ArticleNature communications2023
Inducing transient enantiomeric excess in a molecular quantum racemic mixture with microwave fields.
Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
3 citing papers in PubMed.
- Shaping light in 3D for direct asymmetric photochemistry: a 1000-fold enantioselectivity enhancement.Nature communications · 2026Article
- Enantiospecific two-photon electric-dipole selection rule of chiral molecules.Science advances · 2025Article
- Quantum Tunneling: History and Mystery of Large Amplitude Motions over a Century.The journal of physical chemistry letters · 2025Review
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
Chiral molecules with low enantiomer interconversion barriers racemize even at cryogenic temperatures due to quantum tunneling, forming a racemic mixture that is impossible to separate using conventional chemical methods. Here we both experimentally and theoretically demonstrate a method to create and probe a state-specific enantiomeric enrichment for such molecular systems. The coherent, non-linear, and resonant approach is based on a microwave six-wave mixing scheme and consists of five phase-controlled microwave pulses. The first three pulses induce a chiral wavepacket in a chosen rotational state, while the consecutive two pulses induce a polarization for a particular rotational transition (listen transition) with a magnitude proportional to the enantiomeric excess created. The experiments are performed with the transiently chiral molecule benzyl alcohol, where a chiral molecular response was successfully obtained. This signal demonstrates that enantiomeric excess can be induced in a quantum racemic mixture of a transiently chiral molecule using the developed microwave six-wave mixing scheme, which is an important step towards controlling non-rigid chiral molecular systems.
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Registered trials
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