dc.contributor.author | Tan, Kong Ooi | |
dc.contributor.author | Mardini, Michael | |
dc.contributor.author | Yang, Chen | |
dc.contributor.author | Ardenkjaer-Larsen, Jan-Henrik | |
dc.contributor.author | Griffin, Robert Guy | |
dc.date.accessioned | 2020-06-23T16:00:29Z | |
dc.date.available | 2020-06-23T16:00:29Z | |
dc.date.issued | 2019-07 | |
dc.identifier.issn | 2375-2548 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/125933 | |
dc.description.abstract | Dynamic nuclear polarization (DNP) has evolved as the method of choice to enhance NMR signal intensities and to address a variety of otherwise inaccessible chemical, biological and physical questions. Despite its success, there is no detailed understanding of how the large electron polarization is transferred to the surrounding nuclei or where these nuclei are located relative to the polarizing agent. To address these questions we perform an analysis of the three-spin solid effect, and show that it is exquisitely sensitive to the electron-nuclear distances. We exploit this feature and determine that the size of the spin diffusion barrier surrounding the trityl radical in a glassy glycerol–water matrix is <6 Å, and that the protons involved in the initial transfer step are on the trityl molecule. 1H ENDOR experiments indicate that polarization is then transferred in a second step to glycerol molecules in intimate contact with the trityl. | en_US |
dc.language.iso | en | |
dc.publisher | American Association for the Advancement of Science (AAAS) | en_US |
dc.relation.isversionof | 10.1126/SCIADV.AAX2743 | en_US |
dc.rights | Creative Commons Attribution NonCommercial License 4.0 | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/4.0/ | en_US |
dc.source | Science Advances | en_US |
dc.title | Three-spin solid effect and the spin diffusion barrier in amorphous solids | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Tan, Kong Ooi, et al., "Three-spin solid effect and the spin diffusion barrier in amorphous solids." Science Advances 5, 7 (July 2019): no. eaax2743 doi 10.1126/SCIADV.AAX2743 ©2019 Author(s) | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Chemistry | en_US |
dc.contributor.department | Francis Bitter Magnet Laboratory (Massachusetts Institute of Technology) | en_US |
dc.relation.journal | Science Advances | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2019-12-18T13:49:08Z | |
dspace.date.submission | 2019-12-18T13:49:10Z | |
mit.journal.volume | 5 | en_US |
mit.journal.issue | 7 | en_US |
mit.metadata.status | Complete | |