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      Full quantum control of enantiomer-selective state transfer in chiral molecules despite degeneracy

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          Abstract

          The driven quantum asymmetric top is an important paradigm in molecular physics with applications ranging from quantum information to chiral-sensitive spectroscopy. A key prerequisite for these applications is the ability to completely control the rotational dynamics. The inherent degeneracy of quantum rotors poses a challenge for quantum control since selecting a particular rotational state cannot be achieved by spectral selection alone. Here, we prove complete controllability for rotational states of an asymmetric top belonging to degenerate values of the orientational quantum number M. Based on this insight, we construct a pulse sequence that energetically separates population in degenerate M-states. Introducing the concept of enantio-selective controllability, we determine the conditions for complete enantiomer-specific population transfer in chiral molecules and construct pulse sequences for the example of propanediol and carvone molecules for population initially distributed over degenerate M-states. Our work shows how to leverage controllability analysis for the solution of practical quantum control problems.

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          Most cited references49

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          Quantum computation with trapped polar molecules.

          D DeMille (2002)
          We propose a novel physical realization of a quantum computer. The qubits are electric dipole moments of ultracold diatomic molecules, oriented along or against an external electric field. Individual molecules are held in a 1D trap array, with an electric field gradient allowing spectroscopic addressing of each site. Bits are coupled via the electric dipole-dipole interaction. Using technologies similar to those already demonstrated, this design can plausibly lead to a quantum computer with greater, approximately > or = 10(4) qubits, which can perform approximately 10(5) CNOT gates in the anticipated decoherence time of approximately 5 s.
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            Training Schrödinger’s cat: quantum optimal control

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              Enantiomer-specific detection of chiral molecules via microwave spectroscopy.

              Chirality plays a fundamental part in the activity of biological molecules and broad classes of chemical reactions, but detecting and quantifying it remains challenging. The spectroscopic methods of choice are usually circular dichroism and vibrational circular dichroism, methods that are forbidden in the electric dipole approximation. The resultant weak effects produce weak signals, and thus require high sample densities. In contrast, nonlinear techniques probing electric-dipole-allowed effects have been used for sensitive chiral analyses of liquid samples. Here we extend this class of approaches by carrying out nonlinear resonant phase-sensitive microwave spectroscopy of gas phase samples in the presence of an adiabatically switched non-resonant orthogonal electric field; we use this technique to map the enantiomer-dependent sign of an electric dipole Rabi frequency onto the phase of emitted microwave radiation. We outline theoretically how this results in a sensitive and species-selective method for determining the chirality of cold gas-phase molecules, and implement it experimentally to distinguish between the S and R enantiomers of 1,2-propanediol and their racemic mixture. This technique produces a large and definitive signature of chirality, and has the potential to determine the chirality of multiple species in a mixture.
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                Author and article information

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                Journal
                Communications Physics
                Commun Phys
                Springer Science and Business Media LLC
                2399-3650
                December 2022
                May 06 2022
                December 2022
                : 5
                : 1
                Article
                10.1038/s42005-022-00883-6
                adcae1b2-17dc-4042-9c39-f99e821f8acf
                © 2022

                https://creativecommons.org/licenses/by/4.0

                https://creativecommons.org/licenses/by/4.0

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