Hb. Stuhrmann et al., POLARIZED NEUTRON-SCATTERING FROM POLARIZED NUCLEI NEAR PARAMAGNETIC CENTERS, Journal of applied crystallography, 30(2), 1997, pp. 839-843
Polarized neutron scattering from dynamically polarized targets has be
en used for the study of hydrogenous materials in several laboratories
. A new variant, which is less dependent on specific deuteration, is p
roposed. This is based on the observation that a radio frequency (RF)
held swept over a selected part of an NMR line depolarizes the spins d
epending on their spatial distribution in and around paramagnetic mole
cules. An RF field swept over a narrow frequency interval has little e
ffect on polarized nuclear spins in the paramagnetic centers, whereas
remote nuclear spins can be depolarized. When applying the sweep over
a much larger frequency range, all spins are depolarized. This was obs
erved both by NMR and by polarized neutron scattering after selective
depolarization of the proton spins in a solid solution of protonated E
HBA-Cr-V, Na(C12H20O7CrV). D2O, in a mixture of deuterated glycerol an
d water. The decay time of proton spin polarization in domains associa
ted with the paramagnetic centers varies between 5 h in a deuterated s
olvent and less than 1 min in a protonated solvent. The size of such a
domain is barely larger than 1 nm. The same observation is also made
when the nuclear polarization is reversed by adiabatic fast passage. I
f the RF sweep is limited to frequencies close to the central peak of
the proton NMR line, the proton spins far away from the paramagnetic c
enters are reversed, whereas those of EHBA-Cr-V and close to the cente
rs maintain their original polarization. This method may become a usef
ul tool in neutron scattering once the paramagnetic centers can be fix
ed as spin labels to well defined sites in a macromolecule, preferably
in a crystal lattice.