Quantum control of radical pair reactions by local optimization theory (original) (raw)

Anisotropic and Coherent Control of Radical Pairs by Optimized RF Fields

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Quantum Control of Radical-Pair Dynamics beyond Time-Local Optimization

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Theoretical and experimental studies of chemically induced electron-nuclear polarization in low magnetic fields

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Magnetic Field Dependence of Electron Spin Polarization Generated through Radical−Triplet Interactions

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An open quantum system approach to the radical pair mechanism

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Magnetic field effects on the dynamic behavior of a radical pair involving a germyl radical

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Electron spin exchange in micellized radical pairs. I. 13C low field chemically induced dynamic nuclear polarization (CIDNP) and 13C radio frequency stimulated nuclear polarization (SNP)

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Reaction operators for spin-selective chemical reactions of radical pairs

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Quantum beats in confined radical pairs at a strong pulse microwave field

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Magnetic Field Effects Due to the Δ g Mechanism upon Chemical Reactions through Radical Pairs under Ultrahigh Fields of up to 30 T

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Optical switching of radical pair conformation enhances magnetic sensitivity

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Control of Singlet-Precursor Radical Pair Lifetime by Manipulation of Spin-Selective Reaction Pathways

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Electron Spin Polarization Transfer from Photogenerated Spin-Correlated Radical Pairs to a Stable Radical Observer Spin

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Electron spin exchange in micellized radical pairs. III. 13C low-field ratio frequency stimulated nuclear polarization spectroscopy (LF SNP)

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Triplet Radical Interaction. Direct Measurement of Triplet Polarization Transfer by Fourier Transform Electron Paramagnetic Resonance

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Quantum Beats of the Radical Pair State in Photosynthetic Models Observed by Transient Electron Paramagnetic Resonance

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Theory of optically detected magnetic resonance spectra of radical pairs

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Exploiting adiabatically switched RF-field for manipulating spin hyperpolarization induced by parahydrogen

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