Acetylacetone
- Formula: C5H8O2
- Molecular weight: 100.1158
- IUPAC Standard InChIKey: YRKCREAYFQTBPV-UHFFFAOYSA-N
- CAS Registry Number: 123-54-6
- 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: 2,4-Pentanedione; Acetoacetone; Diacetylmethane; Pentane-2,4-dione; 2-Propanone, acetyl-; 2,4-Dioxopentane; 2,4-Pentadione; CH3COCH2COCH3; Acetone, acetyl-; ACAC; Pentanedione; Pentanedione-2,4; Acetyl 2-propanone; UN 2310; 2,4-Pentandione; Pentan-2,4-dione; NSC 5575
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Gas phase thermochemistry data
Go To: Top, Condensed phase thermochemistry data, Gas phase ion energetics data, Ion clustering data, References, Notes
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 |
---|---|---|---|---|---|
ΔfH°gas | -384.4 ± 1.3 | kJ/mol | Ccb | Hacking and Pilcher, 1979 | Heat of enolization=-11.3±0.4 kJ/mol |
ΔfH°gas | -420.1 | kJ/mol | Ion | Conrath, Van de Sande, et al., 1974 | Mass spectrometery (enol) |
ΔfH°gas | -376.1 ± 2.0 | kJ/mol | Cm | Melia and Merrifield, 1969 | Thermochemical cycle |
Condensed phase thermochemistry data
Go To: Top, Gas phase thermochemistry data, Gas phase ion energetics data, Ion clustering data, References, Notes
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 |
---|---|---|---|---|---|
ΔfH°liquid | -427.6 ± 1.1 | kJ/mol | Ccb | Hacking and Pilcher, 1979 | Heat of enolization=-11.3±0.4 kJ/mol |
ΔfH°liquid | -447.3 ± 8.0 | kJ/mol | Ccb | Vilcu and Perisanu, 1979 | |
ΔfH°liquid | -414.1 ± 2.0 | kJ/mol | Cm | Melia and Merrifield, 1969 | Thermochemical cycle |
ΔfH°liquid | -528.94 | kJ/mol | Ccb | Guinchant, 1918 | Author hf288_condensed[kcal/mol]=-131.2 kcal/mol |
Quantity | Value | Units | Method | Reference | Comment |
ΔcH°liquid | -2685.4 ± 0.8 | kJ/mol | Ccb | Hacking and Pilcher, 1979 | Heat of enolization=-11.3±0.4 kJ/mol; Corresponding ΔfHºliquid = -425.5 kJ/mol (simple calculation by NIST; no Washburn corrections) |
ΔcH°liquid | -2667. ± 12. | kJ/mol | Ccb | Vilcu and Perisanu, 1979 | Corresponding ΔfHºliquid = -443.88 kJ/mol (simple calculation by NIST; no Washburn corrections) |
ΔcH°liquid | -2687.0 ± 1.5 | kJ/mol | Ccb | Nicholson, 1957 | Corresponding ΔfHºliquid = -423.92 kJ/mol (simple calculation by NIST; no Washburn corrections) |
ΔcH°liquid | -2581.9 | kJ/mol | Ccb | Guinchant, 1918 | Author hf288_condensed[kcal/mol]=-131.2 kcal/mol; Corresponding ΔfHºliquid = -528.98 kJ/mol (simple calculation by NIST; no Washburn corrections) |
Gas phase ion energetics data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Ion clustering data, 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
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
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 |
---|---|---|---|---|---|
IE (evaluated) | 8.85 ± 0.02 | eV | N/A | N/A | L |
Quantity | Value | Units | Method | Reference | Comment |
Proton affinity (review) | 873.5 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Quantity | Value | Units | Method | Reference | Comment |
Gas basicity | 836.8 | kJ/mol | N/A | Hunter and Lias, 1998 | HL |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
8.85 ± 0.05 | PE | Houk, Davis, et al., 1973 | LLK |
8.82 ± 0.02 | PI | Shigorin, Filyugina, et al., 1967 | RDSH |
8.87 ± 0.03 | PI | Watanabe, Nakayama, et al., 1962 | RDSH |
9.63 ± 0.01 | PE | Hush, Livett, et al., 1987 | Vertical value; LBLHLM |
9.15 | PE | Cauletti, Furlani, et al., 1980 | Vertical value; LLK |
9.00 | PE | Schweig, Vermeer, et al., 1974 | Vertical value; LLK |
9.18 ± 0.07 | PE | Evans, Hamnett, et al., 1972 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C4H5O2+ | 10.7 ± 0.1 | CH3 | EI | Reichert and Westmore, 1969 | RDSH |
C4H5O2+ | 10.24 | CH3 | PI | Shigorin, Filyugina, et al., 1967 | RDSH |
De-protonation reactions
C5H7O2- + =
By formula: C5H7O2- + H+ = C5H8O2
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 1438. ± 8.8 | kJ/mol | G+TS | Taft and Bordwell, 1988 | gas phase; at 330K: neutral enol/keto ratio should be 8:1 ( Strohmeier and Höhne, 1952); B |
ΔrH° | 1438. ± 9.6 | kJ/mol | G+TS | Cumming and Kebarle, 1978 | gas phase; At 500K: neutral enol/keto ratio is 1.7:1, Folkendt, Weiss-Lopez, et al., 1989. ΔH=-4.7 kcal/mol, enol favored. Carbonyls anti in anion, via calc: Irikura, 1999; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 1409. ± 8.4 | kJ/mol | IMRE | Taft and Bordwell, 1988 | gas phase; at 330K: neutral enol/keto ratio should be 8:1 ( Strohmeier and Höhne, 1952); B |
ΔrG° | 1408. ± 8.4 | kJ/mol | IMRE | Cumming and Kebarle, 1978 | gas phase; At 500K: neutral enol/keto ratio is 1.7:1, Folkendt, Weiss-Lopez, et al., 1989. ΔH=-4.7 kcal/mol, enol favored. Carbonyls anti in anion, via calc: Irikura, 1999; B |
Ion clustering data
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Gas phase ion energetics data, References, Notes
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
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias
Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. Searches may be limited to ion clustering reactions. A general reaction search form is also available.
Clustering reactions
By formula: Cl- + C5H8O2 = (Cl- • C5H8O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrG° | 56.07 | kJ/mol | TDEq | French, Ikuta, et al., 1982 | gas phase; B |
Free energy of reaction
ΔrG° (kJ/mol) | T (K) | Method | Reference | Comment |
---|---|---|---|---|
46.0 | 421. | PHPMS | French, Ikuta, et al., 1982 | gas phase; M |
By formula: I- + C5H8O2 = (I- • C5H8O2)
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 63.2 ± 4.2 | kJ/mol | TDAs | Caldwell, Masucci, et al., 1989 | gas phase; B,M |
References
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Gas phase ion energetics data, Ion clustering data, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Hacking and Pilcher, 1979
Hacking, J.M.; Pilcher, G.,
Enthalpy of combustion of pentane-2,4-dione,
J. Chem. Thermodyn., 1979, 11, 1015-1017. [all data]
Conrath, Van de Sande, et al., 1974
Conrath, k.; Van de Sande, C.; Vandewalle, M.,
Studies in organic mass spectrometry. XVI. A combined approach to the structures of ions generated from the molecular ions of acyclic β-diketones through loss of small neutral molecules,
Org. Mass Spectrom., 1974, 9, 585-593. [all data]
Melia and Merrifield, 1969
Melia, T.P.; Merrifield, R.,
Thermal properties of acetylacetone,
J. Appl. Chem., 1969, 19, 79-82. [all data]
Vilcu and Perisanu, 1979
Vilcu, R.; Perisanu, S.,
The standard enthalpies of formation of some C, H, O containing compounds,
Rev. Roum. Chim., 1979, 24, 237-243. [all data]
Guinchant, 1918
Guinchant, M.J.,
Etude sur la fonction acide dans les derives metheniques et methiniques,
Ann. Chem., 1918, 10, 30-84. [all data]
Nicholson, 1957
Nicholson, G.R.,
The heat of combustion of acetylacetone,
J. Chem. Soc., 1957, 2431-2432. [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]
Houk, Davis, et al., 1973
Houk, K.N.; Davis, L.P.; Newkome, G.R.; Duke, R.E., Jr.; Nauman, R.V.,
Photoelectron spectroscopy of cyclic β-diketones their enolone tautomers,
J. Am. Chem. Soc., 1973, 95, 8364. [all data]
Shigorin, Filyugina, et al., 1967
Shigorin, D.N.; Filyugina, A.D.; Potapov, V.K.,
Role of intramolecular hydrogen bonding in the ionisation and dissociation of compounds,
Zh. Fiz. Khim., 1967, 41, 2336, In original 1255. [all data]
Watanabe, Nakayama, et al., 1962
Watanabe, K.; Nakayama, T.; Mottl, J.,
Ionization potentials of some molecules,
J. Quant. Spectry. Radiative Transfer, 1962, 2, 369. [all data]
Hush, Livett, et al., 1987
Hush, N.S.; Livett, M.K.; Peel, J.B.; Willett, G.D.,
Variable-temperature ultraviolet photoelectron spectroscopy of the keto-enol tautomers of pentane-2,4-dione,
Aust. J. Chem., 1987, 40, 599. [all data]
Cauletti, Furlani, et al., 1980
Cauletti, C.; Furlani, C.; Storto, G.,
Coordinative bond d-shell ionisations in the UV photoelectron spectra of bis({beta}-diketonato) cobalt (II) copper (II) complexes, their thio analogues,
J. Electron Spectrosc. Relat. Phenom., 1980, 18, 329. [all data]
Schweig, Vermeer, et al., 1974
Schweig, A.; Vermeer, H.; Weidner, U.,
A photoelectron spectroscopic study of keto-enol tautomerism in acetylacetones - a new application of photoelectron spectroscopy,
Chem. Phys. Lett., 1974, 26, 229. [all data]
Evans, Hamnett, et al., 1972
Evans, S.; Hamnett, A.; Orchard, A.F.; Lloyd, D.R.,
Study of the metal-oxygen bond in simple tris-chelate complexes by He(I) photoelectron spectroscopy,
Faraday Discuss. Chem. Soc., 1972, 54, 227. [all data]
Reichert and Westmore, 1969
Reichert, C.; Westmore, J.B.,
Mass spectral studies of metal chelates. IV.Mass spectra, appearance potentials, and coordinate bond energies of bis(acetylacetonate)metal(II) complexes of the first transition series,
Inorg. Chem., 1969, 8, 1012. [all data]
Taft and Bordwell, 1988
Taft, R.W.; Bordwell, F.G.,
Structural and Solvent Effects Evaluated from Acidities Measured in Dimethyl Sulfoxide and in the Gas Phase,
Acc. Chem. Res., 1988, 21, 12, 463, https://doi.org/10.1021/ar00156a005
. [all data]
Strohmeier and Höhne, 1952
Strohmeier, W.; Höhne, I.,
Keto-Enol-Umwandlung des Acetylacteons in Gaszustand,
Z. Naturfor., 1952, 7B, 184. [all data]
Cumming and Kebarle, 1978
Cumming, J.B.; Kebarle, P.,
Summary of gas phase measurements involving acids AH. Entropy changes in proton transfer reactions involving negative ions. Bond dissociation energies D(A-H) and electron affinities EA(A),
Can. J. Chem., 1978, 56, 1. [all data]
Folkendt, Weiss-Lopez, et al., 1989
Folkendt, M.M.; Weiss-Lopez, B.E.; Chauvel, J.P., Jr.; True, N.S.,
Gas-Phase 1H NMR Studies of Keto-Enol Tautomerization of Acetylacetone, Methyl Acetoacetate, and Ethyl Acetoacetate,
J. Phys. Chem., 1989, 89, 15, 3347, https://doi.org/10.1021/j100261a038
. [all data]
Irikura, 1999
Irikura, K.K.,
Acetylacetonate (acac) anion in the gas phase: predicted structures, vibrational spectra, and photodetachment energies,
Int. J. Mass Spectrom., 1999, 187, 577-587, https://doi.org/10.1016/S1387-3806(98)14192-1
. [all data]
French, Ikuta, et al., 1982
French, M.A.; Ikuta, S.; Kebarle, P.,
Hydrogen bonding of O-H and C-H hydrogen donors to Cl-. Results from mass spectrometric measurement of the ion-molecule equilibria RH + Cl- = RHCl-,
Can. J. Chem., 1982, 60, 1907. [all data]
Caldwell, Masucci, et al., 1989
Caldwell, G.W.; Masucci, J.A.; Ikonomou, M.G.,
Negative Ion Chemical Ionization Mass Spectrometry - Binding of Molecules to Bromide and Iodide Anions,
Org. Mass Spectrom., 1989, 24, 1, 8, https://doi.org/10.1002/oms.1210240103
. [all data]
Notes
Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Gas phase ion energetics data, Ion clustering data, References
- Symbols used in this document:
AE Appearance energy IE (evaluated) Recommended ionization energy T Temperature ΔcH°liquid Enthalpy of combustion of liquid at standard conditions ΔfH°gas Enthalpy of formation of gas at standard conditions ΔfH°liquid Enthalpy of formation of liquid at standard conditions 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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