Climbing the rotational ladder to chirality
arXiv:1802.07803 · doi:10.1103/PhysRevLett.121.193201
Abstract
Molecular chirality is conventionally understood as space-inversion-symmetry breaking in the equilibrium structure of molecules. Less well known is that achiral molecules can be made chiral through extreme rotational excitation. Here, we theoretically demonstrate a clear strategy for generating rotationally-induced chirality (RIC): An optical centrifuge rotationally excites the phosphine molecule (PH) into chiral cluster states that correspond to clockwise (-enantiomer) or anticlockwise (-enantiomer) rotation about axes almost coinciding with single P-H bonds. Application of a strong dc electric field during the centrifuge pulse favors the production of one rotating enantiomeric form over the other, creating dynamically chiral molecules with oriented rotational angular momentum. This essential step toward characterizing RIC promises a fresh perspective on chirality as a fundamental aspect of nature.
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Cited by in corpus (14)
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- Molecular movie of ultrafast coherent rotational dynamics
- Ultrafast chirality: the road to efficient chiral measurements
- Controlled enantioselective orientation of chiral molecules with an optical centrifuge
- Field-induced diastereomers for chiral separation
- Imprinting chirality on atoms using synthetic chiral light fields
- The high-temperature rotation-vibration spectrum and rotational clustering of silylene (SiH)
- Rotation of polarization of light propagating through a gas of molecular super-rotors
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- Quantum control of ro-vibrational dynamics and application to light-induced molecular chirality
- Controlling rotation in the molecular-frame with an optical centrifuge
- Time-resolving the UV-initiated photodissociation dynamics of OCS
- Phase-matched locally chiral light for global control of chiral light-matter interaction
- Polarization of chirality