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 cou
13C NMR and ESR spectroscopic investigations on tert-butyl-substituted cyclopentadienones
✍ Scribed by Hans-Otto Kalinowski; Lothar H. Franz; Günther Maier
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 383 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
^13^C NMR spectra of 11 di‐, tri‐ and tetra‐tert‐butyl‐substituted cyclopentadienones are discussed with respect to charge distribution and substituent effects. The chemical shifts of the unsubstituted cyclopentadienone, calculated from substituent increments, are in good agreement with published CNDO calculations and can be rationalized by the inductive effect of the carbonyl group. In addition, the ESR signals shown by some of the cyclopentadienones are described, and possible reasons for their appearance are discussed.
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