# A Controlled System for Parahydrogen Hyperpolarization Experiments

**Authors:** Lorenzo Franco, Federico Floreani, Salvatore Mamone, Ahmed Mohammed Faramawy, Marco Ruzzi, Cristina Tubaro, Gabriele Stevanato

PMC · DOI: 10.3390/molecules30214299 · Molecules · 2025-11-05

## TL;DR

This paper introduces a portable and cost-effective system for parahydrogen-induced hyperpolarization experiments, enabling easier and more versatile NMR signal amplification.

## Contribution

A compact, controllable setup for PHIP and SABRE experiments that works across ultra-low and high magnetic fields.

## Key findings

- The system enables precise control of bubbling pressure, temperature, and gas flow for hyperpolarization studies.
- The Ir–IMes catalyst's activation time and response to parahydrogen flow and pressure were systematically explored.
- The Ir–SIPr catalyst was demonstrated as a viable alternative for pyruvate hyperpolarization.

## Abstract

Parahydrogen-induced hyperpolarization (PHIP), introduced nearly four decades ago, provides an elegant solution to one of the fundamental limitations of nuclear magnetic resonance (NMR)—its notoriously low sensitivity. By converting the spin order of parahydrogen into nuclear spin polarization, NMR signals can be boosted by several orders of magnitude. Here we present a portable, compact, and cost-effective setup that brings PHIP and Signal Amplification by Reversible Exchange (SABRE) experiments within easy reach, operating seamlessly across ultra-low-field (0–10 μT) and high-field (>1 T) conditions at 50% parahydrogen enrichment. The system provides precise control over bubbling pressure, temperature, and gas flow, enabling systematic studies of how these parameters shape hyperpolarization performance. Using the benchmark Chloro(1,5-cyclooctadiene)[1,3-bis(2,4,6-trimethylphenyl)imidazole-2-ylidene]iridium(I) (Ir–IMes) catalyst, we explore the catalyst activation time and response to parahydrogen flow and pressure. Polarization transfer experiments from hydrides to [1-13C]pyruvate leading to the estimation of heteronuclear J-couplings are also presented. We further demonstrate the use of Chloro(1,5-cyclooctadiene)[1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene]iridium(I) (Ir–SIPr), a recently introduced catalyst that can also be used for pyruvate hyperpolarization. The proposed design is robust, reproducible, and easy to implement in any laboratory, widening the route to explore and expand the capabilities of parahydrogen-based hyperpolarization.

## Full-text entities

- **Chemicals:** Chloro(1,5-cyclooctadiene)[1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene]iridium(I) (-), pyruvate (MESH:D019289)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12608504/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC12608504/full.md

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Source: https://tomesphere.com/paper/PMC12608504