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Journal Article | PUBDB-2019-03812 |
; ; ; ;
2019
APS
College Park, Md.
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Please use a persistent id in citations: doi:10.1103/PhysRevLett.123.243202 doi:10.3204/PUBDB-2019-03812
Report No.: arXiv:1905.07166
Abstract: A novel approach for the state-specific enantiomeric enrichment and the spatial separation ofenantiomers is presented. Our scheme utilizes techniques from strong-field laser physics, specificallyan optical centrifuge in conjunction with a static electric field, to create a chiral field with definedhandedness. Molecular enantiomers experience unique rotational excitation dynamics and thiscan be exploited to spatially separate the enantiomers using electrostatic deflection. Notably, therotational-state-specific enantiomeric enhancement and its handedness is fully controllable. Toexplain these effects, the conceptual framework of field-induced diastereomers of a chiral molecule isintroduced and computationally demonstrated through robust quantum-mechanical simulations onthe prototypical chiral molecule propylene oxide (C$_3$H$_6$O), for which ensembles with an enantiomericexcess of up to 30 % were obtained.
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Field-Induced Diastereomers for Chiral Separation
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