Robust nuclear hyperpolarization of small molecules through intermolecular transfer of parahydrogen-derived polarization
The recent advent of hyperpolarization techniques, which can enhance NMR signals by several orders of magnitude relative to thermally polarized samples, has enabled applications traditionally out of reach due to the inherently low sensitivity of NMR techniques. However, a high barrier to entry remains, as most hyperpolarization approaches either require complex instrumentation or are applicable only to a relatively small set of molecules. Here we introduce PHIPNOE, a platform that directly addresses both limitations. PHIPNOE is based on parahydrogen-induced polarization (PHIP), which is well-established as a scalable route to hyperpolarization requiring minimal instrumentation, but has been mostly restricted to molecules that undergo specific chemical reactions. We overcome this barrier by tailoring PHIP to create highly polarized, highly concentrated solutions of one specific molecule, which acts as an intermediate source of polarization. This 'source molecule' then distributes polarization to a broad range of target molecules mixed into the solution, via the spin polarization-induced nuclear Overhauser effect (SPINOE). We investigate chemical influences on PHIPNOE, and develop a predictive model to estimate enhancement based on molecular mass and T1 relaxation times. A complete run from PHIP hyperpolarization to PHIPNOE polarization transfer and signal detection takes less than one minute, the approach does not require any modifications to the NMR spectrometer, and enhancements are repeatable across molecular classes. PHIPNOE thus enables applications including single-shot multidimensional NMR, real-time monitoring of dynamic processes, and, with 300-fold signal amplification demonstrated on a benchtop spectrometer, practical low-field NMR, where we show enhanced sensitivity in detecting per- and polyfluoroalkyl substances (PFAS).