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.
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 1297-1304 |
| Seitenumfang | 8 |
| Fachzeitschrift | Monatshefte fur Chemie |
| Jahrgang | 135 |
| Ausgabenummer | 10 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - Okt. 2004 |
| Extern publiziert | Ja |
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