1,3,5,7-Cyclooctatetraene
- Formula: C8H8
- Molecular weight: 104.1491
- IUPAC Standard InChIKey: KDUIUFJBNGTBMD-BONZMOEMSA-N
- CAS Registry Number: 629-20-9
- 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: [8]Annulene; Cyclooctatetraene; UN 2358
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Gas phase thermochemistry data
Go To: Top, Gas phase ion energetics data, Mass spectrum (electron ionization), 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:
DRB - Donald R. Burgess, Jr.
GT - Glushko Thermocenter, Russian Academy of Sciences, Moscow
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔfH°gas | 71.13 ± 0.31 | kcal/mol | N/A | Prosen, Johnson, et al., 1950 | Value computed using ΔfHliquid° value of 254.5±1.3 kj/mol from Prosen, Johnson, et al., 1950 and ΔvapH° value of 43.1±0.31 kj/mol from missing citation.; DRB |
Quantity | Value | Units | Method | Reference | Comment |
S°gas | 78.10 ± 0.35 | cal/mol*K | N/A | Scott D.W., 1949 | GT |
Constant pressure heat capacity of gas
Cp,gas (cal/mol*K) | Temperature (K) | Reference | Comment |
---|---|---|---|
8.564 | 50. | Dorofeeva O.V., 1986 | Selected values of Cp(T) are in close agreement with those calculated by [ Lippincott E.R., 1951], while the S(T) values are 1.5-2.0 J/mol*K larger than obtained by [ Lippincott E.R., 1951].; GT |
12.11 | 100. | ||
15.90 | 150. | ||
20.03 | 200. | ||
26.883 | 273.15 | ||
29.30 ± 0.84 | 298.15 | ||
29.484 | 300. | ||
38.678 | 400. | ||
46.465 | 500. | ||
52.811 | 600. | ||
57.995 | 700. | ||
62.292 | 800. | ||
65.894 | 900. | ||
68.939 | 1000. | ||
71.532 | 1100. | ||
73.745 | 1200. | ||
75.645 | 1300. | ||
77.280 | 1400. | ||
78.695 | 1500. |
Gas phase ion energetics data
Go To: Top, Gas phase thermochemistry data, Mass spectrum (electron ionization), 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
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
View reactions leading to C8H8+ (ion structure unspecified)
Electron affinity determinations
EA (eV) | Method | Reference | Comment |
---|---|---|---|
0.570 ± 0.030 | N/A | Miller, Viggiano, et al., 2002 | B |
0.550 ± 0.020 | IMRE | Kato, Lee, et al., 1997 | B |
0.650 ± 0.043 | LPES | Wenthold, Hrovat, et al., 1996 | EA(D4h COT) = 1.099 ± 0.01 eV. D4H is TS, 10-11 kcal/mol above GS D8h; B |
0.58 ± 0.10 | CIDC | Denault, Chen, et al., 1998 | entropy of attachment: -14.7±13 eu; B |
<0.823919 | PD | Gygax, Peters, et al., 1979 | B |
0.577 ± 0.043 | ECD | Wentworth and Ristau, 1969 | B |
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
8.03 | PE | Fu and Dunbar, 1978 | LLK |
8.0 | PE | Batich, Bischof, et al., 1973 | LLK |
8.21 | PE | Dewar, Harget, et al., 1969 | Unpublished result of M.J.S. Dewar and S.D. Worley; RDSH |
8.04 | PE | Al-Joboury and Turner, 1964 | RDSH |
7.99 ± 0.02 | PI | Watanabe, Nakayama, et al., 1962 | RDSH |
8.43 | PE | Fu and Dunbar, 1978 | Vertical value; LLK |
Appearance energy determinations
Ion | AE (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C3H3+ | 13.40 ± 0.10 | ? | EI | Franklin and Carroll, 1969 | RDSH |
C4H2+ | 17.11 ± 0.10 | 2C2H2+H2 | EI | Franklin and Carroll, 1969 | RDSH |
C4H3+ | 18.16 ± 0.25 | 2C2H2+H | EI | Franklin and Carroll, 1969 | RDSH |
C4H4+ | 15.10 ± 0.10 | 2C2H2 | EI | Franklin and Carroll, 1969 | RDSH |
C5H3+ | 16.41 ± 0.15 | C2H2+CH3? | EI | Franklin and Carroll, 1969 | RDSH |
C6H5+ | 14.58 ± 0.10 | C2H2+H | EI | Franklin and Carroll, 1969 | RDSH |
C6H6+ | 9.4 ± 0.05 | C2H2 | TRPI | Lifshitz and Malinovich, 1984 | LBLHLM |
C6H6+ | 9.70 ± 0.12 | C2H2 | EI | Franklin and Carroll, 1969 | RDSH |
C8H6+ | 11.70 ± 0.10 | H2 | EI | Franklin and Carroll, 1969 | RDSH |
C8H7+ | 10.90 ± 0.10 | H | EI | Franklin and Carroll, 1969 | RDSH |
De-protonation reactions
C8H7- + =
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
ΔrH° | 382.7 ± 2.8 | kcal/mol | G+TS | Kato, Lee, et al., 1997 | gas phase; B |
Quantity | Value | Units | Method | Reference | Comment |
ΔrG° | 374.8 ± 2.5 | kcal/mol | IMRE | Kato, Lee, et al., 1997 | gas phase; B |
Mass spectrum (electron ionization)
Go To: Top, Gas 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 by: NIST Mass Spectrometry Data Center, William E. Wallace, director
Spectrum
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Additional Data
View image of digitized spectrum (can be printed in landscape orientation).
Due to licensing restrictions, this spectrum cannot be downloaded.
Owner | NIST Mass Spectrometry Data Center Collection (C) 2014 copyright by the U.S. Secretary of Commerce on behalf of the United States of America. All rights reserved. |
---|---|
NIST MS number | 1259 |
References
Go To: Top, Gas phase thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Prosen, Johnson, et al., 1950
Prosen, E.J.; Johnson, W.H.; Rossini, F.D.,
Heat of combustion and formation of 1,3,5,7-cyclooctatetraene and its heat of isomerization of styrene,
J. Am. Chem. Soc., 1950, 72, 626-629. [all data]
Scott D.W., 1949
Scott D.W.,
Cyclooctatetraene: low-temperature heat capacity, heat of fusion, heat of vaporization, vapor pressure, and entropy,
J. Am. Chem. Soc., 1949, 71, 1634-1636. [all data]
Dorofeeva O.V., 1986
Dorofeeva O.V.,
Thermodynamic properties of twenty-one monocyclic hydrocarbons,
J. Phys. Chem. Ref. Data, 1986, 15, 437-464. [all data]
Lippincott E.R., 1951
Lippincott E.R.,
The thermodynamic functions of cyclooctatetraene,
J. Am. Chem. Soc., 1951, 73, 3889-3891. [all data]
Miller, Viggiano, et al., 2002
Miller, T.M.; Viggiano, A.A.; Miller, A.E.S.,
Electron attachment and detachment: Cyclooctatetraene,
J. Phys. Chem. A, 2002, 106, 43, 10200-10204, https://doi.org/10.1021/jp0205214
. [all data]
Kato, Lee, et al., 1997
Kato, S.; Lee, H.S.; Gareyev, R.; Wenthold, P.G.; Lineberger, W.C.; DePuy, C.H.; Bierbaum, V.M.,
Experimental and Computational Studies of the Structures and Energetics of Cyclooctatetraene and Its Derivatives,
J. Am. Chem. Soc., 1997, 119, 33, 7863, https://doi.org/10.1021/ja971433d
. [all data]
Wenthold, Hrovat, et al., 1996
Wenthold, P.G.; Hrovat, D.A.; Borden, W.T.; Lineberger, W.C.,
Transition State Spectroscopy of Cyclooctatetraene,
Science, 1996, 272, 5267, 1456, https://doi.org/10.1126/science.272.5267.1456
. [all data]
Denault, Chen, et al., 1998
Denault, J.W.; Chen, G.D.; Cooks, R.G.,
Electron affinity of 1,3,5,7-cyclooctatetraene determined by the kinetic method,
J. Am. Soc. Mass Spectrom., 1998, 9, 11, 1141-1145, https://doi.org/10.1016/S1044-0305(98)00092-0
. [all data]
Gygax, Peters, et al., 1979
Gygax, R.; Peters, H.L.; Brauman, J.I.,
Photodetachment of electrons from anions of high symmetry. Electron photodetachment spectra of the cycloctatetraenyl and perinaphthenyl anions,
J. Am. Chem. Soc., 1979, 101, 2567. [all data]
Wentworth and Ristau, 1969
Wentworth, W.E.; Ristau, W.,
Thermal Electron Attachment Involving a Change in Molecular Geometry,
J. Phys. Chem., 1969, 73, 7, 2126, https://doi.org/10.1021/j100727a005
. [all data]
Fu and Dunbar, 1978
Fu, E.W.; Dunbar, R.C.,
Photodissociation spectroscopy and structural rearrangements in ions of cyclooctatetraene, styrene and related molecules,
J. Am. Chem. Soc., 1978, 100, 2283. [all data]
Batich, Bischof, et al., 1973
Batich, C.; Bischof, P.; Heilbronner, E.,
The photoelectron spectra of cyclooctatetraene and its hydrogenated derivatives,
J. Electron Spectrosc. Relat. Phenom., 1973, 1, 333. [all data]
Dewar, Harget, et al., 1969
Dewar, M.J.S.; Harget, A.; Haselbach, E.,
Cyclooctatetraene and ions derived from it,
J. Am. Chem. Soc., 1969, 91, 7521. [all data]
Al-Joboury and Turner, 1964
Al-Joboury, M.I.; Turner, D.W.,
Molecular photoelectron spectroscopy. Part II. A summary of ionization potentials,
J. Chem. Soc., 1964, 4434. [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]
Franklin and Carroll, 1969
Franklin, J.L.; Carroll, S.R.,
The effect of molecular structure on ionic decomposition. I. An electron impact study of seven C8H8 isomers,
J. Am. Chem. Soc., 1969, 91, 5940. [all data]
Lifshitz and Malinovich, 1984
Lifshitz, C.; Malinovich, Y.,
Time resolved photoionization mass spectrometry in the millisecond range,
Int. J. Mass Spectrom. Ion Processes, 1984, 60, 99. [all data]
Notes
Go To: Top, Gas phase thermochemistry data, Gas phase ion energetics data, Mass spectrum (electron ionization), References
- Symbols used in this document:
AE Appearance energy Cp,gas Constant pressure heat capacity of gas EA Electron affinity S°gas Entropy of gas at standard conditions ΔfH°gas Enthalpy of formation of gas 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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