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@ARTICLE{Emondts:836100,
author = {Emondts, M. and Colell, J. and Blümich, B. and Schleker,
Peter Philipp Maria},
title = {{P}olarization {T}ransfer {E}fficiency in {PHIP}
{E}xperiments},
journal = {Physical chemistry, chemical physics},
volume = {19},
number = {33},
issn = {1463-9084},
address = {Cambridge},
publisher = {RSC Publ.},
reportid = {FZJ-2017-05224},
pages = {21933-21937},
year = {2017},
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 T1 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.},
cin = {IEK-9},
ddc = {540},
cid = {I:(DE-Juel1)IEK-9-20110218},
pnm = {131 - Electrochemical Storage (POF3-131)},
pid = {G:(DE-HGF)POF3-131},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000408257700002},
doi = {10.1039/C7CP04296E},
url = {https://juser.fz-juelich.de/record/836100},
}