## Abstract The barriers to internal rotation about the CN bond in several thiopiperidides have been determined by the NMR technique. It was found that the barrier height (Δ__G__^‡^) increases in the series cinnamoylthiopiperididem‐and __p__‐substituted cinnamoylthiopiperidides the barriers were s
Restricted rotation in sterically hindered dichalcogenides. A dynamic NMR study
✍ Scribed by B. Mario Pinto; Ronald Y. N. Leung; R. Dev Sharma
- Publisher
- John Wiley and Sons
- Year
- 1988
- Tongue
- English
- Weight
- 573 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The rotational barriers in bis(2,4,Ctri-tert-butylphenyl) diselenide and ditelluride have been investigated by total line-shape analysis of variabletemperature 'H NMR spectra in CFCI,-CD,CI, (85: 15). The free energies of activation, AGf,,, K, for the diselenide and ditelluride were determined to be 49.4 & 0.6 and 39.2 f 0.2 kJ mol-', respectively. The difference is attributed to the dominance of steric effects in the transition state for rotation.
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## Abstract Free energies of activation, Δ__G__, for the rotation of the phenyl group in the range of 46.06–63.25 kJ mol^−1^ were observed in some model β‐hydroxyphosphonates. These barriers were found to depend on the type of substituents at the phosphorus atom and on the substituents at the β‐pos
Rates of rotations about the C-N' partial double bond in a series of six N',N' penta-and six N',N'-hexa-methylene-Nz-substituted-phenyformamidines were determined from 13C DNMR line shape analysis. Electron accepting substituents at the phenyl ring increase the barrier to rotation, and electron don
## Abstract The energy barriers associated with NO rotation in a series of __p__‐nitrosoanilines were measured by the total bandshape NMR method. Energies [Δ__G__^‡^ (298.15 K)] are in the range 38–57 kJ mol^−1^, the magnitudes being lowered appreciably by the presence of methyl substituents flank