2-Amino-3-(4-hydroxyphenyl)-propanoic acid


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: Robert C. Dunbar

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

Sodium ion (1+) + 2-Amino-3-(4-hydroxyphenyl)-propanoic acid = (Sodium ion (1+) • 2-Amino-3-(4-hydroxyphenyl)-propanoic acid)

By formula: Na+ + C9H11NO3 = (Na+ • C9H11NO3)

Quantity Value Units Method Reference Comment
Δr48.0kcal/molCIDCKish, Ohanessian, et al., 2003Anchor alanine=39.89

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:
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

Ionization energy determinations

IE (eV) Method Reference Comment
8.0PECannington and Ham, 1983LBLHLM
≤8.4EIAkopyan and Loginov, 1967RDSH
8.5PECannington and Ham, 1983Vertical value; LBLHLM

Ion clustering 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: Robert C. Dunbar

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. Searches may be limited to ion clustering reactions. A general reaction search form is also available.

Clustering reactions

Sodium ion (1+) + 2-Amino-3-(4-hydroxyphenyl)-propanoic acid = (Sodium ion (1+) • 2-Amino-3-(4-hydroxyphenyl)-propanoic acid)

By formula: Na+ + C9H11NO3 = (Na+ • C9H11NO3)

Quantity Value Units Method Reference Comment
Δr48.0kcal/molCIDCKish, Ohanessian, et al., 2003Anchor alanine=39.89

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.

Kish, Ohanessian, et al., 2003
Kish, M.M.; Ohanessian, G.; Wesdemiotis, C., The Na+ affinities of a-amino acids: side-chain substituent effects, Int. J. Mass Spectrom., 2003, 227, 3, 509, https://doi.org/10.1016/S1387-3806(03)00082-4 . [all data]

Cannington and Ham, 1983
Cannington, P.H.; Ham, N.S., He(I) and He(II) photoelectron spectra of glycine and related molecules, J. Electron Spectrosc. Relat. Phenom., 1983, 32, 139. [all data]

Akopyan and Loginov, 1967
Akopyan, M.E.; Loginov, Yy.V., Mass-spectrometric study of the phoionization of free α-aminoacids, High Energy Chem., 1967, 1, 83, In original 97. [all data]


Notes

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