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Science 9 December 1994:
Vol. 266. no. 5191, pp. 1665 - 1668
DOI: 10.1126/science.266.5191.1665

Articles

Symmetries of Hydrogen Bonds in Solution

Charles L. Perrin 1

1 Department of Chemistry, University of California at San Diego, La Jolla, CA 92093-0358, USA.

The nuclear magnetic resonance method of isotopic perturbation can distinguish between single- and double-well potentials in intramolecularly hydrogen-bonded monoanions of dicarboxylic acids. These are classic cases of a "strong," symmetric hydrogen bond in the crystal. The observed carbon-13 isotope shifts induced by the substitution of oxygen-18 demonstrate that these monoanions exist as a single symmetric structure in a nonpolar solvent but as two equilibrating tautomers in aqueous solution. The change is attributed to the disorder of the aqueous environment. These are simple counterexamples to the hope that the crystal structure reveals the actual molecular structure in aqueous solution.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Structures of Active Site Histidine Mutants of IIIGlc, a Major Signal-transducing Protein in Escherichia coli. EFFECTS ON THE MECHANISMS OF REGULATION AND PHOSPHORYL TRANSFER.
J. G. Pelton, D. A. Torchia, S. J. Remington, K. P. Murphy, N. D. Meadow, and S. Roseman (1996)
J. Biol. Chem. 271, 33446-33456
   Abstract »    Full Text »    PDF »
Energy considerations show that low-barrier hydrogen bonds do not offer a catalytic advantage over ordinary hydrogen bonds.
A. Warshel and A. Papazyan (1996)
PNAS 93, 13665-13670
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