Are there single-well hydrogen bonds in pyridine-dichloroacetic acid complexes?
The (18)O-induced isotope shifts in (13)C NMR spectra of 1:1 complexes of Cl(2)CHC(18)O(2)H with a series of substituted pyridines in CD(2)Cl(2) at low temperature reach a maximum when the acidities of the hydrogen-bond donors are matched, consistent with a mixture of tautomers, and with no drop tha...
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2010-01, Vol.46 (3), p.481-483 |
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| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | The (18)O-induced isotope shifts in (13)C NMR spectra of 1:1 complexes of Cl(2)CHC(18)O(2)H with a series of substituted pyridines in CD(2)Cl(2) at low temperature reach a maximum when the acidities of the hydrogen-bond donors are matched, consistent with a mixture of tautomers, and with no drop that would indicate a single-well H-bond. |
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| ISSN: | 1359-7345 1364-548X |
| DOI: | 10.1039/b917765e |