Abstract
In an earlier study, we obtained experimental evidence of the oscillatory transenantiomerization of selected profen drugs (e.g., S-(+)-ibuprofen, S-(+)-naproxen, and S-(+) and R-(−)-flurbiprofen) dissolved in aqueous, aqueous-organic, and purely organic liquid media. This process was apparently catalyzed by basic or amphiprotic environments and involved keto-enol tautomerism, and the self-organization of molecules in the solution via association of the carboxylic functional group of profens through hydrogen bonding to form mixed H-bonded associates with the remaining constituents of the solution. A model of the oscillatory transenantiomerization of profens was also developed by adapting an earlier oscillatory model, the Templator. Our new model comprises two linked Templators. The essence of the Templator model adapted to the oscillatory transenantiomerization of profens is the assumption that the H-bonded profen homodimer acts as a template, able to generate new dimers having the same steric configuration as their respective monomeric units.
As profens belong to the class of 2-arylpropionic acids (2-APAs), we concluded that the phenomenon of oscillatory transenantiomerization may occur in other 2-APAs as well, among them those amino acids whose molecular structure can formally be derived from propionic acid. Thus, in this study, we focus our attention on L-α-phenylalanine (LPA; one of the nine amino acids essential for humans). Using thin layer chromatography (TLC) and polarimetry, we demonstrate the ability of LPA to undergo oscillatory transenantiomerization analogous to that observed with profens. The self-organization of molecules in a 70% ethanol solution of LPA is confirmed with photographs taken in UV light (λ = 254 nm). Finally, we propose a skeleton molecular mechanism for the transenantiomerization of LPA and simulate the oscillatory interconversion of its L and D forms with two linked Templators.
ACKNOWLEDGMENT
The authors thank Merck KGaA (Darmstadt, Germany) for supplying the TLC plates used in our experiments. This work was supported in part by the U.S. National Science Foundation (grant CHE-0615507).