Wikipedia

Enantiomer self-disproportionation

Enantiomer self-disproportionation is a process in stereochemistry describing the separation of a non-racemic mixture of enantiomers in an enantioenriched fraction and a more racemic fraction as a result of the formation of heterochiral or homochiral aggregates. This process is known to occur in achiral column chromatography.

The phenomenon was first reported in 1983[1] in the separation of an excess of carbon-14 labeled (S)-(−)-nicotine enantiomer and its isomer. Two fractions were recorded, one containing racemic nicotine and the other pure (S) enantiomer.

In 2006, Vadim A. Soloshonok[2] introduced the term Enantiomer self-disproportionation or self-disproportionation of enantiomers. He investigated achiral separations of several trifluoromethyl compounds.

Enantiomer self-disproportionation (S)-trifluoromethyl substrate

By column chromatography on regular silica gel with a hexane / ethyl acetate eluent (5:1), a 66.6% ee sample of a trifluoromethyl substrate is separated into several fractions ranging from 8.1% ee for the first fraction collected to > 99.9% ee for the last fraction collected. A presence of a strong electronegative group in the substrate such as the trifluoromethyl group is a prerequisite. The effect disappears when a more polar eluent is selected. A possible explanation is offered. Compounds with large electronegative groups such as trifluoromethyl can form supramolecular associations or aggregates or clusters in which these groups are separated from each other as much as possible with minimized electrostatic repulsions. When these associations are stacks of alternating (R) and (S) molecules (as in syndiotactic polymers) this can be accomplished very efficiently. This association will form a racemic fraction of relatively high molecular weight eluting more slowly than the non-associating enantiopure fraction.

See also

References

  1. ^ Unexpected phenomenon in the high-performance liquid chromatographic analysis of racemic 14C-labelled nicotine: Separation of enantiomers in a totally achiral system K. C. Cundy, P. A. Crooks, J. Chromatogr. 1983, 281, 17. Abstract
  2. ^ Remarkable Amplification of the Self-Disproportionation of Enantiomers on Achiral-Phase Chromatography Columns Vadim A. Soloshonok Angewandte Chemie International Edition Volume 45, Issue 5, Pages 766 - 769 2006 Abstract
This article is copied from an article on Wikipedia® - the free encyclopedia created and edited by its online user community. The text was not checked or edited by anyone on our staff. Although the vast majority of Wikipedia® encyclopedia articles provide accurate and timely information, please do not assume the accuracy of any particular article. This article is distributed under the terms of GNU Free Documentation License.

Copyright © 2003-2025 Farlex, Inc Disclaimer
All content on this website, including dictionary, thesaurus, literature, geography, and other reference data is for informational purposes only. This information should not be considered complete, up to date, and is not intended to be used in place of a visit, consultation, or advice of a legal, medical, or any other professional.