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:

C1C=CC=CC=C1
Aliases: CH2(CHCHCHCHCHCH); Cycloheptatriene; 1,3,5-Cycloheptatriene; Tropylidene; Tropilidene; UN 2603; cyc-C7H8
Relative Molecular Mass: 92.1384 ± 0.0056

   ΔfH°(0 K)   ΔfH°(298.15 K)UncertaintyUnits
154.44145.65± 0.92kJ/mol

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

The 20 contributors listed below account only for 74.2% of the provenance of ΔfH° 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
32.77064.1 CH2(CHCHCHCHCHCH) (g) + 3 H2 (g) → CH2(CH2CH2CH2CH2CH2CH2) (g) ΔrH°(355.15 K) = -72.862 ± 0.300 kcal/molConn 1939
5.27062.1 CH2(CHCHCHCHCHCH) (cr,l) + 9 O2 (g) → 7 CO2 (g) + 4 H2O (cr,l) ΔrH°(297.0 K) = -965.46 ± 0.5 (×1.874) kcal/molJackson 1971
4.67063.1 CH2(CHCHCHCHCHCH) (cr,l) → CH2(CHCHCHCHCHCH) (g) ΔrH°(298.15 K) = 9.25 ± 0.05 kcal/molFinke 1956
3.67061.5 CH2(CHCHCHCHCHCH) (g) CH2CH2 (g) → CH2(CHCHCHCH) (g) CH2CHCHCH2 (g) ΔrH°(0 K) = 1.39 ± 0.9 kcal/molRuscic W1RO
3.47046.2 CH2(CH2CH2CH2CH2CH2CH2) (cr,l) + 21/2 O2 (g) → 7 CO2 (g) + 7 H2O (cr,l) ΔrH°(298.15 K) = -1099.09 ± 0.14 kcal/molKaarsemaker 1952, as quoted by Cox 1970
2.97061.4 CH2(CHCHCHCHCHCH) (g) CH2CH2 (g) → CH2(CHCHCHCH) (g) CH2CHCHCH2 (g) ΔrH°(0 K) = 2.38 ± 1.0 kcal/molRuscic CBS-n
2.97061.2 CH2(CHCHCHCHCHCH) (g) CH2CH2 (g) → CH2(CHCHCHCH) (g) CH2CHCHCH2 (g) ΔrH°(0 K) = 2.26 ± 1.0 kcal/molRuscic G4
2.47061.1 CH2(CHCHCHCHCHCH) (g) CH2CH2 (g) → CH2(CHCHCHCH) (g) CH2CHCHCH2 (g) ΔrH°(0 K) = 2.33 ± 1.1 kcal/molRuscic G3X
2.27076.7 CH2(CHCHCHCHCHCH) (g) → [CH(CHCHCHCHCHCH)]+ (g) H (g) ΔrH°(0 K) = 9.400 ± 0.040 eVRuscic W1RO
1.77061.3 CH2(CHCHCHCHCHCH) (g) CH2CH2 (g) → CH2(CHCHCHCH) (g) CH2CHCHCH2 (g) ΔrH°(0 K) = 2.36 ± 1.3 kcal/molRuscic CBS-n
1.67079.5 CH(CHCHCHCHCHCH) (g) CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = 8.59 ± 0.85 kcal/molRuscic W1RO
1.47079.2 CH(CHCHCHCHCHCH) (g) CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = 8.60 ± 0.90 kcal/molRuscic G4
1.47079.4 CH(CHCHCHCHCHCH) (g) CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = 8.87 ± 0.90 kcal/molRuscic CBS-n
1.47079.1 CH(CHCHCHCHCHCH) (g) CH2(CHCHCHCH) (g) → CH(CHCHCHCH) (g) CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = 8.57 ± 0.90 kcal/molRuscic G3X
1.13982.5 CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = -6.65 ± 1.2 kcal/molRuscic W1RO
1.07065.1 CH2(CHCHCHCHCHCH) (g) → [C6H5CH2]+ (g) H (g) ΔrH°(0 K) = 9.738 ± 0.082 eVTorma 2019
1.03982.2 CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = -6.74 ± 1.3 kcal/molRuscic G4
1.03982.4 CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = -7.22 ± 1.3 kcal/molRuscic CBS-n
0.83982.1 CH2CHCH(CHCHCHCH) (g, perp) → CH2(CHCHCHCHCHCH) (g) ΔrH°(0 K) = -6.82 ± 1.4 kcal/molRuscic G3X
0.87077.5 CH2(CHCHCHCHCHCH) (g) → CH(CHCHCHCHCHCH) (g) H (g) ΔrH°(0 K) = 72.75 ± 1.50 kcal/molRuscic W1RO

Top 10 species with enthalpies of formation correlated to the ΔfH° 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 Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass
ATcT ID
97.3 CycloheptatrieneCH2(CHCHCHCHCHCH) (g)C1C=CC=CC=C1207.79184.37± 0.90kJ/mol92.1384 ±
0.0056
544-25-2*0
31.9 TropylCH(CHCHCHCHCHCH) (g)[CH]1C=CC=CC=C1296.84279.41± 0.94kJ/mol91.1305 ±
0.0056
3551-27-7*0
29.4 CycloheptaneCH2(CH2CH2CH2CH2CH2CH2) (g)C1CCCCCC1-72.42-117.91± 0.52kJ/mol98.1861 ±
0.0057
291-64-5*0
29.2 Tropylium[CH(CHCHCHCHCHCH)]+ (g)[CH+]1C=CC=CC=C1899.19879.42± 0.99kJ/mol91.1299 ±
0.0056
26811-28-9*0
27.6 CycloheptaneCH2(CH2CH2CH2CH2CH2CH2) (cr,l)C1CCCCCC1-126.57-156.46± 0.50kJ/mol98.1861 ±
0.0057
291-64-5*500
25.4 CyclopentadieneCH2(CHCHCHCH) (g)C1C=CC=C1151.87134.75± 0.49kJ/mol66.1011 ±
0.0040
542-92-7*0
23.9 5-Ethenyl-1,3-cyclopentadieneCH2CHCH(CHCHCHCH) (g, perp)C=CC1C=CC=C1237.1215.4± 1.4kJ/mol92.1384 ±
0.0056
29647-85-6*1
23.9 5-Ethenyl-1,3-cyclopentadieneCH2CHCH(CHCHCHCH) (g)C=CC1C=CC=C1237.1216.3± 1.4kJ/mol92.1384 ±
0.0056
29647-85-6*0
20.0 1,3-CycloheptadieneCH2(CHCHCHCHCH2CH2) (g, c-c)C1CC=CC=CC1123.6594.54± 0.78kJ/mol94.1543 ±
0.0056
4054-38-0*1
19.2 CyclohepteneCH2(CHCHCH2CH2CH2CH2) (g)C1CCC=CCC128.55-8.68± 0.74kJ/mol96.1702 ±
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
0.9977063.1 CH2(CHCHCHCHCHCH) (cr,l) → CH2(CHCHCHCHCHCH) (g) ΔrH°(298.15 K) = 9.25 ± 0.05 kcal/molFinke 1956
0.0537062.1 CH2(CHCHCHCHCHCH) (cr,l) + 9 O2 (g) → 7 CO2 (g) + 4 H2O (cr,l) ΔrH°(297.0 K) = -965.46 ± 0.5 (×1.874) kcal/molJackson 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 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. 1.176 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.