6533b852fe1ef96bd12ab866

RESEARCH PRODUCT

Constant-adiabaticity ultralow magnetic field manipulations of parahydrogen-induced polarization: application to an AA'X spin system

Román Picazo-frutosKirill F. SheberstovBogdan A. RodinKonstantin L. IvanovJames EillsDmitry BudkerDmitry Budker

subject

PhysicsField (physics)General Physics and Astronomy02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologySpin isomers of hydrogenPolarization (waves)01 natural sciencesInduced polarization0104 chemical sciencesMagnetic fieldPhysics - Chemical PhysicsChemical additionProton spin crisisPhysical and Theoretical ChemistryAtomic physics0210 nano-technologySpin-½

description

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 substrate via chemical addition of H2 in the spin-singlet state, but it is typically necessary to transfer the proton polarization to a heteronucleus (usually 13C) 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.

https://doi.org/10.1039/d0cp06581a