Toward Unraveling Solvent-Induced Chirality at the Solid–Liquid Interface

Chiral induction by the solvent phase offers a promising route to achieve homochirality in self-assembled molecular networks. In this work, we examine solvent-driven chiral induction at the solid-liquid interface, where an enantiopure solvent biases the handedness of two-dimensional (2D) networks formed by achiral molecules physisorbed on the basal plane of highly oriented pyrolytic graphite. Using scanning tunneling microscopy at the liquid-solid interface, we visualize the 2D organization of the achiral monomer 10,12-pentacosadiynoic acid in chiral liquid environments. We compare the induction efficiencies of several enantiopure citronellyl-derived solvents that differ in their capacities for specific solute-solvent interactions. Complementary molecular dynamics simulations provide molecular-level insight into the possible mechanisms of solvent-mediated chiral induction.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2026-05-11
DOI
https://doi.org/10.1021/acs.jpclett.6c00753
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Toward Unraveling Solvent-Induced Chirality at the Solid–Liquid Interface

Andrea Minoia, Oleksandr Ivasenko, Lifeng Chi, Sven Bernaerts et al.
The Journal of Physical Chemistry Letters
Surface Chemistry and Catalysis
article

Toward Unraveling Solvent-Induced Chirality at the Solid–Liquid Interface

Andrea Minoia, Oleksandr Ivasenko, Lifeng Chi, Sven Bernaerts, Jie Zhang, Alexandre Mamontov, Yuan Fang, Yves H. Geerts, Steven De Feyter, C. Elizabeth Killalea, Roberto Lazzaroni, Kunal S. Mali
article en

Abstract

Chiral induction by the solvent phase offers a promising route to achieve homochirality in self-assembled molecular networks. In this work, we examine solvent-driven chiral induction at the solid-liquid interface, where an enantiopure solvent biases the handedness of two-dimensional (2D) networks formed by achiral molecules physisorbed on the basal plane of highly oriented pyrolytic graphite. Using scanning tunneling microscopy at the liquid-solid interface, we visualize the 2D organization of the achiral monomer 10,12-pentacosadiynoic acid in chiral liquid environments. We compare the induction efficiencies of several enantiopure citronellyl-derived solvents that differ in their capacities for specific solute-solvent interactions. Complementary molecular dynamics simulations provide molecular-level insight into the possible mechanisms of solvent-mediated chiral induction.

The Journal of Physical Chemistry Letters
University of Mons (BE), Université Libre de Bruxelles (BE), Soochow University (CN), International Solvay Institutes (BE), KU Leuven (BE)
Suzhou Key Laboratory of Functional Nano and Soft Materials, National Natural Science Foundation of China, Fonds De La Recherche Scientifique - FNRS, Fonds Wetenschappelijk Onderzoek, Suzhou Municipal Science and Technology Bureau, Collaborative Innovation Center of Suzhou Nano Science and Technology, Higher Education Discipline Innovation Project
Openalex Percentile: Top 9%
Surface Chemistry and Catalysis
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