**Study of the Photochemical Behaviour of Some Diaryl‐1,3‐triazenes** The photolysis of Diaryl‐1,3‐triazenes gives products whose structures are consistent with a cage recombination process of homolytically formed radicals and subsequent abstraction of hydrogen from the solvent molecules by arylami
Triazènes. Etude XPS. et 1H-RMN. des complexes mercuriques des diaryl-1,3-triazènes
✍ Scribed by Jean-Claude Maire; André Baldy; Daniel Boyer; Pierre Llopiz; Gaston Vernin; Beni Prashad Bachlas
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- German
- Weight
- 190 KB
- Volume
- 62
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
XPS. and ^1^H‐NMR. spectra of 1,3‐diaryltriazenes complexes of Hg(II)
The core binding energies C 1__s__, N 1__s__, Hg 4__f__~7/2~, Hg 4__f__~5/2~ in 7 symmetrical p‐substituted 1,3‐diphenyltriazenes complexes of Hg(II) have been measured by XPS. Within the limits of experimental error (± 0.2 eV) only one N 1__s__ signal could be detected. This indicates the equivalence of the 3 N‐atoms. Invariance of C 1__s__, N 1__s__, Hg 4__f__~7/2~, Hg 4__d__~5/2~ signals with the para substituents on the phenyl ring is explained on the basis of ionic character in the Hg, N bond. These results are corroborated by the ^1^H‐NMR. spectra.
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