<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>61(40)</volume><submitter>Merakeb L</submitter><pubmed_abstract>Nitrogen reduction under mild conditions (room T and atmospheric P), using a non-fossil source of hydrogen remains a challenge. Molecular metal complexes, notably Mo based, have recently been shown to be active for such nitrogen fixation. We report electrochemical N&lt;sub>2&lt;/sub> splitting with a Mo&lt;sup>III&lt;/sup> triphosphino complex [(PPP)MoI&lt;sub>3&lt;/sub> ], at room temperature and a moderately negative potential. A Mo&lt;sup>IV&lt;/sup> nitride species was generated, which is confirmed by electrochemistry and NMR studies. The reaction goes through two successive one electron reductions of the starting Mo species, coordination of a N&lt;sub>2&lt;/sub> molecule, and further splitting to a Mo&lt;sup>IV&lt;/sup> nitride complex. Preliminary DFT studies support the formation of a bridging Mo&lt;sup>I&lt;/sup> N&lt;sub>2&lt;/sub> Mo&lt;sup>I&lt;/sup> dinitrogen dimer evolving to the Mo nitride via a low energy transition state. This example joins a short list of molecular complexes for N&lt;sub>2&lt;/sub> electrochemical reductive cleavage. It opens a door to electrochemical proton-coupled electron transfer (PCET) conversion studies of N&lt;sub>2&lt;/sub> to NH&lt;sub>3&lt;/sub> .</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pagination>e202209899</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9804441</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular Electrochemical Reductive Splitting of Dinitrogen with a Molybdenum Complex.</pubmed_title><pmcid>PMC9804441</pmcid><pubmed_authors>Merakeb L</pubmed_authors><pubmed_authors>De Freitas J</pubmed_authors><pubmed_authors>Bennaamane S</pubmed_authors><pubmed_authors>Clot E</pubmed_authors><pubmed_authors>Mezailles N</pubmed_authors><pubmed_authors>Robert M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular Electrochemical Reductive Splitting of Dinitrogen with a Molybdenum Complex.</name><description>Nitrogen reduction under mild conditions (room T and atmospheric P), using a non-fossil source of hydrogen remains a challenge. Molecular metal complexes, notably Mo based, have recently been shown to be active for such nitrogen fixation. We report electrochemical N&lt;sub>2&lt;/sub> splitting with a Mo&lt;sup>III&lt;/sup> triphosphino complex [(PPP)MoI&lt;sub>3&lt;/sub> ], at room temperature and a moderately negative potential. A Mo&lt;sup>IV&lt;/sup> nitride species was generated, which is confirmed by electrochemistry and NMR studies. The reaction goes through two successive one electron reductions of the starting Mo species, coordination of a N&lt;sub>2&lt;/sub> molecule, and further splitting to a Mo&lt;sup>IV&lt;/sup> nitride complex. Preliminary DFT studies support the formation of a bridging Mo&lt;sup>I&lt;/sup> N&lt;sub>2&lt;/sub> Mo&lt;sup>I&lt;/sup> dinitrogen dimer evolving to the Mo nitride via a low energy transition state. This example joins a short list of molecular complexes for N&lt;sub>2&lt;/sub> electrochemical reductive cleavage. It opens a door to electrochemical proton-coupled electron transfer (PCET) conversion studies of N&lt;sub>2&lt;/sub> to NH&lt;sub>3&lt;/sub> .</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-03-16T08:07:51.115Z</modification><creation>2025-04-05T12:09:52.313Z</creation></dates><accession>S-EPMC9804441</accession><cross_references><pubmed>35941077</pubmed><doi>10.1002/anie.202209899</doi></cross_references></HashMap>