dc.contributor.author
Kiryutin, Alexey S.
dc.contributor.author
Ivanov, Konstantin L.
dc.contributor.author
Yurkowskaya, Alexandra
dc.contributor.author
Kaptein, Robert
dc.contributor.author
Vieth, Hans-Martin
dc.date.accessioned
2018-06-08T03:41:24Z
dc.date.available
2014-03-06
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15717
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-19904
dc.description.abstract
Para-Hydrogen Induced Polarization (PHIP) experiments were performed in
coupled multispin systems at variable magnetic fields. We studied the magnetic
field dependence of PHIP in styrene, which is the product of hydrogenation of
phenylacetylene. At low magnetic fields where the spins are coupled strongly
by scalar interaction efficient polarization transfer among the interacting
protons takes place. The experimentally observed spectra are in good agreement
with the simulation, which takes into account eight coupled spins. We also
demonstrate effects of nuclear spin level anti-crossings on the PHIP pattern.
It is shown that rapid passage through the level anti-crossing enables highly
efficient polarization transfer between specific spin orders. In addition, we
studied PHIP transfer to 13C and 19F hetero-nuclei. It is shown that hetero-
nuclei can be efficiently polarized in a wide field range; in particular, for
polarizing them it is not necessary to go to ultra-low fields, which provide
their strong coupling to protons. The resulting polarization is of the
multiplet type and gives strong enhancements of the individual NMR lines. In
general, variation of the magnetic field gives the opportunity for
manipulating PHIP patterns and transferring polarization to target spins of
choice.
en
dc.rights.uri
http://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik
dc.title
Transfer of Parahydrogen Induced Polarization in Scalar Coupled Systems at
Variable Magnetic Field
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Zeitschrift für Physikalische Chemie. - 226 (2012), 11/12, S. 1343-1362
dc.identifier.sepid
29665
dcterms.bibliographicCitation.doi
10.1524/zpch.2012.0307
dcterms.bibliographicCitation.url
http://dx.doi.org/10.1524/zpch.2012.0307
refubium.affiliation
Physik
de
refubium.affiliation.other
Institut für Experimentalphysik
refubium.mycore.fudocsId
FUDOCS_document_000000019803
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000003172
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
0942-9352