## Carbon -13 relaxation times, Tl, have been measured for ten cobalt(III)-cyclohexanedione dioxime complexes: CH,CH,-Co(Niox),-pR-pyridine [R = H, N(CH,),, CH,, C,H,, C(CH,),, Cl, Br, CN and COCH,] and CH,CH,-Co(Niox),-3-N-methylimidazole. The values obtained have been rationalized by making assu
Structural studies of metalloporphyrins. VI—13C relaxation time, T1, measurements and the nature of the axial N—metal bond in some macrocyclic complexes
✍ Scribed by J. Huet; A. Gaudemer
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- English
- Weight
- 574 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Rotation barriers around the metal—pyridine bond of various macrocyclic complexes of cobalt(III), rhodium(III), zinc(II) and magnesium(II) have been studied using the ^13^C longitudinal relaxation times, T~1~, of the carbon atoms of pyridine and the macrocycle. The data have been rationalized on the basis of steric and electronic factors. The influence of π back‐donation on the rates of rotation around the axial CoN and RhN bonds is discussed. The agreement found between the conclusions drawn from this study and X‐ray data reported for complexes of identical or closely related structure demonstrates the validity of this method.
📜 SIMILAR VOLUMES