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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

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✦ 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 CoN and RhN 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.


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13C relaxation times, T1, in six-coordin
✍ Jack Huet; A. Gaudemer 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 677 KB

## 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