## Abstract Multinuclear magnetic resonance studies (^1^H, ^13^C, ^15^N, ^31^P) of three phosphorus–nitrogen compounds [__tert__‐butylamino‐__tert__‐butylfluorophosphane (1), __tert__‐butylimino‐__tert__‐butylphosphane (2) and its dimer (3)], in which numerous one‐ and two‐dimensional NMR experimen
13C, 15N and 31P NMR Investigation of P-Substituted N-2,4,6-Tris(tert-butyl)- phenyliminophosphines
✍ Scribed by A. B. Rozhenko; M. I. Povolotskii; V. V. Polovinko
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 507 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
A large series of (Qand (a-iminophosphines, Mes*-N=P-X [X = NR,, OR, Alk, Ar, SR, PR,, Hal; Mes* = 2,4,6-tris(tert-butyI)phenyl], was investigated by 13C, I5N and 31P NMR spectroscopy. The 13C NMR chemical shifts of methyl groups of the o-tert-butyl substituents, and also the carbon-phosphorus coupling of the meta-and para-carbons in the aromatic moiety, were shown to be possible criteria for the assignment of the Eor 2-configuration of the iminophosphine. Basic rules are enumerated for the determination of configuration in the series considered. The variation of aromatic I3C nuclei shielding is considered to be electrostatic (n-inductive) in nature.
📜 SIMILAR VOLUMES
The iniluence of substituents on the 'H, "C and 15N NMR chemical shifts of 2-substituted 5(6)nitrobenzimidazoles and their analogues labelled with 15N in the nitro group was investigated. It was found that the substituent effects are transmitted to the carbon and hydrogen nuclei in positions 4-7 mai