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]

Ammonium bromide

Formula: (NH4)Br (cr)

CAS RN: 12124-97-9

ATcT ID: 12124-97-9*510

SMILES: [NH4+].[Br-]

InChI: InChI=1S/BrH.H3N/h1H;1H3

InChIKey: SWLVFNYSXGMGBS-UHFFFAOYSA-N

Hills Formula: Br1H4N1

2D Image:

Aliases: (NH4)Br; Ammonium bromide; NH4Br; FR-1; FR-11

Relative Molecular Mass: 97.9425 ± 0.0010

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
-253.64	-270.22	± 0.15	kJ/mol

Top contributors to the provenance of Δ_fH° of (NH4)Br (cr)

The 20 contributors listed below account only for 62.1% of the provenance of Δ_fH° of (NH4)Br (cr).
A total of 153 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
6.9	1061.2	Br2 (cr,l) → Br2 (g)	Δ_rH°(298.15 K) = 7.386 ± 0.027 kcal/mol	Hildenbrand 1958
6.7	1152.1	Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq)	Δ_rH°(298.15 K) = -91.29 ± 0.40 (×2.327) kJ/mol	Johnson 1963, as quoted by CODATA Key Vals
6.7	1152.2	Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq)	Δ_rH°(298.15 K) = -91.29 ± 0.80 (×1.164) kJ/mol	Sunner 1964, as quoted by CODATA Key Vals
4.5	1091.1	HBr (g) → HBr (aq, 2570 H2O)	Δ_rH°(298.15 K) = -20.286 ± 0.012 kcal/mol	Vanderzee 1963
4.3	1663.1	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.448 ± 0.015 kcal/mol	Vanderzee 1972
4.2	1670.5	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -7.849 ± 0.040 kJ/mol	CODATA Key Vals
3.9	5520.1	CH3Br (g) → [CH3]+ (g) + Br (g)	Δ_rH°(0 K) = 12.834 ± 0.002 eV	Song 2001
3.7	8300.1	S(O)(OH)2 (aq, 2500 H2O) + Br2 (cr,l) + H2O (cr,l) → OS(O)(OH)2 (aq, 2500 H2O) + 2 HBr (aq, 1250 H2O)	Δ_rH°(298.15 K) = -55.47 ± 0.11 (×2.538) kcal/mol	Johnson 1963
3.5	1095.1	HBr (aq, 3000 H2O) → HBr (aq)	Δ_rH°(298.15 K) = -0.239 ± 0.040 kJ/mol	NBS Tables 1989, Parker 1965, NBS TN270
3.5	1162.1	[HBr]+ (g) → H (g) + Br+ (g)	Δ_rH°(0 K) = 31394.5 ± 20 (×1.957) cm-1	Haugh 1971, Norling 1935
2.2	1088.1	1/2 H2 (g) + 1/2 Br2 (cr,l) → HBr (aq)	Δ_rG°(298.15 K) = -102.81 ± 0.80 kJ/mol	Jones 1934, as quoted by CODATA Key Vals
1.5	1602.1	1/2 N2 (g) + 3/2 H2 (g) → NH3 (g)	Δ_rH°(298.15 K) = -10.885 ± 0.010 kcal/mol	Larson 1923, Vanderzee 1972
1.4	5513.6	4 CH3Cl (g) → CCl4 (g) + 3 CH4 (g)	Δ_rH°(0 K) = 2.52 ± 0.30 kcal/mol	Karton 2017
1.4	1152.3	Cl2 (g) + 2 Br- (aq) → Br2 (cr,l) + 2 Cl- (aq)	Δ_rH°(298.15 K) = -91.55 ± 2.00 kJ/mol	Thomsen 1882, as quoted by CODATA Key Vals
1.4	1086.1	1/2 H2 (g) + 1/2 Br2 (g) → HBr (g)	Δ_rH°(376.15 K) = -12.470 ± 0.170 (×1.044) kcal/mol	Lacher 1956a, Lacher 1956
1.3	1306.1	Br2 (cr,l) + 3 I- (aq) → [I3]- (aq) + 2 Br- (aq)	Δ_rH°(298.15 K) = -29.355 ± 0.364 kcal/mol	Wu 1963
1.1	1079.12	HBr (g) → H (g) + Br (g)	Δ_rH°(0 K) = 86.47 ± 0.2 kcal/mol	Feller 2008
1.1	1080.6	HBr (g) + Cl (g) → HCl (g) + Br (g)	Δ_rH°(0 K) = -15.68 ± 0.2 kcal/mol	Feller 2008
1.0	1250.1	HI (g) + Br (g) → HBr (g) + I (g)	Δ_rH°(0 K) = -16.14 ± 0.2 kcal/mol	Feller 2008
1.0	1663.2	NH3 (g) → NH3 (aq, undissoc)	Δ_rH°(298.15 K) = -8.456 ± 0.030 kcal/mol	Stavaley 1971, Vanderzee 1972, as quoted by CODATA Key Vals

Top 10 species with enthalpies of formation correlated to the Δ_fH° of (NH4)Br (cr)

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°(298.15 K)	Uncertainty	Units	Relative Molecular Mass	ATcT ID
89.9	Bromide	Br- (aq)	-120.88	± 0.14	kJ/mol	79.90455 ± 0.00100	24959-67-9*800
89.9	Hydrogen bromide	HBr (aq)	-120.88	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*800
86.1	Hydrogen bromide	HBr (aq, 3000 H2O)	-120.64	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*842
86.1	Hydrogen bromide	HBr (aq, 20000 H2O)	-120.78	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*852
86.1	Hydrogen bromide	HBr (aq, 10000 H2O)	-120.74	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*850
86.1	Hydrogen bromide	HBr (aq, 50 H2O)	-119.49	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*822
86.1	Hydrogen bromide	HBr (aq, 500 H2O)	-120.35	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*833
86.1	Hydrogen bromide	HBr (aq, 600 H2O)	-120.39	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*834
86.1	Hydrogen bromide	HBr (aq, 5000 H2O)	-120.69	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*844
86.1	Hydrogen bromide	HBr (aq, 7000 H2O)	-120.72	± 0.14	kJ/mol	80.9119 ± 0.0010	10035-10-6*846

Most Influential reactions involving (NH4)Br (cr)

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
0.786	1670.5	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -7.849 ± 0.040 kJ/mol	CODATA Key Vals
0.199	1670.3	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rG°(298.15 K) = -1.883 ± 0.019 kcal/mol	Shults 1966, Stephenson 1968, est unc
0.014	1661.4	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(298.15 K) = 45.08 ± 0.17 kcal/mol	Smits 1928, JANAF 3, 3rd Law
0.012	1661.2	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rG°(643.3 K) = 3.316 ± 0.035 (×5.076) kcal/mol	Smith 1914, 3rd Law
0.004	1670.2	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rH°(298.15 K) = 4.007 ± 0.015 (×8.175) kcal/mol	Stephenson 1968
0.004	1670.4	(NH4)Br (cr) → [NH4]+ (aq) + Br- (aq)	Δ_rH°(298.15 K) = 4.01 ± 0.10 (×1.242) kcal/mol	Parker 1965, as quoted by CODATA Key Vals
0.003	1661.3	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(298.15 K) = 45.50 ± 0.17 (×2.044) kcal/mol	Smits 1928, JANAF 3, 2nd Law
0.001	1661.7	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rG°(589.4 K) = 28.72 ± 2.13 kJ/mol	Johnson 1909, 3rd Law
0.000	1661.1	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(643.3 K) = 42.77 ± 0.78 kcal/mol	Smith 1914, 2nd Law
0.000	1661.8	(NH4)Br (cr) → NH3 (g) + HBr (g)	Δ_rH°(589.4 K) = 197.44 ± 7.16 (×2.43) kJ/mol	Johnson 1909, 2nd Law

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. 1.124 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.