Hydroxysulfinyl radical and sulfinic acid are stable species in the gas phase

Journal of the American Chemical Society

Volumn 118, Issue 45, 1996, Pages 11321-11322

  Frank, Aaron J ^a   Sadflek, Martin ^a   Ferner, Jordan G ^a   Tureček, Frantis̀ek ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SULFIDE; SULFINIC ACID DERIVATIVE;

ARTICLE; DRUG STABILITY;

EID: 0029860417     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja961922y     Document Type: Article

References (24)

1. (a) Tyndall, G. S.; Ravishankara, A. R. Im. J. Chem. Kinet. 1991, 23, 483.
2. (b) Charlson, R. J.; Wigley, T. M. L. Sei. Am. 199-4, 270, 48.
3. (a) Plummer, P. L. M. J. Chem. Phys. 1990, 92, 6627.
4. (b) Xantheas, S. S.; Dunning, T. H., Jr. J. Phys. Chem. 1993, 97, 6616.
5. (a) Calvert, J. G.; Lazrus, A.; Kok, G. L.; Heikes, B. G.; Walega, J. G.; Lind, J.; Cantrell, C. A. Nature 1985,317,27.
6. (b) Egsgaard, H.; Carlsen, L.; Florension, H.; Drewello, T.; Schwarz, H. Chem. Phys. Lett. 1988,148, 537.
7. Iraqi, M.; Goldberg, N.; Schwarz, H. J. Phys. Chem. 1994, 98, 2015.
8. Iraqi, M.; Schwarz, H. Chem. Phys. Lett. 1994, 227, 359.
9. (a) Laakso, D.; Marshall, P. J. Phys. Chem. 1992, 96, 2471.
10. (b) Laakso, D.; Smith, C. E.; Goumri, A.; Rocha, J.-D. R.; Marshall, P. Chem. Phys. Lett. 1994, 227, 377.
11. Goumri, A.; Rocha, J.-D. R.; Marshall, P. J. Phys. Chem. 1995, 99, 10834.
12. For recent reviews, see: (a) Holmes, J. L. Mass Spectrom. Rev. 1989, 8, 513.
13. (b) Goldberg, N.; Schwarz, H. Acc. Chem. Res. 1994, 27, 347.
14. Turecek, F.; Gu, M.; Shaffer, S. A. J. Am. Soc. Mass Spectrom. 1992, 3, 493.
15. Shaffer, S. A.; Turecek, F.; Cerny, R. L. J. Am. Chem. Soc. 1993, 115, 12117.
16. Kuhns, D. W.; Shaffer, S. A.; Tran, T. B.; Turecek, F. J. Phys. Chem. 1994, 98, 4845.
17. Harrison, A. G. Chemical lonization Mass Spectrometry, 2nd ed.; CRC Press: Boca Raton, FL, 1992.
18. Curtiss, L. A.; Raghavachari, K.; Pople, J. A. J. Chem. Phys. 1993, 95, 1293.
19. Gaussian 2(MP2) energies were obtained from effective QCISD-(T)/6-311+G(3df,2p) calculations (ref 10) using fully optimized MP2-(FULL)/6-31+G(d,p) geometries (ref 12) and including zero-point and 298K corrections obtained from MP2(FULL)/6-31 +G(d,p) harmonic frequen-cies scaled by 0.93. Calculational details will be reported separately.
20. Turecek, F.; Cramer, C. J. J. Am. Chem. Soc. 1995, 117, 12243.
21. . (39.0), OOH- (10.5), H2O (-241.8). See: Lias, S. G.; Bartmess, J. E.; Liebman, J. F.; Holmes. J. L.; Levin, R. D.; Mallard, G. W. J. Phys. Chem. Kef. Data 1988, 17, Supplement 1.
22. Szulejko, J. A.; McMahon, T. B. J. Am.' Chem. Soc. 1993, 115, 7839.
23. (a) Zeller, L.; Farrell, J., Jr.; Vainiotalo, P.; Kemtamaa, H. I. J. Am. Chem. Soc. 1992, 114, 1205.
24. (b) Turecek, F.; Gu, M.; Hop, C. E. C. A. J. Phys. Chem. 1995, 99, 2278.