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

This version of ATcT results was partially described in Ruscic et al. [4], and was also used for the initial development of high-accuracy ANLn composite electronic structure methods [5].

Species Name Formula Image    ΔfH°(0 K)    ΔfH°(298.15 K) Uncertainty Units Relative
Molecular
Mass		 ATcT ID
CyclopenteneCH2(CH2CHCHCH2) (g)C1CC=CC158.1233.85± 0.45kJ/mol68.1170 ±
0.0040		142-29-0*0

Representative Geometry of CH2(CH2CHCHCH2) (g)

spin ON           spin OFF
          

Top contributors to the provenance of ΔfH° of CH2(CH2CHCHCH2) (g)

The 20 contributors listed below account only for 89.8% of the provenance of ΔfH° of CH2(CH2CHCHCH2) (g).
A total of 21 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
20.52613.1 CH2(CH2CH2CH2CH2) (l) + 15/2 O2 (g) → 5 CO2 (g) + 5 H2O (l) ΔrH°(298.15 K) = -3290.85 ± 0.72 kJ/molJohnson 1946
20.12618.2 CH2(CH2CHCHCH2) (l) + 7 O2 (g) → 5 CO2 (g) + 4 H2O (l) ΔrH°(298.15 K) = -744.54 ± 0.14 kcal/molLabbauf 1961
11.42617.2 CH2(CH2CHCHCH2) (l) → CH2(CH2CHCHCH2) (g) ΔrH°(300.15 K) = 6.78 ± 0.1 kcal/molLister 1941, est unc
8.12618.1 CH2(CH2CHCHCH2) (l) + 7 O2 (g) → 5 CO2 (g) + 4 H2O (l) ΔrH°(298.15 K) = -744.45 ± 0.17 (×1.297) kcal/molProsen 1944, Labbauf 1961, Epstein 1949
7.62615.1 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(298.15 K) = -26.67 ± 0.06 kcal/molDolliver 1937
6.72613.3 CH2(CH2CH2CH2CH2) (l) + 15/2 O2 (g) → 5 CO2 (g) + 5 H2O (l) ΔrH°(298.15 K) = -786.61 ± 0.30 kcal/molSpitzer 1947
3.32617.1 CH2(CH2CHCHCH2) (l) → CH2(CH2CHCHCH2) (g) ΔrH°(298.15 K) = 6.71 ± 0.07 (×2.65) kcal/molWagman 1949, Forziati 1950, Epstein 1949
2.92613.4 CH2(CH2CH2CH2CH2) (l) + 15/2 O2 (g) → 5 CO2 (g) + 5 H2O (l) ΔrH°(298.15 K) = -786.84 ± 0.14 (×3.221) kcal/molKaarsemaker 1952, as quoted by Cox 1970
2.8117.2 1/2 O2 (g) + H2 (g) → H2O (cr,l) ΔrH°(298.15 K) = -285.8261 ± 0.040 kJ/molRossini 1939, Rossini 1931, Rossini 1931b, note H2Oa, Rossini 1930
0.71519.7 C (graphite) + O2 (g) → CO2 (g) ΔrH°(298.15 K) = -393.464 ± 0.024 kJ/molHawtin 1966, note CO2e
0.72635.5 CH2(CH2CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH3 (g) → CH2(CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH2CH3 (g) ΔrH°(0 K) = 5.53 ± 0.85 kcal/molRuscic W1RO
0.62635.4 CH2(CH2CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH3 (g) → CH2(CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH2CH3 (g) ΔrH°(0 K) = 5.76 ± 0.90 kcal/molRuscic CBS-n
0.62635.1 CH2(CH2CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH3 (g) → CH2(CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH2CH3 (g) ΔrH°(0 K) = 5.97 ± 0.90 kcal/molRuscic G3X
0.62635.2 CH2(CH2CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH3 (g) → CH2(CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH2CH3 (g) ΔrH°(0 K) = 5.96 ± 0.90 kcal/molRuscic G4
0.52635.3 CH2(CH2CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH3 (g) → CH2(CH2CH2CH2CH2) (g) + CH3CH2CH2CH2CH2CH3 (g) ΔrH°(0 K) = 5.82 ± 1.0 kcal/molRuscic CBS-n
0.42614.5 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1250.52 ± 1.50 kcal/molRuscic W1RO
0.32611.5 CH2(CH2CH2CH2CH2) (g) + H2 (g) → CH3CH2CH2CH2CH3 (g) ΔrH°(0 K) = -16.46 ± 1.2 kcal/molRuscic W1RO
0.31642.1 2 H2 (g) + C (graphite) → CH4 (g) ΔrG°(1165 K) = 37.521 ± 0.068 kJ/molSmith 1946, note COf, 3rd Law
0.32614.4 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1250.33 ± 1.60 kcal/molRuscic CBS-n
0.32614.2 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1248.22 ± 1.60 kcal/molRuscic G4

Top 10 species with enthalpies of formation correlated to the ΔfH° of CH2(CH2CHCHCH2) (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
86.0 CyclopentaneCH2(CH2CH2CH2CH2) (g)C1CCCC1-45.01-77.58± 0.44kJ/mol70.1329 ±
0.0041		287-92-3*0
85.5 CyclopentaneCH2(CH2CH2CH2CH2) (l)C1CCCC1-106.26± 0.44kJ/mol70.1329 ±
0.0041		287-92-3*590
71.5 CyclopenteneCH2(CH2CHCHCH2) (l)C1CC=CC15.01± 0.42kJ/mol68.1170 ±
0.0040		142-29-0*590
61.6 1,3-CyclopentadieneCH2(CHCHCHCH) (l)C1C=CC=C1108.76± 0.61kJ/mol66.1011 ±
0.0040		542-92-7*590
47.3 1,3-CyclopentadieneCH2(CHCHCHCH) (g)C1C=CC=C1149.88132.76± 0.76kJ/mol66.1011 ±
0.0040		542-92-7*0
25.6 WaterH2O (cr, l, eq.press.)O-286.302-285.830± 0.027kJ/mol18.01528 ±
0.00033		7732-18-5*499
25.6 WaterH2O (cr,l)O-286.300-285.828± 0.027kJ/mol18.01528 ±
0.00033		7732-18-5*500
25.6 WaterH2O (l, eq.press.)O-285.830± 0.027kJ/mol18.01528 ±
0.00033		7732-18-5*589
25.6 WaterH2O (l)O-285.828± 0.027kJ/mol18.01528 ±
0.00033		7732-18-5*590
25.6 Oxonium[H3O]+ (aq)[OH3+]-285.828± 0.027kJ/mol19.02267 ±
0.00037		13968-08-6*800

Most Influential reactions involving CH2(CH2CHCHCH2) (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
0.8492615.1 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(298.15 K) = -26.67 ± 0.06 kcal/molDolliver 1937
0.6052617.2 CH2(CH2CHCHCH2) (l) → CH2(CH2CHCHCH2) (g) ΔrH°(300.15 K) = 6.78 ± 0.1 kcal/molLister 1941, est unc
0.1752617.1 CH2(CH2CHCHCH2) (l) → CH2(CH2CHCHCH2) (g) ΔrH°(298.15 K) = 6.71 ± 0.07 (×2.65) kcal/molWagman 1949, Forziati 1950, Epstein 1949
0.0322615.2 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(298.15 K) = -26.94 ± 0.13 (×2.378) kcal/molAllinger 1982
0.0052614.5 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1250.52 ± 1.50 kcal/molRuscic W1RO
0.0052614.2 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1248.22 ± 1.60 kcal/molRuscic G4
0.0052614.4 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1250.33 ± 1.60 kcal/molRuscic CBS-n
0.0042616.5 CH2(CH2CHCHCH2) (g) + C2H6 (g) → CH2(CH2CH2CH2CH2) (g) + C2H4 (g) ΔrH°(0 K) = 6.27 ± 0.9 kcal/molRuscic W1RO
0.0042614.1 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1248.20 ± 1.72 kcal/molRuscic G3X
0.0032616.2 CH2(CH2CHCHCH2) (g) + C2H6 (g) → CH2(CH2CH2CH2CH2) (g) + C2H4 (g) ΔrH°(0 K) = 5.99 ± 1.0 kcal/molRuscic G4
0.0032616.4 CH2(CH2CHCHCH2) (g) + C2H6 (g) → CH2(CH2CH2CH2CH2) (g) + C2H4 (g) ΔrH°(0 K) = 6.10 ± 1.0 kcal/molRuscic CBS-n
0.0032616.1 CH2(CH2CHCHCH2) (g) + C2H6 (g) → CH2(CH2CH2CH2CH2) (g) + C2H4 (g) ΔrH°(0 K) = 5.95 ± 1.1 kcal/molRuscic G3X
0.0022616.3 CH2(CH2CHCHCH2) (g) + C2H6 (g) → CH2(CH2CH2CH2CH2) (g) + C2H4 (g) ΔrH°(0 K) = 6.09 ± 1.3 kcal/molRuscic CBS-n
0.0022615.7 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(0 K) = -25.00 ± 1.2 kcal/molRuscic W1RO
0.0022614.3 CH2(CH2CHCHCH2) (g) → 5 C (g) + 8 H (g) ΔrH°(0 K) = 1246.78 ± 2.16 (×1.189) kcal/molRuscic CBS-n
0.0012615.4 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(0 K) = -24.27 ± 1.3 kcal/molRuscic G4
0.0012615.6 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(0 K) = -25.60 ± 1.3 kcal/molRuscic CBS-n
0.0012615.3 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(0 K) = -24.35 ± 1.4 kcal/molRuscic G3X
0.0012615.5 CH2(CH2CHCHCH2) (g) + H2 (g) → CH2(CH2CH2CH2CH2) (g) ΔrH°(0 K) = -23.94 ± 1.6 kcal/molRuscic CBS-n
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. 1.122 of the Thermochemical Network (2016); available at ATcT.anl.gov
4   B. Ruscic,
Active Thermochemical Tables: Sequential Bond Dissociation Enthalpies of Methane, Ethane, and Methanol and the Related Thermochemistry.
J. Phys. Chem. A 119, 7810-7837 (2015) [DOI: 10.1021/acs.jpca.5b01346]
5   S. J. Klippenstein, L. B. Harding, and B. Ruscic,
Ab initio Computations and Active Thermochemical Tables Hand in Hand: Heats of Formation of Core Combustion Species.
J. Phys. Chem. A 121, 6580-6602 (2017) [DOI: 10.1021/acs.jpca.7b05945]
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.