Intermolecular hydrogen-bonding effects on13C NMR shielding for enol forms of diketones in the solid state
β Scribed by F. Imashiro; S. Maeda; K. Takegoshi; T. Terao; A. Saika
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- English
- Weight
- 225 KB
- Volume
- 92
- Category
- Article
- ISSN
- 0009-2614
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β¦ Synopsis
From high-resolution solid-state lSC NMR spectra for the enol forms of some diketones, an average chemical shift of the carbonyl and enol carbons in dimedone is found to move remarkably downfield compared with the corresponding shift in DMSO~/6, which is ascribed to a strong intermolecular hydrogen bond in the solid state.
π SIMILAR VOLUMES
The inΓuence of hydrogen bonding (HB) on the 13C chemical shift tensors in four solid amino acids was studied by the ab initio gauge-included atomic orbital (GIAO) approach. The results of the present calculations were compared with those predicted previously and with the experimentally observed shi
In high-resolution solidstate CP/MAS 13C NhfR spectra of several hydrosybenzaldehydes, the downfield shifts due to hydrogen bonding for the carbonyl carbons are found to vary inversely with the O...O hydrogen-bond distances\_ Conformations of the aldehyde groups in the solid state are determined by