Abstract
Abstract
Dissolution-dynamic nuclear polarization (d-DNP) is a hyperpolarization technique that is used to enhance the sensitivity of liquid-state nuclear magnetic resonance (NMR) in biophysical and chemical applications. D-DNP is used widely for the sensitivity enhancement of hetero-nuclei such as
13
C, but it is barely used for
1
H hyperpolarization, despite the abundance of
1
H in organic matter. Here we show that OX063, a radical that has so far been used only for the hyperpolarization of low-
γ
nuclei such as
13
C, may be used also to hyperpolarize
1
H. This hyperpolarization route is enabled by the use of a klystron amplifier that provides three orders of magnitude more power than conventionally used solid-state microwave sources. Following hyperpolarization, the sample is ejected from the polarizer and liquefied, yielding
1
H signal enhancements of ~ 1000 in high-field NMR. The use of OX063 limits not only
T
1
relaxation during sample transfer, but we also show that it preserves the liquid-state
T
2
, and therefore offers superior sensitivity and resolution. The applicability of this method to polarize
1
H of selected amino acids is demonstrated.