Studies of line width and chemical shift us. temperature for amide and hydroxyl proton magnetic resonance signals from: barbituric acid, dialuric acid, parabanic acid, alloxan and alloxan monohydrate dissolved in anhydrous dimethyl sulfoxide-d6 are reported. The behavior of the amide signals shows t
Differences of proton tautomerism in substituted porphyrins
✍ Scribed by L. Kümmerl; H. Kliesch; D. Wöhrle; D. Haarer
- Book ID
- 103031112
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 556 KB
- Volume
- 227
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
The stability of the photochemical hole-burning process due to a back reaction of the inner protons of porphyrins is investigated as a function of various substituents of the porphyrin skeleton. For that purpose thermal cycling experiments were performed and the dynamics of the observed spectral changes were measured at different temperatures on a timescale of minutes. The four porphyrins which were investigated exhibit in the range from 90 to 170 K rather large differences in the mean rates describing the tautomerization reactions. We attribute these differences to sterical distortions of the porphyrin ring and to the different electronic properties of the involved sidegroups.
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