## Abstract Data on ^13^C chemical shifts and ^13^C^1^H spin coupling constants of norbornane (**1**), norbornene (**2**), norbornadiene (**3**), benzonorbornene (**4**) and benzonorbornadiene (**6**) are reported. The non‐equivalence in __J__(^13^CH) values determined from the two bridge methyle
An 1H and 13C NMR study of pentane-2,4-dione tellurium(II) compounds; chemical shifts, 125Te1H and 125Te13C couplings
✍ Scribed by John C. Dewan; W. Brian Jennings; Jack Silver; Malcolm S. Tolley
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 362 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
^1^H and ^13^C NMR data are reported for pentane‐2,4‐dione tellurium(II) compounds which contain a 6‐membered tellurane ring bearing methyl or ethyl substituents. The ^125^TeCH coupling constants are particularly interesting in that they are highly stereospecific, viz. ∼60 Hz and 0–8 Hz for equatorial and axial protons, respectively, in the chair conformation. ^1^J(TeC) and ^2^J(TeCC) couplings lie in the ranges 118–146 Hz and 44–49 Hz, respectively. Geminal HCH couplings in these compounds (9–11 Hz) are lower than analogous values in tellurane or in cyclohexane‐1,3‐diones.
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