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Polarization transfer efficiency in PHIP experiments.

作者信息

Emondts M, Colell J F P, Blümich B, Schleker P P M

机构信息

RWTH Aachen University, Institut für Technische und Makromolekulare Chemie, Worringer Weg 1, 52074 Aachen, Germany.

出版信息

Phys Chem Chem Phys. 2017 Aug 23;19(33):21933-21937. doi: 10.1039/c7cp04296e.

DOI:10.1039/c7cp04296e
PMID:28808726
Abstract

Parahydrogen induced polarization (PHIP) is a hyperpolarization method for NMR signal enhancement with applications in spectroscopy and imaging. Although parahydrogen can be easily enriched up to nearly 95%, the polarization detected on the hydrogenated substrate is substantially lower, where numerous loss mechanisms between the start of the hydrogenation reaction and detection affect polarization levels. The quality of PHIP systems is commonly determined by stating either the polarization degree or the enhancement factor of the product at the time of detection. In this study, we present a method that allows the distinction of polarization loss due to both the catalytic cycle and T relaxation of the formed product prior to detection. We determine the influence of homogeneous catalysts and define a rigorous measure of the polarization transfer efficiency (PTE). Our results show that the PTE strongly depends on the concentration of all components and the chemical structure of the catalyst as well as on the magnetic field of detection.

摘要

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