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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.


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