Quantitative 15N NMR spectroscopy
β Scribed by George C. Levy; T. Pehk; P. R. Srinivasan
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 410 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Abstract
Line intensities in ^15^N NMR spectra are strongly influenced by spinβlattice and spinβspin relaxation times, relaxation mechanisms and experimental conditions. Special care has to be taken in using ^15^N spectra for quantitative purposes. Quantitative aspects are discussed for the ^15^N NMR of molecules with different nitrogen functional groups and also mixtures of nitrogenβcontaining compounds. It is shown that, in general, quantitative data are obtainable from integration of ^15^N lines in proton decoupled ^15^N NMR spectra using NOE suppression. Addition of paramagnetic relaxation reagents (PARR) under controlled conditions is frequently needed to accomplish the experiment within reasonable time limits.
π SIMILAR VOLUMES
The monoprotonated biguanides phenformin hydrochloride, buformin hydrochloride and metformin hydrochloride were investigated by 15 N NMR spectroscopy. The structure of all hydrochlorides is best described by a 1,3-diazabutadienic skeleton with three amino groups and its corresponding mesomeric forms
## Abstract The natural abundance ^15^NβNMR spectra of streptomycin and dihydrostreptomycin in aqueous solution at pH 5 show conclusively that the aldehyde group of streptomycin does not react with the methylamino or guanidino groups internally to form a fourβring structure. ^13^CβNMR data provide