Abstract
Photodiastereomerization of urocanic acid and its human serum albumin complex (its binding constant was estimated to amount 4.1·10 -4dm3·mol-1) was investigated. It was found that although the photodiastereomerization rates were similar, the photoequilibrium positions differed significantly ((E):(Z) = 33:77 for free urocanic acid, and 50:50 for the complex). This is thought to be due to a different stabilization of the corresponding orthogonal excited states. The thermal barrier of diastereomerization was estimated to amount to more than 250 kJ·mol-1 making it a very unlikely process under physiological and photodiastereomerization conditions. The various prototropic species of the two diastereomers at various pH values were analyzed by means of a mathematical model and from these results a novel photoinduced pH-jump methodology allowing for fast, persistent, diffusion controlled, and bidirectional jumps is proposed.
| Original language | English |
|---|---|
| Pages (from-to) | 1297-1304 |
| Number of pages | 8 |
| Journal | Monatshefte fur Chemie |
| Volume | 135 |
| Issue number | 10 |
| DOIs | |
| Publication status | Published - Oct 2004 |
| Externally published | Yes |
Keywords
- Diastereomerization
- pH-Jump
- Photochemistry
- Protic equilibria
- Thermal stability