PCls is added portionwise with vigorous stirring to liquid NH3 at -70 'C. An almost clear solution is obtained which yields a white powder when the NH3 is evaporated off. The weight of the final precipitate reveals that 8 moles of NH3 have been taken up for each mole of PCI5. The product is kept at
Magnetic non-equivalence of methylene group protons in 1,2-disubstituted ferrocenes
β Scribed by G. Marr; R.E. Moore; B.W. Rockett
- Publisher
- Elsevier Science
- Year
- 1968
- Tongue
- French
- Weight
- 184 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Continued interest in the origin of the magnetic non-equivalence of protons in methylene groups attached to asymmetric centres (1) prompts us tc report our results with some 1,2disubstituted ferrocenes.
Several factors, including molecular asymmetry (2)) 2-substituent asymmetry (3), unequal conformer populations resulting from steric hindrance (lc, 4), and solvent (la) and temperature effects (3) may contribute to the observed chemical shift differences between the methylene group protons.
π SIMILAR VOLUMES
At room temperature in deuterochloroform solution, ethyl 2-(2,&dinitrophenyl) acetoacetate exists in the enol form, as shown\* by a one proton singlet at 13.18 6 in the proton magnetic resonance (p.m.r.) -1 spectrum (l), and the absence of any strong 3 C-0 band above l'i'O0 cm in the infra-red. The
The magnetic equivalence or non-equivalence of the methylene hydrogens of a benzyl group has proven to be an effective probe for chirality in a substrate.' An AB quartet for the nmr resonance signal of the aliphatic protons of a single benzyl substituent is positive evidence for chirality( in the sy
## Abstract Examples are given of the conformationally dependent influence of 3βsubstituents (methyl, __n__βpropyl, allyl, aryl, hydroxy and acyloxy) on the magnetic nonβequivalence of the benzylic methylene protons (N__CH__~2~Ph) of __N__βbenzylpiperidine as observable by ^1^H NMR. The results, to