at ATcT.anl.gov
4		B. Ruscic and D. H. Bross Accurate and Reliable Thermochemistry by Data Analysis of Complex Thermochemical Networks using Active Thermochemical Tables: The Case of Glycine Thermochemistry Faraday Discuss. (in press) (2024) [DOI: 10.1039/D4FD00110A]
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.