C6H5O+ (structure unspecified)
- Formula: C6H5O+
- Molecular weight: 93.1028
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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.
Reactions leading to C6H5O+ (ion structure unspecified)
| Precursor | AP (eV) | Other Products | Method | Reference | Comment |
|---|---|---|---|---|---|
| C6H5BrO | 12.17 | Br | EI | Howe and Williams, 1969 | |
| C6H5NO2 | 10.68 ± 0.35 | NO | CAD | Katritzky, Watson, et al., 1990 | |
| C6H5NO2 | 10.89 ± 0.04 | NO | PIPECO | Nishimura, Das, et al., 1986 | |
| C6H5NO2 | 10.98 ± 0.05 | NO | PIPECO | Panczel and Baer, 1984 | T = 298K |
| C6H5NO2 | 11.12 ± 0.05 | NO | PIPECO | Panczel and Baer, 1984 | T = 0K |
| C6H5NO2 | 10.95 ± 0.05 | NO | PI | Matyuk, Potapov, et al., 1979 | |
| C6H5NO2 | 10.4 ± 0.1 | NO | EI | Brown, 1970 | |
| C6H5NO3 | 11.9 ± 0.1 | NO2 | EI | Brown, 1970 | |
| C7H5ClO | 10.18 | Cl | EI | Elder, Beynon, et al., 1976 | |
| C7H6O3 | 14.4 ± 0.2 | CO+OH | EI | Benoit, 1973 | |
| C7H6O3 | 14.6 ± 0.2 | CO+OH | EI | Benoit, 1973 | |
| C7H8O | 11.70 ± 0.05 | CH3 | PI | Ponomarev, Arapov, et al., 1986 | |
| C7H8O | 11.9 ± 0.1 | CH3 | PIPECO | Das, Gilman, et al., 1986 | |
| C7H8O | 11.3 | CH3 | EI | McLafferty, Bente, et al., 1973 | |
| C7H8O | 11.8 ± 0.1 | CH3 | EI | Brown, 1970, 2 | |
| C7H8O | 11.9 ± 0.1 | CH3 | EI | Fisher, Palmer, et al., 1964 | |
| C7H8O | 11.9 ± 0.1 | CH3 | EI | Tait, Shannon, et al., 1962 | |
| C8H6O | 9.5 ± 0.1 | C2H | EI | Coats and Anderson, 1957 |
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.
Howe and Williams, 1969
Howe, I.; Williams, D.H.,
Calculation and qualitative predictions of mass spectra. Mono- and paradisubstituted benzenes,
J. Am. Chem. Soc., 1969, 91, 7137. [all data]
Katritzky, Watson, et al., 1990
Katritzky, A.R.; Watson, C.H.; Dega-Szafran, Z.; Eyler, J.R.,
Collisionally activated dissociation of N-alkylpyridinium cations to pyridine and alkyl cations in the gas phase,
J. Am. Chem. Soc., 1990, 112, 2471. [all data]
Nishimura, Das, et al., 1986
Nishimura, T.; Das, P.R.; Meisels, G.G.,
On the dissociation dynamics of energy-selected nitrobenzene ion,
J. Chem. Phys., 1986, 84, 6190. [all data]
Panczel and Baer, 1984
Panczel, M.; Baer, T.,
A photoelectron photoion coincidence (PEPICO) study of fragmentation rates and linetic energy release distributions in nitrobenzene,
Int. J. Mass Spectrom. Ion Processes, 1984, 58, 43. [all data]
Matyuk, Potapov, et al., 1979
Matyuk, V.M.; Potapov, V.K.; Prokhoda, A.L.,
Photoexcitation and photoionisation of nitro- derivatives of benzene and toluene,
Russ. J. Phys. Chem., 1979, 53, 538. [all data]
Brown, 1970
Brown, P.,
Kinetic studies in mass spectrometry. IX. Competing [M-NO2] and [M-NO] reactions in substituted nitrobenzenes. Approximate activation energies from ionization and appearance potentials,
Org. Mass Spectrom., 1970, 4, 533. [all data]
Elder, Beynon, et al., 1976
Elder, J.F.; Beynon, J.H.; Cooks, R.G.,
The benzoyl ion. Thermochemistry and kinetic energy release,
Org. Mass Spectrom., 1976, 11, 415. [all data]
Benoit, 1973
Benoit, F.,
Substituent effects in mass spectrometry. III. Substituent effects in the dissociation of the molecular ions of para and meta subtituted benzoic acids,
Org. Mass Spectrom., 1973, 7, 295. [all data]
Ponomarev, Arapov, et al., 1986
Ponomarev, D.A.; Arapov, O.V.; Sergeev, Y.L.; Chistyakov, A.B.,
[Title unavailable],
Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol., 1986, 29, 107. [all data]
Das, Gilman, et al., 1986
Das, P.R.; Gilman, J.P.; Meisels, G.G.,
Unimolecular decomposition of energy-selected anisole ions. Breakdown graph and metastable decay rates,
Int. J. Mass Spectrom. Ion Processes, 1986, 68, 155. [all data]
McLafferty, Bente, et al., 1973
McLafferty, F.W.; Bente, P.F., III; Kornfeld, R.; Tsai, S.-C.; Howe, I.,
Collisional activation spectra of organic ions,
J. Am. Chem. Soc., 1973, 95, 2120. [all data]
Brown, 1970, 2
Brown, P.,
Kinetic studies in mass spectrometry. VIII. Competing [M-CH3] and [M-CH2O] reactions in substituted anisoles. Approximate activation energies from ionization appearance potentials,
Org. Mass Spectrom., 1970, 4, 519. [all data]
Fisher, Palmer, et al., 1964
Fisher, I.P.; Palmer, T.F.; Lossing, F.P.,
The vertical ionization potentials of phenyl and phenoxy radicals,
J. Am. Chem. Soc., 1964, 86, 2741. [all data]
Tait, Shannon, et al., 1962
Tait, J.M.S.; Shannon, T.W.; Harrison, A.G.,
The structure of substituted C7 ions from benzyl derivatives at the appearance potential threshold,
J. Am. Chem. Soc., 1962, 84, 4. [all data]
Coats and Anderson, 1957
Coats, F.H.; Anderson, R.C.,
Thermodynamic data from electron-impact measurements on acetylene and substituted acetylenes,
J. Am. Chem. Soc., 1957, 79, 1340. [all data]
Notes
Go To: Top, Gas phase ion energetics data, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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