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Updated: Sep 21, 2025

Hyperpolarized Xenon for NMR and MRI Applications
Published on: September 6, 2012
Advancing homogeneous catalysis for parahydrogen-derived hyperpolarisation and its NMR applications
Ben J Tickner1,2, Vladimir V Zhivonitko1
1NMR Research Unit, Faculty of Science, University of Oulu P.O. Box 3000 Oulu 90014 Finland ben.tickner@alumni.york.ac.uk vladimir.zhivonitko@oulu.fi.
Abstract:
Parahydrogen-induced polarisation (PHIP) is a nuclear spin hyperpolarisation technique employed to enhance NMR signals for a wide range of molecules. This is achieved by exploiting the chemical reactions of parahydrogen (para-H2), the spin-0 isomer of H2. These reactions break the molecular symmetry of para-H2 in a way that can produce dramatically enhanced NMR signals for reaction products, and are usually catalysed by a transition metal complex. In this review, we discuss recent advances in novel homogeneous catalysts that can produce hyperpolarised products upon reaction with para-H2. We also discuss hyperpolarisation attained in reversible reactions (termed signal amplification by reversible exchange, SABRE) and focus on catalyst developments in recent years that have allowed hyperpolarisation of a wider range of target molecules. In particular, recent examples of novel ruthenium catalysts for trans and geminal hydrogenation, metal-free catalysts, iridium sulfoxide-containing SABRE systems, and cobalt complexes for PHIP and SABRE are reviewed. Advances in this catalysis have expanded the types of molecules amenable to hyperpolarisation using PHIP and SABRE, and their applications in NMR reaction monitoring, mechanistic elucidation, biomedical imaging, and many other areas, are increasing.
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