Spectroscopic studies on the protonation of Schiff bases
โ Scribed by R. De Bicca Alencastro; S. Badilescu; L. S. Lussier; C. Sandorfy; H. Le Thanh; D. Vocelle
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 469 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0020-7608
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โฆ Synopsis
Abstract
This short review concerns the protonation of Schiff bases by halogenic or carboxylic acids with a bias toward the chromophore of visual and bacterial rhodopsins. It is pointed out that the weak acids available in these pigments could not protonate the retinyl Schiff base 100% and that a supporting mechanism is needed to achieve full protonation. Our Fourier transform infrared studies both at room and low temperatures relating to this problem are summarized, and the propable role of water is emphasized.
๐ SIMILAR VOLUMES
The pyridoxal Schiff bases of the polypeptides poly(L-lysine), poly(L-ornithine), and poly(L-a,y-diaminobutyric acid) were prepared and investigated in water/methanol by CD spectra and equilibrium dialysis experiments. Only the poly(L-a,?-diaminobutyric acid) derivative is characterized by a relevan