Conformational Self-Poisoning in Crystal Growth

With the ever-increasing complexity of new drug compounds, their crystallization is becoming more challenging than ever. Controlling the crystallization of present and future drugs will remain a chimera unless we gain an improved understanding of the effects of molecular flexibility on crystal nucleation and growth at the molecular level. As a contribution to this understanding, we report here the growth kinetics of a series of diacids with chain lengths from 4 to 10 carbon atoms. These compounds are ideal for such a study since (a) they all crystallize as linear conformers, (b) their crystal structures are very similar across the series, and (c) their molecular flexibility increases with increasing chain length. Upon analysis of their crystal growth behavior, we stumbled upon a surprising finding: the growth of these crystals along the length increases linearly for the series up to the diacid containing seven carbon atoms, beyond which the rates drop dramatically. Such a dramatic decrease in growth rates at longer chain lengths cannot be explained by the crystal structure differences of the diacids. To gain further insights, we explored the conformational landscapes of two diacids in solution using well-tempered metadynamics simulations. With increasing chain length, the conformational landscape becomes more complex, with folded conformations becoming more important for long chain acids. Our simulations show that some of the minor conformers present in the solution act as potent crystal growth inhibitors (a phenomenon we refer to as conformational self-poisoning). To the best of our knowledge, this work represents the first report of conformational self-poisoning in crystal growth, with experimental evidence supported by a molecular-level mechanism. While this effect is bad news for crystallization scientists, who must work with complex flexible compounds, for these diacids, we show that selected solvents are able to disfavor the problematic conformers in the solution, turning off the self-poisoning effect.

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Publication Details

Journal
JACS Au
Published
2025-03-18
DOI
https://doi.org/10.1021/jacsau.5c00043
Citations
3
Primary Topic
Crystallization and Solubility Studies
Type
article
Field-Weighted Citation Impact
1.55

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article

Conformational Self-Poisoning in Crystal Growth

Roger J. Davey, Matteo Salvalaglio, Aurora J. Cruz‐Cabeza, Veselina Marinova et al.
3 citations
JACS Au
Crystallization and Solubility Studies
1.55
article

Conformational Self-Poisoning in Crystal Growth

Roger J. Davey, Matteo Salvalaglio, Aurora J. Cruz‐Cabeza, Veselina Marinova, Benjamin P. A. Gabriele, Yumin Liu
article en
3 citations

Abstract

With the ever-increasing complexity of new drug compounds, their crystallization is becoming more challenging than ever. Controlling the crystallization of present and future drugs will remain a chimera unless we gain an improved understanding of the effects of molecular flexibility on crystal nucleation and growth at the molecular level. As a contribution to this understanding, we report here the growth kinetics of a series of diacids with chain lengths from 4 to 10 carbon atoms. These compounds are ideal for such a study since (a) they all crystallize as linear conformers, (b) their crystal structures are very similar across the series, and (c) their molecular flexibility increases with increasing chain length. Upon analysis of their crystal growth behavior, we stumbled upon a surprising finding: the growth of these crystals along the length increases linearly for the series up to the diacid containing seven carbon atoms, beyond which the rates drop dramatically. Such a dramatic decrease in growth rates at longer chain lengths cannot be explained by the crystal structure differences of the diacids. To gain further insights, we explored the conformational landscapes of two diacids in solution using well-tempered metadynamics simulations. With increasing chain length, the conformational landscape becomes more complex, with folded conformations becoming more important for long chain acids. Our simulations show that some of the minor conformers present in the solution act as potent crystal growth inhibitors (a phenomenon we refer to as conformational self-poisoning). To the best of our knowledge, this work represents the first report of conformational self-poisoning in crystal growth, with experimental evidence supported by a molecular-level mechanism. While this effect is bad news for crystallization scientists, who must work with complex flexible compounds, for these diacids, we show that selected solvents are able to disfavor the problematic conformers in the solution, turning off the self-poisoning effect.

JACS AuVol. 5(4)
Durham University (GB), Chinese Academy of Sciences (CN), University of Manchester (GB), Thomas Young Centre (GB), Beijing National Laboratory for Molecular Sciences (CN), Institute of Chemistry (CN), University College London (GB)
Pfizer, Royal Society, China Scholarship Council, Syngenta International, Engineering and Physical Sciences Research Council
Zero hunger
Openalex Percentile: Top 19%
Crystallization and Solubility Studies
1.55
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