Selected ATcT [1, 2] enthalpy of formation based on version 1.176 of the Thermochemical Network [3]

This version of ATcT results[3] was generated by additional expansion of version 1.172 to include species related to Criegee intermediates that are involved in several ongoing studies[4].

Cycloheptatriene

Formula: CH2(CHCHCHCHCHCH) (cr,l)

CAS RN: 544-25-2

ATcT ID: 544-25-2*500

SMILES: C1C=CC=CC=C1

InChI: InChI=1S/C7H8/c1-2-4-6-7-5-3-1/h1-6H,7H2

InChIKey: CHVJITGCYZJHLR-UHFFFAOYSA-N

Hills Formula: C7H8

2D Image:

Aliases: CH2(CHCHCHCHCHCH); Cycloheptatriene; 1,3,5-Cycloheptatriene; Tropylidene; Tropilidene; UN 2603; cyc-C7H8

Relative Molecular Mass: 92.1384 ± 0.0056

Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units
154.44	145.65	± 0.92	kJ/mol

Top contributors to the provenance of Δ_fH° of CH2(CHCHCHCHCHCH) (cr,l)

The 20 contributors listed below account only for 74.2% of the provenance of Δ_fH° of CH2(CHCHCHCHCHCH) (cr,l).
A total of 60 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
32.7	7064.1	CH2(CHCHCHCHCHCH) (g) + 3 H2 (g) → CH2(CH2CH2CH2CH2CH2CH2) (g)	Δ_rH°(355.15 K) = -72.862 ± 0.300 kcal/mol	Conn 1939
5.2	7062.1	CH2(CHCHCHCHCHCH) (cr,l) + 9 O2 (g) → 7 CO2 (g) + 4 H2O (cr,l)	Δ_rH°(297.0 K) = -965.46 ± 0.5 (×1.874) kcal/mol	Jackson 1971
4.6	7063.1	CH2(CHCHCHCHCHCH) (cr,l) → CH2(CHCHCHCHCHCH) (g)	Δ_rH°(298.15 K) = 9.25 ± 0.05 kcal/mol	Finke 1956
3.6	7061.5	CH2(CHCHCHCHCHCH) (g) + CH2CH2 (g) → CH2(CHCHCHCH) (g) + CH2CHCHCH2 (g)	Δ_rH°(0 K) = 1.39 ± 0.9 kcal/mol	Ruscic W1RO
3.4	7046.2	CH2(CH2CH2CH2CH2CH2CH2) (cr,l) + 21/2 O2 (g) → 7 CO2 (g) + 7 H2O (cr,l)	Δ_rH°(298.15 K) = -1099.09 ± 0.14 kcal/mol	Kaarsemaker 1952, as quoted by Cox 1970
2.9	7061.4	CH2(CHCHCHCHCHCH) (g) + CH2CH2 (g) → CH2(CHCHCHCH) (g) + CH2CHCHCH2 (g)	Δ_rH°(0 K) = 2.38 ± 1.0 kcal/mol	Ruscic CBS-n
2.9	7061.2	CH2(CHCHCHCHCHCH) (g) + CH2CH2 (g) → CH2(CHCHCHCH) (g) + CH2CHCHCH2 (g)	Δ_rH°(0 K) = 2.26 ± 1.0 kcal/mol	Ruscic G4
2.4	7061.1	CH2(CHCHCHCHCHCH) (g) + CH2CH2 (g) → CH2(CHCHCHCH) (g) + CH2CHCHCH2 (g)	Δ_rH°(0 K) = 2.33 ± 1.1 kcal/mol	Ruscic G3X
2.2	7076.7	CH2(CHCHCHCHCHCH) (g) → [CH(CHCHCHCHCHCH)]+ (g) + H (g)	Δ_rH°(0 K) = 9.400 ± 0.040 eV	Ruscic W1RO
1.7	7061.3	CH2(CHCHCHCHCHCH) (g) + CH2CH2 (g) → CH2(CHCHCHCH) (g) + CH2CHCHCH2 (g)	Δ_rH°(0 K) = 2.36 ± 1.3 kcal/mol	Ruscic CBS-n
1.6	7079.5	CH(CHCHCHCHCHCH) (g) + CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) + CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = 8.59 ± 0.85 kcal/mol	Ruscic W1RO
1.4	7079.2	CH(CHCHCHCHCHCH) (g) + CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) + CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = 8.60 ± 0.90 kcal/mol	Ruscic G4
1.4	7079.4	CH(CHCHCHCHCHCH) (g) + CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) + CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = 8.87 ± 0.90 kcal/mol	Ruscic CBS-n
1.4	7079.1	CH(CHCHCHCHCHCH) (g) + CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) + CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = 8.57 ± 0.90 kcal/mol	Ruscic G3X
1.1	3982.5	CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = -6.65 ± 1.2 kcal/mol	Ruscic W1RO
1.0	7065.1	CH2(CHCHCHCHCHCH) (g) → [C6H5CH2]+ (g) + H (g)	Δ_rH°(0 K) = 9.738 ± 0.082 eV	Torma 2019
1.0	3982.2	CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = -6.74 ± 1.3 kcal/mol	Ruscic G4
1.0	3982.4	CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = -7.22 ± 1.3 kcal/mol	Ruscic CBS-n
0.8	3982.1	CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g)	Δ_rH°(0 K) = -6.82 ± 1.4 kcal/mol	Ruscic G3X
0.8	7077.5	CH2(CHCHCHCHCHCH) (g) → CH(CHCHCHCHCHCH) (g) + H (g)	Δ_rH°(0 K) = 72.75 ± 1.50 kcal/mol	Ruscic W1RO

Top 10 species with enthalpies of formation correlated to the Δ_fH° of CH2(CHCHCHCHCHCH) (cr,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	Δ_fH°(0 K)	Δ_fH°(298.15 K)	Uncertainty	Units	Relative Molecular Mass	ATcT ID
97.3	Cycloheptatriene	CH2(CHCHCHCHCHCH) (g)	207.79	184.37	± 0.90	kJ/mol	92.1384 ± 0.0056	544-25-2*0
31.9	Tropyl	CH(CHCHCHCHCHCH) (g)	296.84	279.41	± 0.94	kJ/mol	91.1305 ± 0.0056	3551-27-7*0
29.4	Cycloheptane	CH2(CH2CH2CH2CH2CH2CH2) (g)	-72.42	-117.91	± 0.52	kJ/mol	98.1861 ± 0.0057	291-64-5*0
29.2	Tropylium	[CH(CHCHCHCHCHCH)]+ (g)	899.19	879.42	± 0.99	kJ/mol	91.1299 ± 0.0056	26811-28-9*0
27.6	Cycloheptane	CH2(CH2CH2CH2CH2CH2CH2) (cr,l)	-126.57	-156.46	± 0.50	kJ/mol	98.1861 ± 0.0057	291-64-5*500
25.4	Cyclopentadiene	CH2(CHCHCHCH) (g)	151.87	134.75	± 0.49	kJ/mol	66.1011 ± 0.0040	542-92-7*0
23.9	5-Ethenyl-1,3-cyclopentadiene	CH2CHCH(CHCHCHCH) (g, perp)	237.1	215.4	± 1.4	kJ/mol	92.1384 ± 0.0056	29647-85-6*1
23.9	5-Ethenyl-1,3-cyclopentadiene	CH2CHCH(CHCHCHCH) (g)	237.1	216.3	± 1.4	kJ/mol	92.1384 ± 0.0056	29647-85-6*0
20.0	1,3-Cycloheptadiene	CH2(CHCHCHCHCH2CH2) (g, c-c)	123.65	94.54	± 0.78	kJ/mol	94.1543 ± 0.0056	4054-38-0*1
19.2	Cycloheptene	CH2(CHCHCH2CH2CH2CH2) (g)	28.55	-8.68	± 0.74	kJ/mol	96.1702 ± 0.0057	628-92-2*0

Most Influential reactions involving CH2(CHCHCHCHCHCH) (cr,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
0.997	7063.1	CH2(CHCHCHCHCHCH) (cr,l) → CH2(CHCHCHCHCHCH) (g)	Δ_rH°(298.15 K) = 9.25 ± 0.05 kcal/mol	Finke 1956
0.053	7062.1	CH2(CHCHCHCHCHCH) (cr,l) + 9 O2 (g) → 7 CO2 (g) + 4 H2O (cr,l)	Δ_rH°(297.0 K) = -965.46 ± 0.5 (×1.874) kcal/mol	Jackson 1971

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. 1.176 of the Thermochemical Network (2024); available at ATcT.anl.gov
4		T. L. Nguyen et al, ongoing studies (2024)
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.