Cyclopropanecarbonitrile

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Gas 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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Quantity Value Units Method Reference Comment
Δfgas43.7 ± 0.2kcal/molCcbFuchs, Hallman, et al., 1982Heat of combustion is not reported, see Hall and Baldt, 1971
Δfgas43.17kcal/molCcrHall and Baldt, 1971 

Phase change 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:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
ALS - Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein
AC - William E. Acree, Jr., James S. Chickos
DRB - Donald R. Burgess, Jr.

Quantity Value Units Method Reference Comment
Tboil408.2KN/AWeast and Grasselli, 1989BS
Tboil407. to 408.KN/AFrinton Laboratories Inc., 1986BS
Tboil408.2KN/AMajer and Svoboda, 1985 
Tboil404.9KN/AHammond and Todd, 1954Uncertainty assigned by TRC = 3. K; TRC
Quantity Value Units Method Reference Comment
Δvap9.8 ± 0.5kcal/molAVGN/AAverage of 6 values; Individual data points

Enthalpy of vaporization

ΔvapH (kcal/mol) Temperature (K) Method Reference Comment
8.497408.2N/AMajer and Svoboda, 1985 
9.42325.BGBaldt and Hall, 1971Based on data from 310. to 391. K.; AC

In addition to the Thermodynamics Research Center (TRC) data available from this site, much more physical and chemical property data is available from the following TRC products:


Gas phase ion energetics 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 evaluated as indicated in comments:
HL - Edward P. Hunter and Sharon G. Lias

Data compiled as indicated in comments:
B - John E. Bartmess
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

Quantity Value Units Method Reference Comment
Proton affinity (review)193.2kcal/molN/AHunter and Lias, 1998HL
Quantity Value Units Method Reference Comment
Gas basicity185.8kcal/molN/AHunter and Lias, 1998HL

Ionization energy determinations

IE (eV) Method Reference Comment
10.25PEWillett and Baer, 1980LLK
11.2 ± 0.2EIKiser and Hobrock, 1962RDSH

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
CH2N+11.50?PIWillett and Baer, 1980LLK
CN+19.5 ± 0.4?EIKiser and Hobrock, 1962RDSH
C2H3+12.65?PIWillett and Baer, 1980LLK
C2H3N+11.00C2H2EISakurai and Jennings, 1981LLK
C2H3N+11.00?PIWillett and Baer, 1980LLK
C3H2N+11.75?PIWillett and Baer, 1980LLK
C3H3+11.80?PIWillett and Baer, 1980LLK
C3H4+11.20?PIWillett and Baer, 1980LLK
C3H5+12.70 ± 0.15CNEIKiser and Hobrock, 1962RDSH
C4H4N+12.10HPIWillett and Baer, 1980LLK

De-protonation reactions

C4H4N- + Hydrogen cation = Cyclopropanecarbonitrile

By formula: C4H4N- + H+ = C4H5N

Quantity Value Units Method Reference Comment
Δr375.4 ± 2.2kcal/molG+TSBartmess, Scott, et al., 1979gas phase; Acid: cyanocyclopropane; value altered from reference due to change in acidity scale; B
Quantity Value Units Method Reference Comment
Δr367.8 ± 2.0kcal/molIMREBartmess, Scott, et al., 1979gas phase; Acid: cyanocyclopropane; value altered from reference due to change in acidity scale; B

References

Go To: Top, Gas phase thermochemistry data, Phase change data, Gas phase ion energetics data, Notes

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

Fuchs, Hallman, et al., 1982
Fuchs, R.; Hallman, J.H.; Perlman, M.O., Thermochemistry of conjugation of simple cyclopropane derivatives, Can. J. Chem., 1982, 60, 1832-1835. [all data]

Hall and Baldt, 1971
Hall, H.K., Jr.; Baldt, J.H., Thermochemistry of strained-ring bridgehead nitriles and esters, J. Am. Chem. Soc., 1971, 93, 140-145. [all data]

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Frinton Laboratories Inc., 1986
Frinton Laboratories Inc., Catalog Number 11, Frinton Laboratories Inc., Vineland, NJ, 1986, 99. [all data]

Majer and Svoboda, 1985
Majer, V.; Svoboda, V., Enthalpies of Vaporization of Organic Compounds: A Critical Review and Data Compilation, Blackwell Scientific Publications, Oxford, 1985, 300. [all data]

Hammond and Todd, 1954
Hammond, G.S.; Todd, R.W., The Low Reactivity of Cyclopropane Derivatives twoard Free Radicals, J. Am. Chem. Soc., 1954, 76, 4081. [all data]

Baldt and Hall, 1971
Baldt, J.H.; Hall, H.K.K., Jr., Thermochemistry of strained-ring bridgehead nitriles and esters, J. Am. Chem. Soc., 1971, 93, 140-145. [all data]

Hunter and Lias, 1998
Hunter, E.P.; Lias, S.G., Evaluated Gas Phase Basicities and Proton Affinities of Molecules: An Update, J. Phys. Chem. Ref. Data, 1998, 27, 3, 413-656, https://doi.org/10.1063/1.556018 . [all data]

Willett and Baer, 1980
Willett, G.D.; Baer, T., Thermochemistry and dissociation dynamics of state-selected C4H4X ions. 3. C4H5N+, J. Am. Chem. Soc., 1980, 102, 6774. [all data]

Kiser and Hobrock, 1962
Kiser, R.W.; Hobrock, B.G., The ionization potentials of cyclopropyl radical and cyclopropyl cyanide, J. Phys. Chem., 1962, 66, 957. [all data]

Sakurai and Jennings, 1981
Sakurai, H.; Jennings, K.R., A study of the structures of decomposing and non-decomposing [C4H5N]+ ions formed from different neutral species, Org. Mass Spectrom., 1981, 16, 393. [all data]

Bartmess, Scott, et al., 1979
Bartmess, J.E.; Scott, J.A.; McIver, R.T., Jr., The gas phase acidity scale from methanol to phenol, J. Am. Chem. Soc., 1979, 101, 6047. [all data]


Notes

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