CH3S+ (structure unspecified)
- Formula: CH3S+
- Molecular weight: 47.099
- Information on this page:
- Options:
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.
Reactions leading to CH3S+ (ion structure unspecified)
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.
Nourbakhsh, Norwood, et al., 1991
Nourbakhsh, S.; Norwood, K.; Yin, H.-M.; Liao, C.-L.; Ng, C.Y.,
Vacuum ultraviolet photodissociation and photoionization studies of CH3SH and SH,
J. Chem. Phys., 1991, 95, 946. [all data]
Holmes, Lossing, et al., 1983
Holmes, J.L.; Lossing, F.P.; Terlouw, J.K.; Burgers, P.C.,
Novel gas-phase ions. The radical cations [CH2XH]+. (X = F, Cl, Br, I, OH, NH2, SH) and [CH2CH2NH3]+.,
Can. J. Chem., 1983, 61, 2305. [all data]
Kutina, Edwards, et al., 1982
Kutina, R.; Edwards, A.; Goodman, G.; Berkowitz, J.,
Photoionization mass spectrometry of CH3SH, CD3SH, and CH3SD: Heats of formation of CH3S+ (CH2SH+), CH2S+, CH2S, and HCS+,
J. Chem. Phys., 1982, 77, 5508. [all data]
Akopyan, Sergeev, et al., 1970
Akopyan, M.E.; Sergeev, Yu.L.; Vilesov, F.I.,
Photionization in vapors of aliphatic sulfides. I. Methymercaptan, dimethyl and diethyl sulfides,
High Energy Chem., 1970, 4, 265, In original 305. [all data]
Taft, Martin, et al., 1965
Taft, R.W.; Martin, R.H.; Lampe, F.W.,
Stabilization energies of substituted methyl cations. The effect of strong demand on the resonance order,
J. Am. Chem. Soc., 1965, 87, 2490. [all data]
Gowenlock, Kay, et al., 1963
Gowenlock, B.G.; Kay, J.; Majer, J.R.,
Electron impact studies of some sulphides and disulphides,
J. Chem. Soc. Faraday Trans., 1963, 59, 2463. [all data]
Hagenow, Jochims, et al., 1989
Hagenow, G.; Jochims, H.-W.; Sawatzki, J.; Minkwitz, R.; Baumgartel, H.,
Photoionisationsmassenspektren von methyl(trifluormethyl)sulfan CH3SCF3,
Z. Naturforsch. B:, 1989, 44, 17. [all data]
Cullen, Frost, et al., 1970
Cullen, W.R.; Frost, D.C.; Pun, M.T.,
Mass spectra, appearance potentials, heats of formation, and bond energies of some alkyl and perfluoroalkyl sulfides,
Inorg. Chem., 1970, 9, 1976. [all data]
Zha, Nishimura, et al., 1988
Zha, Q.; Nishimura, T.; Meisels, G.G.,
Unimolecular dissociation of energy-selected dimethyl sulfoxide,
Int. J. Mass Spectrom. Ion Processes, 1988, 83, 1. [all data]
Amos, Gillis, et al., 1969
Amos, D.; Gillis, R.G.; Occolowitz, J.L.; Pisani, J.F.,
The ions [CH3S]+, [C2H5S]+ and [CH3O]+ formed by electron-impact,
Org. Mass Spectrom., 1969, 2, 209. [all data]
Keyes and Harrson, 1968
Keyes, B.G.; Harrson, A.G.,
The fragmentation of aliphatic sulfur compounds by electron impact,
J. Am. Chem. Soc., 1968, 90, 5671. [all data]
Ermolenko, Akopyan, et al., 1983
Ermolenko, A.I.; Akopyan, M.E.; Sergeev, Y.L.,
Decomposition of dimethyl sulfide molecular ions. Randomization of states during photoionization dissociation of molecules,
High Energy Chem., 1983, 17, 25. [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]
Palmer and Lossing, 1962
Palmer, T.F.; Lossing, F.P.,
Free radicals by mass spectrometry. XXVIII. The HS, CH3S, and phenyl-S radicals: ionization potentials and heats of formation,
J. Am. Chem. Soc., 1962, 84, 4661. [all data]
Hobrock and Kiser, 1963
Hobrock, B.G.; Kiser, R.W.,
Electron impact investigations of sulfur compounds. III. 2-Thiapropane, 3-thiapentane, and 2,3,4-trithiapentane,
J. Phys. Chem., 1963, 67, 1283. [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]
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]
Conde-Caprace and Collin, 1972
Conde-Caprace, G.; Collin, J.E.,
Ionization and dissociation of cyclic ethers thioethers by electron-impact. A comparison between 1,3-dioxolane, 1,3-dithiolane and 1,3-oxathiolane,
Org. Mass Spectrom., 1972, 6, 415. [all data]
Potzinger, Stracke, et al., 1975
Potzinger, P.; Stracke, H.-U.; Kupper, W.; Gollnick, K.,
Ionisierungs- und Auftrittspotentialmessungen an Dialkylsulfoxiden,
Z. Naturforsch. A:, 1975, 30, 340. [all data]
Hobrock and Kiser, 1962, 2
Hobrock, B.G.; Kiser, R.W.,
Electron impact spectroscopy of sulfur compounds. I. 2-Thiabutane, 2-thiapentane, and 2,3-dithiabutane,
J. Phys. Chem., 1962, 66, 1648. [all data]
Santoro, 1973
Santoro, E.,
The fragmentation of some alkyl thiophosphate esters by electron-impact,
Org. Mass Spectrom., 1973, 7, 589. [all data]
Conde-Caprace and Collin, 1969
Conde-Caprace, G.; Collin, J.E.,
Ionization and dissociation of cyclic ethers and thioethers by electronimpact. A comparison between 1,4 dioxane, 1,4 dithiane and 1,4 oxathiane,
Org. Mass Spectrom., 1969, 2, 1277. [all data]
Hobrock and Kiser, 1963, 2
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]
Butler and Baer, 1983
Butler, J.J.; Baer, T.,
A photoionization study of organosulfur ring compounds: Thiirane, thietane and tetrahydrothiophene,
Org. Mass Spectrom., 1983, 18, 248. [all data]
Gal'perin, Bogolyubov, et al., 1969
Gal'perin, Ya.V.; Bogolyubov, G.M.; Grishin, N.N.; Petrov, A.A.,
Organic derivatives of elements of groups V and VI. VI. Mass spectra of compounds with S-S bonds,
Zh. Obshch. Khim., 1969, 39, 1599, In original 1567. [all data]
Svec and Junk, 1967
Svec, H.J.; Junk, G.A.,
Electron-impact studies of substituted alkanes,
J. Am. Chem. Soc., 1967, 89, 790. [all data]
Broer and Weringa, 1980
Broer, W.J.; Weringa, W.D.,
Potential energy profiles for the unimolecular reactions of [C3H7S]+ ions,
Org. Mass Spectrom., 1980, 15, 229. [all data]
Notes
Go To: Top, Gas phase ion energetics data, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
- The National Institute of Standards and Technology (NIST) uses its best efforts to deliver a high quality copy of the Database and to verify that the data contained therein have been selected on the basis of sound scientific judgment. However, NIST makes no warranties to that effect, and NIST shall not be liable for any damage that may result from errors or omissions in the Database.
- Customer support for NIST Standard Reference Data products.