期刊
JOURNAL OF CHEMICAL PHYSICS
卷 131, 期 19, 页码 -出版社
AMER INST PHYSICS
DOI: 10.1063/1.3254386
关键词
chemical shift; hydrogen; magnetisation
资金
- EPSRC [EP/F022530/1, EP/G009546/1] Funding Source: UKRI
- Engineering and Physical Sciences Research Council [EP/F022530/1, EP/G009546/1, GR/S23605/01] Funding Source: researchfish
- Biotechnology and Biological Sciences Research Council Funding Source: Medline
- Medical Research Council Funding Source: Medline
When parahydrogen adds to a metal template containing a substrate of interest, the substrate and parahydrogen become coupled, and polarization is shared between the two without the incorporation of the parahydrogen into the substrate. A mechanism for this polarization transfer is presented in which the transfer is propagated through the scalar couplings. At zero field, polarization is transferred between two-, three-, and four-spin zero quantum states, but no single spin magnetization is created. The interplay between the chemical shift evolution and the evolution under scalar coupling at non-zero field generates additional longitudinal spin order and now includes single spin longitudinal z-magnetization. The additional chemical shift interaction introduces a field dependency to the nuclear spin states of the polarized substrate. The net effect of the polarization field strength on the resultant nuclear spin states is shown to be predictable but complex.
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