Predicted NMR Coupling Constants Across Hydrogen Bonds: A Fingerprint for Specifying Hydrogen Bond Type?
- 25 March 2000
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (14) , 3560-3561
- https://doi.org/10.1021/ja994312h
Abstract
No abstract availableThis publication has 22 references indexed in Scilit:
- Understanding enzymic catalysis: the importance of short, strong hydrogen bondsChemistry & Biology, 1997
- Energy considerations show that low-barrier hydrogen bonds do not offer a catalytic advantage over ordinary hydrogen bondsProceedings of the National Academy of Sciences, 1996
- Electron correlation effects on the theoretical calculation of nuclear magnetic resonance spin–spin coupling constantsThe Journal of Chemical Physics, 1996
- Short strong hydrogen bonds: can they explain enzymic catalysis?Chemistry & Biology, 1996
- Structure and NMR Spectra of the 2-Norbornyl Carbocation: Prediction of 1J(13C13C) for the Bridged, Pentacoordinate Carbon AtomJournal of the American Chemical Society, 1996
- Predicted NMR Spectra for Ethyl Carbocations: A Fingerprint for Nonclassical Hydrogen-Bridged StructuresJournal of the American Chemical Society, 1995
- Coupled-cluster calculations of indirect nuclear coupling constants: The importance of non-Fermi contact contributionsThe Journal of Chemical Physics, 1994
- Low-Barrier Hydrogen Bonds and Enzymic CatalysisScience, 1994
- Electrostatic stabilization can explain the unexpected acidity of carbon acids in enzyme-catalyzed reactionsJournal of the American Chemical Society, 1993
- Low-barrier hydrogen bonds and low fractionation factor bases in enzymic reactionsBiochemistry, 1992