Chiral Amplification through the Interplay of Racemizing Conditions and Asymmetric Crystal Growth

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DOI http://dx.doi.org/10.1021/jacs.2c10584
Reference S.W. van Dongen, I. Ahlal, M. Leeman, B. Kaptein, R.M. Kellogg, I. Baglai and W.L. Noorduin, Chiral Amplification through the Interplay of Racemizing Conditions and Asymmetric Crystal Growth, J. Am. Chem. Soc. 145, (1), 436-442 (2023)
Group Self-Organizing Matter

Amplification of enantiomeric excesses (ee) is routinely observed during chiral crystallization of conglomerate crystals for which the enantiomers undergo racemization in solution. Although routes comprising a combination of crystal growth and dissolution are frequently used to obtain enantiopure molecules, crystal growth by itself has rather been considered as a source of enantiomeric erosion and discounted as a potential source of enantiomeric amplification. Counterintuitively, we here demonstrate striking enantiomeric amplification during crystal growth for clopidogrel and tert-leucine precursors. Based on a mechanistic framework, we identify that the interplay between racemization and crystal growth rates elicits this surprising effect. The asymmetric amplification of the solid-phase ee can be enhanced by increasing the mass of grown material relative to the product such that small amounts of seeds of only 60% ee already result in virtually exclusive growth of the majority phase. These results impact our understanding of asymmetric amplification mechanisms during crystallization and offer a tangible basis for practical production of enantiopure molecules.