1H-Pyrazole

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Condensed phase thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
DH - Eugene S. Domalski and Elizabeth D. Hearing

Quantity Value Units Method Reference Comment
Δfsolid  CcbZaheeruddin and Lodhi, 1991uncertain value: 26.859 kcal/mol; ALS
Δfsolid25.2 ± 0.2kcal/molCcbJimenez, Roux, et al., 1987see Jimenez, Roux, et al., 1986; ALS
Δfsolid27.7 ± 1.1kcal/molCcbBedford, Edmondson, et al., 1962Reanalyzed by Cox and Pilcher, 1970, Original value = 28.3 ± 1.1 kcal/mol; ALS
Quantity Value Units Method Reference Comment
Δcsolid  CcbZaheeruddin and Lodhi, 1991uncertain value: -445.650 kcal/mol; ALS
Δcsolid-444.0 ± 0.1kcal/molCcbJimenez, Roux, et al., 1987see Jimenez, Roux, et al., 1986; ALS
Δcsolid-446.5 ± 1.1kcal/molCcbBedford, Edmondson, et al., 1962Reanalyzed by Cox and Pilcher, 1970, Original value = -447.1 ± 1.1 kcal/mol; ALS
Δcsolid-444.2kcal/molCcbZimmerman and Geisenfelder, 1961ALS

Constant pressure heat capacity of solid

Cp,solid (cal/mol*K) Temperature (K) Reference Comment
19.4298.15Jimenez, Roux, et al., 1987Cp given as 1.19 J/g*K.; DH
21.0300.DeWit, Offringa, et al., 1983T = 300 to 450 K.; DH

Reaction thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
B - John E. Bartmess
RCD - Robert C. Dunbar

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

C3H3N2- + Hydrogen cation = 1H-Pyrazole

By formula: C3H3N2- + H+ = C3H4N2

Quantity Value Units Method Reference Comment
Δr353.6 ± 2.4kcal/molG+TSGianola, Ichino, et al., 2006gas phase; B
Δr353.6 ± 2.4kcal/molG+TSTaft, Anvia, et al., 1986gas phase; value altered from reference due to change in acidity scale; B
Quantity Value Units Method Reference Comment
Δr346.4 ± 2.3kcal/molN/AGianola, Ichino, et al., 2006gas phase; B
Δr346.4 ± 2.3kcal/molIMRETaft, Anvia, et al., 1986gas phase; value altered from reference due to change in acidity scale; B

Lithium ion (1+) + 1H-Pyrazole = (Lithium ion (1+) • 1H-Pyrazole)

By formula: Li+ + C3H4N2 = (Li+ • C3H4N2)

Quantity Value Units Method Reference Comment
Δr44.7 ± 4.0kcal/molCIDTHuang and Rodgers, 2002RCD

Sodium ion (1+) + 1H-Pyrazole = (Sodium ion (1+) • 1H-Pyrazole)

By formula: Na+ + C3H4N2 = (Na+ • C3H4N2)

Quantity Value Units Method Reference Comment
Δr30.6 ± 2.2kcal/molCIDTHuang and Rodgers, 2002RCD

Potassium ion (1+) + 1H-Pyrazole = (Potassium ion (1+) • 1H-Pyrazole)

By formula: K+ + C3H4N2 = (K+ • C3H4N2)

Quantity Value Units Method Reference Comment
Δr20.0 ± 0.8kcal/molCIDTHuang and Rodgers, 2002RCD

References

Go To: Top, Condensed phase thermochemistry data, Reaction thermochemistry data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Zaheeruddin and Lodhi, 1991
Zaheeruddin, M.; Lodhi, Z.H., Enthalpies of formation of some cyclic compounds, Phys. Chem. (Peshawar Pak.), 1991, 10, 111-118. [all data]

Jimenez, Roux, et al., 1987
Jimenez, P.; Roux, M.V.; Turrion, C., Thermochemical properties of N-heterocyclic compounds. I. Enthalpies of combustion, vapour pressures and enthalpies of sublimation, and enthalpies of formation of pyrazole, imidazole, indazole, and benzimidazole, J. Chem. Thermodyn., 1987, 19, 985-992. [all data]

Jimenez, Roux, et al., 1986
Jimenez, P.; Roux, M.V.; Turrion, C.; Gomis, F., Thermochemical properties of some N-heterocyclic compounds, J. Calorim. Anal. Therm. Thermodyn. Chim., 1986, 17, 469-470. [all data]

Bedford, Edmondson, et al., 1962
Bedford, A.F.; Edmondson, P.B.; Mortimer, C.T., Heats of formation and bond energies. Part VI. n-Butyliso-butyraldimine, n-butylisobutylamine, pyrazole, and imidazole, J. Chem. Soc., 1962, 2927-2931. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Zimmerman and Geisenfelder, 1961
Zimmerman, H.; Geisenfelder, H., Uber die Mesomerieenergie von Azolen, Z. Electrochem., 1961, 65, 368-371. [all data]

DeWit, Offringa, et al., 1983
DeWit, H.G.M.; Offringa, J.C.A.; De Kruif, C.G.; Van Miltenburg, J.C., Thermodynamic properties of molecular organic crystals containing nitrogen, oxygen and sulfur. III. Molar heat capacities measured by differential scanning calorimetry, Thermochim. Acta, 1983, 65, 43-51. [all data]

Gianola, Ichino, et al., 2006
Gianola, A.J.; Ichino, T.; Kato, S.; Bierbaum, V.M.; Lineberger, W.C., Thermochemical studies of pyrazolide, J. Phys. Chem. A, 2006, 110, 27, 8457-8466, https://doi.org/10.1021/jp057499+ . [all data]

Taft, Anvia, et al., 1986
Taft, R.W.; Anvia, F.; Taagepera, M.; Catalan, J.; Elgueroy, J., Electrostatic proximity effects in the relative basicities of pyrazole, imidazole, pyridazine, and pyrimidine, J. Am. Chem. Soc., 1986, 108, 3237. [all data]

Huang and Rodgers, 2002
Huang, H.; Rodgers, M.T., Sigma versus Pi interactions in alkali metal ion binding to azoles: Threshold collision-induced dissociation and ab initio theory studies, J. Phys. Chem. A, 2002, 106, 16, 4277, https://doi.org/10.1021/jp013630b . [all data]


Notes

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