## Abstract A series of ten (__E__)‐stilben‐4‐ols, HOPhCHCHPhX, with X = H, 4′‐Cl, 4′‐F, 4′‐Me, 4′;‐OMe, 3′‐Me, 3′‐OMe, 3′‐OH, 3′‐F and 3′,4‐diOMe, were studied using one‐ and two‐dimensional NMR techniques. Interpretation of these spectra led to definitive assignments of all carbon and hydrogen c
13C- and 1H-NMR. Studies on the Configuration of Tricarbonyliron Complexes of Oxa- and Aza[4.4.3]propellanes
✍ Scribed by Kurt Bachmann; Wolfgang Von Philipsborn; Chaim Amith; David Ginsburg
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 530 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The configurations of a series of mono‐ and bis‐Fe(CO)~3~ complexes of 12‐oxa[4.4.3]‐propella‐2,4,7,9‐tetraene (1) and of 11,13‐dioxo‐12‐methyl‐12‐aza[4.4.3]propella‐2,4,7,9‐tetraene (7) as well as of a trienic aza‐propellane complex have been studied in solution by ~13~C‐ and ~1~H‐NMR. spectroscopy. Praseodymium‐induced ~13~C‐shifts of the metalcarbonyl carbon atoms and of the central carbon atom of the complexed diene systems are particularly sensitive and useful to prove exo‐ or endo‐configuration of the tricarbonyliron ligand. In addition, H,H‐ and C,H‐coupling constants of the complexes and parent compounds are reported and discussed.
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