## Abstract The preferred conformation of aminophosphanes with bulky amino groups (**__1–20__**) was determined by NMR spectroscopy in solution, in two cases in the solid state (**__11,17__**) and in one case (**__11__**) by X‐ray crystallography. Trimethylsilylaminodiphenylphosphanes Ph~2~PN(R)SiM
Aminodiphenylphosphanes: Isotope-induced chemical shifts 1Δ14/15N(31P), coupling constants 1J(31P,15N), and chemical shifts δ15N and δ31P
✍ Scribed by Rosalinda Contreras; Jean Michel Grevy; Zureima García-Hernández; Marisol Göizado-Rodriguez; Bernd Wrackmeyer
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 244 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1042-7163
- DOI
- 10.1002/hc.1083
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✦ Synopsis
The isotope-induced chemical shifts 1 14/15 N( 31 P) were determined at natural abundance of 15 N by using HEED INEPT experiments. A dependence of 1 14/15 N( 31 P) on the substituents at nitrogen was found (alkyl < H < aryl; increasingly negative values). The magnitude and sign of the coupling constants 1 J( 31 P, 15 N) (positive sign
📜 SIMILAR VOLUMES
N-Triorganostannyl pyrroles (1) and indoles (2) [R \ Me (a), Et (b), tBu (c)], N-(R Sn)-substituted trimethylstannyl-carbazole (3), N-trimethylstannyl-2,5-dimethylpyrrole (1d), the corresponding silicon and lead derivatives [1d(Si) and 1d(Pb)] and N-trimethylstannyl-2-methylindole (2d) were prepare
2-Aminopyridines (l), 2-amino-3-methylpyridines (2) and 2,6-diaminopyridines (3), bearing N-trimethylsilyl, -stannyl or -plumby1 groups, and analogously substituted 2-picolines (4) were studied by 'H, 13C, "N, 29Si, '19Sn and ' O' Pb NMR spectroscopy. Intramolecular N S n coordination became evident