<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pravdivtsev AN</submitter><funding>DFG-RFBR</funding><funding>Emmy Noether Program "metabolic and molecular MR"</funding><funding>research training circle "materials for brain"</funding><funding>European Regional Development Fund (ERDF)</funding><funding>Cluster of Excellence "precision medicine in inflammation"</funding><funding>German Federal Ministry of Education and Research (BMBF)</funding><funding>Zukunftsprogramm Wirtschaft of Schleswig-Holstein</funding><funding>e:Med</funding><funding>Kiel University</funding><pagination>667-672</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7187451</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(7)</volume><pubmed_abstract>Nuclear Magnetic Resonance (NMR) is an intriguing quantum-mechanical effect that is used for routine medical diagnostics and chemical analysis alike. Numerous advancements have contributed to the success of the technique, including hyperpolarized contrast agents that enable real-time imaging of metabolism in vivo. Herein, we report the finding of an NMR radio amplification by stimulated emission of radiation (RASER), which continuously emits 1 H NMR signal for more than 10 min. Using parahydrogen induced hyperpolarization (PHIP) with 50 % para-hydrogen, we demonstrated the effect at 600 MHz but expect that it is functional across a wide range of frequencies, e.g. 101 -103  MHz. PHIP-RASER occurs spontaneously or can be triggered with a standard NMR excitation. Full chemical shift resolution was maintained, and a linewidth of 0.6 ppb was achieved. The effect was reproduced by simulations using a weakly coupled, two spin- 1/2 system. All devices used were standard issue, such that the effect can be reproduced by any NMR lab worldwide with access to liquid nitrogen for producing parahydrogen.</pubmed_abstract><journal>Chemphyschem : a European journal of chemical physics and physical chemistry</journal><pubmed_title>Continuous Radio Amplification by Stimulated Emission of Radiation using Parahydrogen Induced Polarization (PHIP-RASER) at 14 Tesla.</pubmed_title><pmcid>PMC7187451</pmcid><funding_grant_id>GRK 2154/1-2019</funding_grant_id><funding_grant_id>1267</funding_grant_id><funding_grant_id>122-09-053</funding_grant_id><funding_grant_id>4604/2-2</funding_grant_id><funding_grant_id>4604/3-1</funding_grant_id><funding_grant_id>01ZX1915C</funding_grant_id><funding_grant_id>19-53-12013</funding_grant_id><pubmed_authors>Pravdivtsev AN</pubmed_authors><pubmed_authors>Sonnichsen FD</pubmed_authors><pubmed_authors>Hovener JB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Continuous Radio Amplification by Stimulated Emission of Radiation using Parahydrogen Induced Polarization (PHIP-RASER) at 14 Tesla.</name><description>Nuclear Magnetic Resonance (NMR) is an intriguing quantum-mechanical effect that is used for routine medical diagnostics and chemical analysis alike. Numerous advancements have contributed to the success of the technique, including hyperpolarized contrast agents that enable real-time imaging of metabolism in vivo. Herein, we report the finding of an NMR radio amplification by stimulated emission of radiation (RASER), which continuously emits 1 H NMR signal for more than 10 min. Using parahydrogen induced hyperpolarization (PHIP) with 50 % para-hydrogen, we demonstrated the effect at 600 MHz but expect that it is functional across a wide range of frequencies, e.g. 101 -103  MHz. PHIP-RASER occurs spontaneously or can be triggered with a standard NMR excitation. Full chemical shift resolution was maintained, and a linewidth of 0.6 ppb was achieved. The effect was reproduced by simulations using a weakly coupled, two spin- 1/2 system. All devices used were standard issue, such that the effect can be reproduced by any NMR lab worldwide with access to liquid nitrogen for producing parahydrogen.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Apr</publication><modification>2024-11-08T12:16:31.614Z</modification><creation>2020-05-22T18:36:58Z</creation></dates><accession>S-EPMC7187451</accession><cross_references><pubmed>31898393</pubmed><doi>10.1002/cphc.201901056</doi></cross_references></HashMap>