L-Cysteine anion


Reaction thermochemistry 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 by: John E. Bartmess

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Individual Reactions

C3H6NO2S- + Hydrogen cation = L-Cysteine

By formula: C3H6NO2S- + H+ = C3H7NO2S

Quantity Value Units Method Reference Comment
Δr333.4 ± 2.2kcal/molCIDCJones, Bernier, et al., 2007gas phase
Δr334.3 ± 2.3kcal/molG+TSTian, Pawlow, et al., 2007gas phase; Calcn say SH is 3.1 kcal/mol more acidic than CO2H. See DeBlase, Kass, et al., 2014 for spectroscopy saying that it is a cyclic H-bonded species
Quantity Value Units Method Reference Comment
Δr327.5 ± 2.1kcal/molN/ATian, Pawlow, et al., 2007gas phase; Calcn say SH is 3.1 kcal/mol more acidic than CO2H. See DeBlase, Kass, et al., 2014 for spectroscopy saying that it is a cyclic H-bonded species
Δr326.0 ± 3.0kcal/molCIDCO'Hair, Bowie, et al., 1992gas phase

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 by: John E. Bartmess

Electron affinity of neutral species

EAneutral (eV) Method Reference Comment
4.00 ± 0.16D-EATian, Pawlow, et al., 2007Calcn say SH is 3.1 kcal/mol more acidic than CO2H. See DeBlase, Kass, et al., 2014 for spectroscopy saying that it is a cyclic H-bonded species

Protonation reactions

C3H6NO2S- + Hydrogen cation = L-Cysteine

By formula: C3H6NO2S- + H+ = C3H7NO2S

Quantity Value Units Method Reference Comment
Δr333.4 ± 2.2kcal/molCIDCJones, Bernier, et al., 2007gas phase
Δr334.3 ± 2.3kcal/molG+TSTian, Pawlow, et al., 2007gas phase; Calcn say SH is 3.1 kcal/mol more acidic than CO2H. See DeBlase, Kass, et al., 2014 for spectroscopy saying that it is a cyclic H-bonded species
Quantity Value Units Method Reference Comment
Δr327.5 ± 2.1kcal/molN/ATian, Pawlow, et al., 2007gas phase; Calcn say SH is 3.1 kcal/mol more acidic than CO2H. See DeBlase, Kass, et al., 2014 for spectroscopy saying that it is a cyclic H-bonded species
Δr326.0 ± 3.0kcal/molCIDCO'Hair, Bowie, et al., 1992gas phase

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Jones, Bernier, et al., 2007
Jones, C.M.; Bernier, M.; Carson, E.; Colyer, K.E.; Metz, R.; Pawlow, A.; Wischow, E.D.; Webb, I.; Andriole, E.J.; Poutsma, J.C., Gas-phase Acities of the 20 Protein Amino Acids, Int. J. Mass Spectrom., 2007, 267, 1-3, 54-62, https://doi.org/10.1016/j.ijms.2007.02.018 . [all data]

Tian, Pawlow, et al., 2007
Tian, Z.X.; Pawlow, A.; Poutsma, J.C.; Kass, S.R., Are carboxyl groups the most acidic sites in amino acids? Gas-phase acidity, H/D exchange experiments, and computations on cysteine and its conjugate base, J. Am. Chem. Soc., 2007, 129, 17, 5403-5407, https://doi.org/10.1021/ja0666194 . [all data]

DeBlase, Kass, et al., 2014
DeBlase, A.F.; Kass, S.R.; Johnson, M.A., On the character of the cyclic ionic H-bond in cryogenically cooled deprotonated cysteine, Phys. Chem. Chem. Phys., 2014, 16, 10, 4569-4575, https://doi.org/10.1039/c3cp54117g . [all data]

O'Hair, Bowie, et al., 1992
O'Hair, R.J.; Bowie, J.H.; Gronert, S., Gas Phase Acidity of the alpha-Amino Acids, Int. J. Mass Spectrom. Ion Proc., 1992, 117, 23, https://doi.org/10.1016/0168-1176(92)80083-D . [all data]


Notes

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