Liquid-State 13C Polarization of 30% through Photoinduced Nonpersistent Radicals
Author(s) -
Andrea Capozzi,
Magnus Karlsson,
Jan Raagaard Petersen,
Mathilde H. Lerche,
Jan Henrik ArdenkjærLarsen
Publication year - 2018
Publication title -
the journal of physical chemistry c
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 289
eISSN - 1932-7455
pISSN - 1932-7447
DOI - 10.1021/acs.jpcc.8b01482
Subject(s) - hyperpolarization (physics) , spins , polarization (electrochemistry) , radical , magnet , nuclear magnetic resonance , chemistry , materials science , physics , nuclear magnetic resonance spectroscopy , condensed matter physics , organic chemistry , quantum mechanics
Hyperpolarization via dissolution dynamic nuclear polarization (dDNP) is crucial to significantly increasing the magnetic resonance imaging (MRI) sensitivity, opening up in vivo real-time MRI using 13C-labeled substrates. The range of applications, however, is limited by the relatively fast decay of the nuclear spin polarization together with the constraint of having to polarize the spins near the MRI magnet. As recently demonstrated, the employment of UV-induced nonpersistent radicals represents an elegant solution to tackling these drawbacks. Nevertheless, since its introduction, the spread of the technique has been prevented by the relatively low achievable polarization, slow buildup time, and time-consuming sample preparation. In the present work, thanks to a thorough investigation of the radical generation step, we provide a robust protocol to enhance the efficiency and performance of the UV-radical technique. Under optimal conditions, it was possible to produce up to 60 mM radical in less than 5 min...
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