𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Quantitative 15N NMR spectroscopy

✍ 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

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Line intensities in ^15^N NMR spectra are strongly influenced by spin‐lattice and spin–spin 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 nitrogen‐containing 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.


πŸ“œ SIMILAR VOLUMES


NMR spectroscopy quantitation
✍ Paul Van Hecke; Sabine Van Huffel πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 27 KB
15N NMR spectroscopy of some azines
✍ L. Stefaniak; John D. Roberts; M. Witanowski; G. A. Webb πŸ“‚ Article πŸ“… 1984 πŸ› John Wiley and Sons 🌐 English βš– 451 KB
Characterization of biguanides by 15N NM
✍ B. Clement; U. Girreser πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 82 KB πŸ‘ 2 views

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

15N-NMR Spectroscopy, 15. The Structure
✍ Hull, William E. ;Kricheldorf, Hans R. πŸ“‚ Article πŸ“… 1980 πŸ› John Wiley and Sons 🌐 English βš– 398 KB πŸ‘ 1 views

## Abstract The natural abundance ^15^N‐NMR 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 four‐ring structure. ^13^C‐NMR data provide