C2H2S+ (structure unspecified)
- Formula: C2H2S+
- Molecular weight: 58.102
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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 C2H2S+ (ion structure unspecified)
Precursor | AP (eV) | Other Products | Method | Reference | Comment |
---|---|---|---|---|---|
C2H4S | 15.0 ± 0.2 | ? | EI | Gallegos and Kiser, 1961 | |
C2H6OS | 13. ± 0.3 | ? | EI | Blais, Cottin, et al., 1970 | |
C2H6S2 | 10.15 ± 0.08 | CH3SH | PIPECO | Butler, Baer, et al., 1983 | T = 298K |
C3H6S | 15.6 ± 0.4 | ? | EI | Hobrock and Kiser, 1962 | |
C4H4S | 12.5 ± 0.2 | C2H2 | CEMS | Tedder and Vidaud, 1980 | |
C4H4S | 12.1 ± 0.1 | C2H2 | PE | Butler and Baer, 1980 | |
C4H4S | 10.8 ± 0.2 | ? | EI | Khvostenko, 1962 | |
C4H8S | 17.0 ± 0.3 | ? | EI | Gallegos and Kiser, 1962 | |
C4H10S2 | 18.6 ± 0.5 | ? | EI | Hobrock and Kiser, 1963 | |
C5H6S | 12.3 ± 0.3 | ? | EI | Bogolyubov, Plotnikov, et al., 1969 | |
C6H8S | 12.1 ± 0.3 | ? | EI | Bogolyubov, Plotnikov, et al., 1969 |
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.
Gallegos and Kiser, 1961
Gallegos, E.; Kiser, R.W.,
Electron impact spectroscopy of ethylene sulfide and ethylenimine,
J. Phys. Chem., 1961, 65, 1177. [all data]
Blais, Cottin, et al., 1970
Blais, J.-C.; Cottin, M.; Gitton, B.,
Ionisation positive et negative dans le dimethylsulfoxyde en phase gazeuse,
J. Chim. Phys., 1970, 67, 1475. [all data]
Butler, Baer, et al., 1983
Butler, J.J.; Baer, T.; Evans, S.A., Jr.,
Energetics and structures of organosulfur ions: CH3SSCH3+, CH3SS+, C2H5S+, and CH2SH+,
J. Am. Chem. Soc., 1983, 105, 3451. [all data]
Hobrock and Kiser, 1962
Hobrock, B.G.; Kiser, R.W.,
Electron impact spectroscopy of propylene sulfide,
J. Phys. Chem., 1962, 66, 1551. [all data]
Tedder and Vidaud, 1980
Tedder, J.M.; Vidaud, P.H.,
Charge exchange mass spectra of thiophene, pyrrole and furan,
J. Chem. Soc. Faraday Trans. 2, 1980, 76, 1516. [all data]
Butler and Baer, 1980
Butler, J.J.; Baer, T.,
Thermochemistry and dissociation dynamics of state-selected C4H4X ions. 1. Thiophene,
J. Am. Chem. Soc., 1980, 102, 6764. [all data]
Khvostenko, 1962
Khvostenko, V.I.,
Ionisation of thiophen and some of its derivatives by electron impact,
Zh. Fiz. Khim., 1962, 36, 384, In original 197. [all data]
Gallegos and Kiser, 1962
Gallegos, E.J.; Kiser, R.W.,
Electron impact spectroscopy of the four- and five-membered, saturated heterocyclic compounds containing nitrogen, oxygen and sulfur,
J. Phys. Chem., 1962, 66, 136. [all data]
Hobrock and Kiser, 1963
Hobrock, B.G.; Kiser, R.W.,
Electron impact investigations of sulfur compounds. II. 3-Methyl-2-thiabutane, 4-thia-1-pentene, and 3,4-dithiahexane,
J. Phys. Chem., 1963, 67, 648. [all data]
Bogolyubov, Plotnikov, et al., 1969
Bogolyubov, G.M.; Plotnikov, V.F.; Boiko, Yu.A.; Petrov, A.A.,
Organic derivatives of elements of groups V and VI. IX. Mass spectra of vinylacetylene sulfides,
Zh. Obshch. Khim., 1969, 39, 2467, In original 2407. [all data]
Notes
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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