Activation parameters have been determined in the gas phase for the geometrical isomerization of the double bonds in two phenyl-substituted methylenecyclopropanes (2 and 8). Comparison with the analogous values for three sterically non-restricted styrene derivatives (15, 16 and 17) shows that the e
A rotational barrier about the isopropyl to aryl bond in highly substituted sulphines
✍ Scribed by Albert Tangerman; Binne Zwanenburg
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 332 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The rotational barriers in sulphines containing the substituents 2,6‐dimethyl‐3‐isopropyl‐4‐methoxyphenyl and 4,6‐dimethyl‐3‐isopropyl‐2‐methoxyphenyl are discussed. Particular attention is given to the occurrence of a barrier to rotation about the isopropyl to aryl bond. In both types of sulphines the isopropyl group is flanked by a methyl and a methoxy group. The isopropyl to aryl barrier could only be detected in the sulphines containing the second type of substituent where the o‐methoxy group experiences a buttressing effect from the CSO moiety.
📜 SIMILAR VOLUMES
## Abstract The ^19^F NMR spectra of mono‐ and difluoroacetamide are used to derive the activation parameters for rotation about the CN bond; it is not possible to obtain useful results for trifluoroacetamide. A total line shape analysis is used. Unusually large deuterium isotope effects upon the
## Abstract For Abstract see ChemInform Abstract in Full Text.