<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cordova M</submitter><funding>Swiss National Science Foundation</funding><pagination>e202216607</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10107932</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>62(8)</volume><pubmed_abstract>The resolution of proton solid-state NMR spectra is usually limited by broadening arising from dipolar interactions between spins. Magic-angle spinning alleviates this broadening by inducing coherent averaging. However, even the highest spinning rates experimentally accessible today are not able to completely remove dipolar interactions. Here, we introduce a deep learning approach to determine pure isotropic proton spectra from a two-dimensional set of magic-angle spinning spectra acquired at different spinning rates. Applying the model to 8 organic solids yields high-resolution &lt;sup>1&lt;/sup> H solid-state NMR spectra with isotropic linewidths in the 50-400 Hz range.</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Pure Isotropic Proton NMR Spectra in Solids using Deep Learning.</pubmed_title><pmcid>PMC10107932</pmcid><funding_grant_id>200020</funding_grant_id><funding_grant_id>212046</funding_grant_id><funding_grant_id>NCCR MARVEL</funding_grant_id><funding_grant_id>200020_212046</funding_grant_id><pubmed_authors>Cordova M</pubmed_authors><pubmed_authors>Emsley L</pubmed_authors><pubmed_authors>Torodii D</pubmed_authors><pubmed_authors>Simoes de Almeida B</pubmed_authors><pubmed_authors>Moutzouri P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pure Isotropic Proton NMR Spectra in Solids using Deep Learning.</name><description>The resolution of proton solid-state NMR spectra is usually limited by broadening arising from dipolar interactions between spins. Magic-angle spinning alleviates this broadening by inducing coherent averaging. However, even the highest spinning rates experimentally accessible today are not able to completely remove dipolar interactions. Here, we introduce a deep learning approach to determine pure isotropic proton spectra from a two-dimensional set of magic-angle spinning spectra acquired at different spinning rates. Applying the model to 8 organic solids yields high-resolution &lt;sup>1&lt;/sup> H solid-state NMR spectra with isotropic linewidths in the 50-400 Hz range.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-07-10T03:08:21.145Z</modification><creation>2025-04-06T11:21:07.698Z</creation></dates><accession>S-EPMC10107932</accession><cross_references><pubmed>36562545</pubmed><doi>10.1002/anie.202216607</doi></cross_references></HashMap>