期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 20, 期 35, 页码 11058-11068出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201402858
关键词
fluorine; NMR spectroscopy; hydrogen bonds; molecular electrostatic potential; noncovalent interactions
Hydrogen-bonding interactions play an important role in many chemical and biological systems. Fluorine acting as a hydrogen-bond acceptor in intermolecular and intramolecular interactions has been the subject of many controversial discussions and there are different opinions about it. Recently, we have proposed a correlation between the propensity of fluorine to be involved in hydrogen bonds and its F-19 NMR chemical shift. We now provide additional experimental and computational evidence for this correlation. The strength of hydrogen-bond complexes involving the fluorine moieties CH2F, CHF2, and CF3 was measured and characterized in simple systems by using established and novel NMR methods and compared to the known hydrogenbond complex formed between acetophenone and p-fluorophenol. Implications of these results for F-19 NMR screening are analyzed in detail. Computed values of the molecular electrostatic potential at the different fluorine atoms and the analysis of the electron density topology at bond critical points correlate well with the NMR results.
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