Dissolution dynamic nuclear polarization of deuterated molecules enhanced by cross-polarization

We present novel means to hyperpolarize deuterium nuclei in 13CD2 groups at cryogenic temperatures. The method is based on cross-polarization from 1H to 13C and does not require any radio-frequency fields applied to the deuterium nuclei. After rapid dissolution, a new class of long-lived spin states...

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Veröffentlicht in:The Journal of chemical physics 2016-11, Vol.145 (19), p.194203-194203
Hauptverfasser: Kurzbach, Dennis, Weber, Emmanuelle M. M., Jhajharia, Aditya, Cousin, Samuel F., Sadet, Aude, Marhabaie, Sina, Canet, Estel, Birlirakis, Nicolas, Milani, Jonas, Jannin, Sami, Eshchenko, Dmitry, Hassan, Alia, Melzi, Roberto, Luetolf, Stephan, Sacher, Marco, Rossire, Marc, Kempf, James, Lohman, Joost A. B., Weller, Matthias, Bodenhausen, Geoffrey, Abergel, Daniel
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Sprache:eng
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Zusammenfassung:We present novel means to hyperpolarize deuterium nuclei in 13CD2 groups at cryogenic temperatures. The method is based on cross-polarization from 1H to 13C and does not require any radio-frequency fields applied to the deuterium nuclei. After rapid dissolution, a new class of long-lived spin states can be detected indirectly by 13C NMR in solution. These long-lived states result from a sextet-triplet imbalance (STI) that involves the two equivalent deuterons with spin I = 1. An STI has similar properties as a triplet-singlet imbalance that can occur in systems with two equivalent I = 1 2 spins. Although the lifetimes T STI are shorter than T 1(Cz), they can exceed the life-time T 1(Dz) of deuterium Zeeman magnetization by a factor of more than 20.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.4967402