## Abstract The ^13^C‐NMR. in Zn(II) (Protoporphyrin IX), Fe(III) (Protoporphrin IX) (CN)~2~, Zn(II) (Deuteroporphyrin IX dimethylester), and Fe(III) (Deuteroporphyrin IX) (CN)~2~ have been identified, and the ^13^C hyperfine shifts in the iron complexes evaluated. In a partial analysis of these da
Hyperfine Shifts of the 13C-NMR. in low spin iron(III) porphyrin complexes
✍ Scribed by Kurt Wüthrich; Rudolf Baumann
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- German
- Weight
- 676 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Abstract
The ^13^C‐NMR. in Zn(II)(Porphin), Fe(III)(Porphin)(CN~2~), Zn(II)(Tetraphenyl‐porphin), and Fe(III)(Tetraphenylporphin)(CN~2~) have been identified, and the ^13^C hyperfine shifts in the iron complexes evaluated. It was found that dipole‐dipole coupling with the electron spin localized in the π‐orbitals of the aromatic carbon atoms makes an important contribution, to the ^13^C hyperfine shifts. In a preliminary analysis the experimental spin density distribution obtained from the combined ^1^H‐ and ^13^C‐NMR.‐data is compared with theoretical models of the iron porphyrin complexes.
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