Phosphorus–nitrogen rotation barriers: Further studies
✍ Scribed by S. Distefano; H. Goldwhite; E. Mazzola
- Book ID
- 102528213
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 394 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Phosphorus–nitrogen rotation barriers have been determined by low temperature NMR methods in a variety of compounds of the type RP(X)NR~2~′. The observed activation parameters are concentration and solvent independent. Increasing the bulk of substituents on nitrogen increases the barrier. Phosphonamidous fluorides (X = F) have lower barriers than the corresponding chlorides (X = Cl). Increasing the bulk of substituents on phosphorus decreases the barrier.
📜 SIMILAR VOLUMES
## Per-n Press.
The barrier to the internal rotation of the dirnethylamino group in thioamides of structure R-CS-N(CH,),, R being (CH,),N-CS--, CH,O,C-or N=C--, is studied by proton magnetic resonance, using the lineshape analysis method of Nakagawa. In the solvents o-dichlorobenzene, naphthalene and nitrobenzene a
A new type of alkylamines possessing high nitrogen inversion-rotation (NIR) barriers is described (in general, these are hindered cyclic amines). The increase in barrier values for these amines is caused by an increase in steric interactions in the NIR transition state due to restrictions for N-subs