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IrTMes – a stable SABRE catalyst for the hyperpolarization of [1- $^{13}$C]-pyruvate

Wacker, Jakoba 1; Korvink, Jan G. 1; Lehmkuhl, Sören ORCID iD icon 1
1 Institut für Mikrostrukturtechnik (IMT), Karlsruher Institut für Technologie (KIT)

Abstract:

Signal amplification by reversible exchange (SABRE) can enhance nuclear magnetic resonance (NMR) signals by catalyzing the transfer of spin order from para-hydrogen to a substrate via transient coordination of both to an iridium complex. An important target substrate due to its biomedical relevance is [1-13C]-pyruvate. Hyperpolarizing [1-13C]-pyruvate in an acetone water mixture (Ace-SABRE) increases the biocompatibility of hyperpolarized [1-13C]-pyruvate due to easier solvent removal. However, the Ace-SABRE solvent system causes rapid deactivation of the catalyst, requiring frequent renewal of the sample. Here, we introduce a more resource-efficient Ace-SABRE catalyst IrTMes, where the iridium center is ligated with 1,4-dimesityl-3-methyl-1,2,3-triazol-5-ylidene. At a para-hydrogen pressure of 5.17 bar, the IrTMes catalyst exhibits 17-times longer-lasting functionality under Ace-SABRE conditions and four times under exposure to the atmosphere compared to IrIMes at room temperature. This increased stability of IrTMes allows for reproducible and repeatable SABRE experiments. IrTMes achieves a signal enhancement of around 5000 at 50% para-hydrogen enrichment at 1.45 T, which corresponds to a polarization level of 0.62% or around 1.9% when extrapolated for 100% para-hydrogen. ... mehr


Verlagsausgabe §
DOI: 10.5445/IR/1000198299
Veröffentlicht am 26.10.2026
Originalveröffentlichung
DOI: 10.1039/d6an00328a
Scopus
Zitationen: 1
Web of Science
Zitationen: 1
Cover der Publikation
Zugehörige Institution(en) am KIT Institut für Mikrostrukturtechnik (IMT)
Publikationstyp Zeitschriftenaufsatz
Publikationsdatum 24.08.2026
Sprache Englisch
Identifikator ISSN: 0003-2654, 1364-5528
KITopen-ID: 1000198299
Erschienen in The Analyst
Verlag Royal Society of Chemistry (RSC)
Band 151
Heft 17
Seiten 4941–4949
Nachgewiesen in Scopus
Web of Science
OpenAlex
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