Parallel alignment of electric and magnetic transition dipole moments in chiral additives can boost the oxygen evolution reaction

Homochirality, the uniformity in single molecular handedness, is a defining feature of life. Although universal in biology, the evolutionary advantage of selecting one enantiomer over its mirror image remains unresolved. One possible clue may lie in catalysis itself: recent studies demonstrate that oxygen evolution reaction (OER), a key step in photosynthesis, is sensitive to chirality. Here, we report that electrochemical OER performance with chiral additives may be correlated to the alignment of their electric (ETDM) and magnetic (MTDM) transition dipole moments in the lowest-energy transition. Enantiomers with parallel ETDM-MTDM configurations consistently outperform their antiparallel counterparts. Notably, this bias also manifests in natural systems, suggesting a shared stereoelectronic principle. We define this stereoelectronic correlation as the Supplementary Angle Effect (SAE). Our findings establish SAE in electrocatalysis offering a quantitative descriptor for assessing how molecular handedness affects catalytic behavior and enantiodifferential performance.

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Publication Details

Journal
Communications Chemistry
Published
2026-04-27
DOI
https://doi.org/10.1038/s42004-026-02042-2
Primary Topic
Origins and Evolution of Life
Type
article
Field-Weighted Citation Impact
0.00

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article

Parallel alignment of electric and magnetic transition dipole moments in chiral additives can boost the oxygen evolution reaction

Isilda Amorim, Joonas Uusitalo, Laura M. Salonen, Ani Ozcelik et al.
Communications Chemistry
Origins and Evolution of Life
article

Parallel alignment of electric and magnetic transition dipole moments in chiral additives can boost the oxygen evolution reaction

Isilda Amorim, Joonas Uusitalo, Laura M. Salonen, Ani Ozcelik, Fabrizio Santoro, Ángeles Peña‐Gallego, José Lorenzo Alonso‐Gómez, S. Chiussi, Yury V. Kolen’ko, Daniel Aranda, Julia Portela‐Pino
article en

Abstract

Homochirality, the uniformity in single molecular handedness, is a defining feature of life. Although universal in biology, the evolutionary advantage of selecting one enantiomer over its mirror image remains unresolved. One possible clue may lie in catalysis itself: recent studies demonstrate that oxygen evolution reaction (OER), a key step in photosynthesis, is sensitive to chirality. Here, we report that electrochemical OER performance with chiral additives may be correlated to the alignment of their electric (ETDM) and magnetic (MTDM) transition dipole moments in the lowest-energy transition. Enantiomers with parallel ETDM-MTDM configurations consistently outperform their antiparallel counterparts. Notably, this bias also manifests in natural systems, suggesting a shared stereoelectronic principle. We define this stereoelectronic correlation as the Supplementary Angle Effect (SAE). Our findings establish SAE in electrocatalysis offering a quantitative descriptor for assessing how molecular handedness affects catalytic behavior and enantiodifferential performance.

Communications Chemistry
University of Helsinki (FI), Institute for the Chemistry of OrganoMetallic Compounds (IT), Finnish Museum of Natural History (FI), International Iberian Nanotechnology Laboratory (PT), Universidade de Vigo (ES), Universidad de Málaga (ES)
Ministerio de Ciencia, Innovación y Universidades, Ministerio de Ciencia e Innovación, Universidade de Vigo, Xunta de Galicia, Agencia Estatal de Investigación, European Social Fund
Openalex Percentile: Top 6%
Origins and Evolution of Life
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