Phenylthio radical
- Formula: C6H5S
- Molecular weight: 109.169
- CAS Registry Number: 4985-62-0
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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.
Data compiled as indicated in comments:
B - John E. Bartmess
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron
View reactions leading to C6H5S+ (ion structure unspecified)
Electron affinity determinations
| EA (eV) | Method | Reference | Comment |
|---|---|---|---|
| 2.34520 ± 0.00060 | N/A | Kim, Yacovitch, et al., 2011 | B |
| 2.46 ± 0.10 | D-EA | Taft and Bordwell, 1988 | B |
| <2.470 ± 0.060 | PD | Richardson, Stephenson, et al., 1975 | B |
Ionization energy determinations
| IE (eV) | Method | Reference | Comment |
|---|---|---|---|
| 8.6 ± 0.1 | EI | Palmer and Lossing, 1962 | RDSH |
Anion protonation reactions
+
=
By formula: C6H5S- + H+ = C6H6S
| Quantity | Value | Units | Method | Reference | Comment |
|---|---|---|---|---|---|
| ΔrH° | 1424. ± 8.8 | kJ/mol | G+TS | Taft and Bordwell, 1988 | gas phase; B |
| ΔrH° | >1423. ± 7.5 | kJ/mol | D-EA | Richardson, Stephenson, et al., 1975 | gas phase; B |
| Quantity | Value | Units | Method | Reference | Comment |
| ΔrG° | 1395. ± 8.8 | kJ/mol | IMRE | Guillemin, Riague, et al., 2005 | gas phase; B |
| ΔrG° | 1397. ± 8.4 | kJ/mol | IMRE | Taft and Bordwell, 1988 | gas phase; B |
| ΔrG° | >1395. ± 7.9 | kJ/mol | H-TS | Richardson, Stephenson, et al., 1975 | gas phase; B |
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.
Kim, Yacovitch, et al., 2011
Kim, J.B.; Yacovitch, T.I.; Hock, C.; Neumark, D.M.,
Slow photoelectron velocity-map imaging spectroscopy of the phenoxide and thiophenoxide anions,
Phys. Chem. Chem. Phys., 2011, 13, 38, 17378-17383, https://doi.org/10.1039/c1cp22211b
. [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]
Richardson, Stephenson, et al., 1975
Richardson, J.H.; Stephenson, L.M.; Brauman, J.I.,
Photodetachment of electrons from phenoxides and thiophenoxide,
J. Am. Chem. Soc., 1975, 97, 2967. [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]
Guillemin, Riague, et al., 2005
Guillemin, J.C.; Riague, E.H.; Gal, J.F.; Maria, P.C.; Mo, O.; Yanez, M.,
Acidity trends in alpha,beta-unsaturated sulfur, selenium, and tellurium derivatives: Comparison with C-, Si-, Ge-, Sn-, N-, P-, As-, and Sb-containing analogues,
Chem. Eur. J., 2005, 11, 7, 2145-2153, https://doi.org/10.1002/chem.200400989
. [all data]
Notes
Go To: Top, Gas phase ion energetics data, References
- Symbols used in this document:
EA Electron affinity 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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