Abstract
The field of magnetic resonance imaging with hyperpolarized contrast agents is rapidly expanding, and parahydrogen-induced polarization (PHIP) is emerging as an inexpensive and easy-to-implement method for generating the required hyperpolarized biomolecules. Hydrogenative PHIP delivers hyperpolarized proton spin order to a substrateviachemical addition of H2in the spin-singlet state, but it is typically necessary to transfer the proton polarization to a heteronucleus (usually13C) which has a longer spin lifetime. Adiabatic ultralow magnetic field manipulations can be used to induce the polarization transfer, but this is necessarily a slow process, which is undesirable since the spins continually relax back to thermal equilibrium. Here we demonstrate two constant-adiabaticity field sweep methods, one in which the field passes through zero, and one in which the field is swept from zero, for optimal polarization transfer on a model AA′X spin system, [1-13C]fumarate. We introduce a method for calculating the constant-adiabaticity magnetic field sweeps, and demonstrate that they enable approximately one order of magnitude faster spin-order conversion compared to linear sweeps. The present method can thus be utilized to manipulate nonthermal order in heteronuclear spin systems.
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CITATION STYLE
Rodin, B. A., Eills, J., Picazo-Frutos, R., Sheberstov, K. F., Budker, D., & Ivanov, K. L. (2021). Constant-adiabaticity ultralow magnetic field manipulations of parahydrogen-induced polarization: application to an AA’X spin system. Physical Chemistry Chemical Physics, 23(12), 7125–7134. https://doi.org/10.1039/d0cp06581a
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