Nitrogen-15 NMR spectra of the complexes and ] , each containing 15N at natural abundance, were obtained by indirect detection (HMQC) using phosphorus as the observed nucleus. Data collection times varied from 4 h to 4 d depending upon the accuracy of the estimated value of 2J(31P,15N) used to opti
Characterization of two series of nitrogen-containing dendrimers by natural abundance 15N NMR
✍ Scribed by Rodolphe Deloncle; Yannick Coppel; Cyrille Rebout; Jean-Pierre Majoral; Anne-Marie Caminade
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 191 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2203
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Two series of small generation dendrimers built with phosphorus atoms at each branching point and various types of nitrogen atoms at natural abundance of ^15^N within the branches are characterized by a gradient enhanced GHNMQC (gradient hydrogen–nitrogen multiple quantum coherence) ^1^H^15^N NMR technique. The first series contains two types of nitrogen atoms, included in phosphorhydrazone linkages (CHNNMeP(S)), whereas the second series contains four types of nitrogen atoms included in azobenzene linkages (ArNNAr′) in addition to the phosphorhydrazone. The influence of the trans/cis isomerization of the azo bond on the ^15^N NMR has also been studied. Despite the low solubility of the azobenzene‐containing dendrimers, which renders the detection of some signals difficult, ^15^N NMR appears as a very sensitive tool to detect chemical changes in the dendritic structure. Copyright © 2008 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
A method is described for unequivocally establishing the site of N-oxidation which relies on the relatively large downÐeld shift of aliphatic nitrogen resonances following oxidation. The technique described is based on 15N at natural abundance and does not require labelling. 15N chemical shifts are
## Abstract Synthetic efforts towards the indole alkaloid natural product roquefortine C resulted in the formation of an unknown intermediate. Elucidation of the structure of this molecule relied on the use of long‐range ^1^H‐^15^N 2D‐NMR. Computational predictions were used to facilitate the locat