Allene
- Formula: C3H4
- Molecular weight: 40.0639
- IUPAC Standard InChIKey: IYABWNGZIDDRAK-UHFFFAOYSA-N
- CAS Registry Number: 463-49-0
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Other names: Propadiene; 1,2-Propadiene; sym-Allylene; Dimethylenemethane; CH2=C=CH2; Propa-1,2-diene
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Gas phase ion energetics data
Go To: Top, References, Notes
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
L - Sharon G. Lias
Data compiled as indicated in comments:
B - John E. Bartmess
LL - Sharon G. Lias and Joel F. Liebman
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
View reactions leading to C3H4+ (ion structure unspecified)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
IE (evaluated) | 9.692 ± 0.004 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 775.3 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 745.8 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
9.688 ± 0.002 | PE | Yang, Wang, et al., 1990 | LL |
10.06 | PE | Kimura, Katsumata, et al., 1981 | LLK |
9.691 ± 0.004 | PI | Stockbauer, McCulloh, et al., 1979 | LLK |
9.696 ± 0.002 | TE | Parr, Jason, et al., 1978 | LLK |
9.62 ± 0.02 | PE | Bieri, Burger, et al., 1977 | LLK |
9.62 | EI | Lossing, 1972 | LLK |
10.017 ± 0.003 | S | Iverson and Russell, 1972 | LLK |
9.53 ± 0.03 | PI | Matthews and Warneck, 1969 | RDSH |
9.83 | PE | Dewar and Worley, 1969 | RDSH |
9.69 | PE | Baker and Turner, 1969 | RDSH |
9.62 ± 0.04 | PI | Parr and Elder, 1968 | RDSH |
10. | PE | Leng and Nyberg, 1977 | Vertical value; LLK |
10.2 ± 0.1 | PE | Bieri, Burger, et al., 1977 | Vertical value; LLK |
10.02 | PE | Thomas and Thompson, 1974 | Vertical value; LLK |
10.07 | PE | Brogli, Crandall, et al., 1973 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C3H+ | 16.9 ± 0.1 | H2+H | TE | Parr, Jason, et al., 1978 | LLK |
C3H+ | 18.56 ± 0.05 | H2+H | EI | Franklin and Mogenis, 1967 | RDSH |
C3H2+ | 13.5 ± 0.2 | H2 | TE | Parr, Jason, et al., 1978 | LLK |
C3H2+ | 14.34 ± 0.08 | H2 | EI | Franklin and Mogenis, 1967 | RDSH |
C3H3+ | 11.60 ± 0.01 | H | PI | Stockbauer and Rosenstock, 1978 | LLK |
C3H3+ | 11.48 ± 0.02 | ? | TE | Parr, Jason, et al., 1978 | LLK |
C3H3+ | 11.47 | H | EI | Lossing, 1972 | LLK |
C3H3+ | 11.48 | H | PI | Matthews and Warneck, 1969 | RDSH |
C3H3+ | 11.48 ± 0.02 | H | PI | Parr and Elder, 1968 | RDSH |
C3H22+ | 32.5 ± 0.2 | ? | EI | Franklin and Mogenis, 1967 | RDSH |
De-protonation reactions
C3H3- + =
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1590. ± 8.4 | kJ/mol | D-EA | Robinson, Polak, et al., 1995 | gas phase; Neutral acid: allene. Propyne would be 1.0 kcal/mol less acidic.; B |
ΔrH° | 1596. ± 13. | kJ/mol | G+TS | Robinson, Polak, et al., 1995 | gas phase; Relative to MeOH at 375.0; kinetic scheme factors in isomerization; B |
ΔrH° | 1592. ± 8.8 | kJ/mol | D-EA | Oakes and Ellison, 1983 | gas phase; Neutral acid: allene. Propyne would be 1.0 kcal/mol less acidic.; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1560. ± 13. | kJ/mol | IMRE | Robinson, Polak, et al., 1995 | gas phase; Relative to MeOH at 375.0; kinetic scheme factors in isomerization; B |
ΔrG° | 1556. ± 9.2 | kJ/mol | H-TS | Oakes and Ellison, 1983 | gas phase; Neutral acid: allene. Propyne would be 1.0 kcal/mol less acidic.; B |
References
Go To: Top, 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.
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]
Yang, Wang, et al., 1990
Yang, Z.Z.; Wang, L.S.; Lee, Y.T.; Shirley, D.A.; Huang, S.Y.; Lester, W.A., Jr.,
Molecular beam photoelectron spectroscopy of allene,
Chem. Phys. Lett., 1990, 171, 9. [all data]
Kimura, Katsumata, et al., 1981
Kimura, K.; Katsumata, S.; Achiba, Y.; Yamazaki, T.; Iwata, S.,
Ionization energies, Ab initio assignments, and valence electronic structure for 200 molecules
in Handbook of HeI Photoelectron Spectra of Fundamental Organic Compounds, Japan Scientific Soc. Press, Tokyo, 1981. [all data]
Stockbauer, McCulloh, et al., 1979
Stockbauer, R.; McCulloh, K.E.; Parr, A.C.,
The ionization potential of allene,
Int. J. Mass Spectrom. Ion Phys., 1979, 31, 187. [all data]
Parr, Jason, et al., 1978
Parr, A.C.; Jason, A.J.; Stockbauer, R.,
Photoionization and threshold photoelectron-photoion coincidence study of allene from onset to 20eV,
Int. J. Mass Spectrom. Ion Phys., 1978, 26, 23. [all data]
Bieri, Burger, et al., 1977
Bieri, G.; Burger, F.; Heilbronner, E.; Maier, J.P.,
Valence ionization enrgies of hydrocarbons,
Helv. Chim. Acta, 1977, 60, 2213. [all data]
Lossing, 1972
Lossing, F.P.,
Free radicals by mass spectrometry. XLV. Ionization potentials and heats of formation of C3H3, C3H5, and C4H7 radicals and ions,
Can. J. Chem., 1972, 50, 3973. [all data]
Iverson and Russell, 1972
Iverson, A.A.; Russell, B.R.,
A medium resolution study of allene in the vacuum ultraviolet. I. Spectra and a preliminary ionization potential,
Spectrochim. Acta Part A, 1972, 28, 447. [all data]
Matthews and Warneck, 1969
Matthews, C.S.; Warneck, P.,
Heats of formation of CHO+ and C3H3+ by photoionization,
J. Chem. Phys. 5, 1969, 1, 854. [all data]
Dewar and Worley, 1969
Dewar, M.J.S.; Worley, S.D.,
Photoelectron spectra of molecules. I. Ionization potentials of some organic molecules and their interpretation,
J. Chem. Phys., 1969, 50, 654. [all data]
Baker and Turner, 1969
Baker, C.; Turner, D.W.,
Photoelectron spectra of allene and keten; Jahn-Teller distortion in the ionisation of allene,
Chem. Commun., 1969, 480. [all data]
Parr and Elder, 1968
Parr, A.C.; Elder, F.A.,
Photoionization of 1,3butadiene, 1,2-butadiene, allene, and propyne,
J. Chem. Phys., 1968, 49, 2659. [all data]
Leng and Nyberg, 1977
Leng, F.J.; Nyberg, G.L.,
Angular-distribution He(I)/Ne(I) photoelectron spectra of allene,
J. Chem. Soc. Faraday Trans. 2, 1977, 73, 1719. [all data]
Thomas and Thompson, 1974
Thomas, R.K.; Thompson, H.,
The photoelectron spectra of allene, deuteroallenes and tetrafluoroallene,
Proc. R. Soc. London A:, 1974, 339, 29. [all data]
Brogli, Crandall, et al., 1973
Brogli, F.; Crandall, J.K.; Heilbronner, E.; Kloster-Jensen, E.; Sojka, S.A.,
The photoelectron spectra of methyl-substituted allenes and of tetramethyl-bisallenyl,
J. Electron Spectrosc. Relat. Phenom., 1973, 2, 455. [all data]
Franklin and Mogenis, 1967
Franklin, J.L.; Mogenis, A.,
An electron impact study of ions from several dienes,
J. Phys. Chem., 1967, 71, 2820. [all data]
Stockbauer and Rosenstock, 1978
Stockbauer, R.; Rosenstock, H.M.,
Kinetic shift in methane allene ion fragmentation,
Int. J. Mass Spectrom. Ion Phys., 1978, 27, 185. [all data]
Robinson, Polak, et al., 1995
Robinson, M.S.; Polak, M.L.; Bierbaum, V.M.; DePuy, C.H.; Lineberger, W.C.,
Experimental Studies of Allene, Methylacetylene, and the Propargyl Radical: Bond Dissociation Energies, Gas-Phase Acidities, and Ion-Molecule Chemistry,
J. Am. Chem. Soc., 1995, 117, 25, 6766, https://doi.org/10.1021/ja00130a017
. [all data]
Oakes and Ellison, 1983
Oakes, J.M.; Ellison, B.G.,
Photoelectron spectroscopy of the allenyl anion CH2=C=CH-,
J. Am. Chem. Soc., 1983, 105, 2969. [all data]
Notes
Go To: Top, Gas phase ion energetics data, References
- Symbols used in this document:
AE Appearance energy IE (evaluated) Recommended ionization energy ΔrG° Free energy of reaction at standard conditions ΔrH° Enthalpy of reaction at standard conditions - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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