<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nikol AT</submitter><funding>Carlsbergfondet</funding><funding>Danmarks Frie Forskningsfond</funding><funding>Villum Fonden</funding><funding>Novo Nordisk Fonden</funding><pagination>26209</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11527872</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(1)</volume><pubmed_abstract>Formic acid is one of the most promising candidates for the long-term storage of hydrogen in liquid form. Herein, we present a new collection of ruthenium pincer complexes of the general formula [RuHCl(POP)(PPh&lt;sub>3&lt;/sub>)] using commercially available or easy-to-synthesize tridentate xantphos-type POP pincer ligands. We applied these complexes in the dehydrogenation of formic acid to CO&lt;sub>2&lt;/sub> and H&lt;sub>2&lt;/sub> using the ionic liquid BMIM OAc (1-butyl-3-methylimidazolium acetate) as solvent under mild, reflux-free conditions. The best performing catalyst with respect to maximum turnover frequency, the literature-known complex [RuHCl(xantphos)(PPh&lt;sub>3&lt;/sub>)] Ru-1, produced a maximum turnover frequency of 4525 h&lt;sup>-1&lt;/sup> with 74% conversion after 10 min at 90 °C and complete conversion (> 98%) occurring within 3 h. On the other hand, the best overall performing catalyst, the novel complex [RuHCl(iPr-dbfphos)(PPh&lt;sub>3&lt;/sub>)] Ru-2, facilitated full conversion within 1 h leading to an overall turnover frequency of 1009 h&lt;sup>-1&lt;/sup>. Moreover, catalytic activity was observed at temperatures as low as 60 °C. Only CO&lt;sub>2&lt;/sub> and H&lt;sub>2&lt;/sub> are observed in the gas phase, with no CO detected. High-resolution mass spectrometry suggests the presence of N-heterocyclic carbene complexes in the reaction mixture.</pubmed_abstract><journal>Scientific reports</journal><pubmed_title>Formic acid dehydrogenation using Ruthenium-POP pincer complexes in ionic liquids.</pubmed_title><pmcid>PMC11527872</pmcid><funding_grant_id>19049</funding_grant_id><funding_grant_id>1127-00172B</funding_grant_id><funding_grant_id>CF20-0365</funding_grant_id><funding_grant_id>NNF20OC0064560</funding_grant_id><pubmed_authors>Nikol AT</pubmed_authors><pubmed_authors>Jorgensen MSB</pubmed_authors><pubmed_authors>Rabell B</pubmed_authors><pubmed_authors>Nielsen M</pubmed_authors><pubmed_authors>Larsen RW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Formic acid dehydrogenation using Ruthenium-POP pincer complexes in ionic liquids.</name><description>Formic acid is one of the most promising candidates for the long-term storage of hydrogen in liquid form. Herein, we present a new collection of ruthenium pincer complexes of the general formula [RuHCl(POP)(PPh&lt;sub>3&lt;/sub>)] using commercially available or easy-to-synthesize tridentate xantphos-type POP pincer ligands. We applied these complexes in the dehydrogenation of formic acid to CO&lt;sub>2&lt;/sub> and H&lt;sub>2&lt;/sub> using the ionic liquid BMIM OAc (1-butyl-3-methylimidazolium acetate) as solvent under mild, reflux-free conditions. The best performing catalyst with respect to maximum turnover frequency, the literature-known complex [RuHCl(xantphos)(PPh&lt;sub>3&lt;/sub>)] Ru-1, produced a maximum turnover frequency of 4525 h&lt;sup>-1&lt;/sup> with 74% conversion after 10 min at 90 °C and complete conversion (> 98%) occurring within 3 h. On the other hand, the best overall performing catalyst, the novel complex [RuHCl(iPr-dbfphos)(PPh&lt;sub>3&lt;/sub>)] Ru-2, facilitated full conversion within 1 h leading to an overall turnover frequency of 1009 h&lt;sup>-1&lt;/sup>. Moreover, catalytic activity was observed at temperatures as low as 60 °C. Only CO&lt;sub>2&lt;/sub> and H&lt;sub>2&lt;/sub> are observed in the gas phase, with no CO detected. High-resolution mass spectrometry suggests the presence of N-heterocyclic carbene complexes in the reaction mixture.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-05T09:14:19.924Z</modification><creation>2025-04-05T09:14:19.924Z</creation></dates><accession>S-EPMC11527872</accession><cross_references><pubmed>39482323</pubmed><doi>10.1038/s41598-024-76782-3</doi></cross_references></HashMap>