<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Back N</submitter><funding>Oklahoma Center for the Advancement of Science and Technology</funding><pagination>2087-2101</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12809709</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(4)</volume><pubmed_abstract>CO&lt;sub>2&lt;/sub> utilization is a significant and emerging field in catalysis, playing a crucial role in reducing atmospheric CO&lt;sub>2&lt;/sub> and mitigating climate change. In this work, we report on Cu(i) complexes that utilize atmospheric CO&lt;sub>2&lt;/sub> for the direct carboxylation and esterification of terminal alkynes. The Cu(i) complexes bear ligands of the type 2,6-bis(3-alkyl/arylimidazol-2-ylidene) methylpyridine I(R)&lt;sup>C^N^C&lt;/sup>, where R = &lt;sup>i&lt;/sup>Pr, Me, 2,6-&lt;sup>i&lt;/sup>Pr&lt;sub>2&lt;/sub>Ph (Dipp), 2,4,6-Me&lt;sub>3&lt;/sub>Ph (Mes), and 4-CF&lt;sub>3&lt;/sub>Ph. While copper-catalyzed carboxylation reactions are not unprecedented, this work presents the first example of metal ligand cooperativity (MLC) through a dearomatization-aromatization process used in the direct carboxylation of term</pubmed_abstract><journal>Chemical science</journal><pubmed_title>Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.</pubmed_title><pmcid>PMC12809709</pmcid><funding_grant_id>HR23-008</funding_grant_id><pubmed_authors>Back N</pubmed_authors><pubmed_authors>Guthrie E</pubmed_authors><pubmed_authors>de Visser SP</pubmed_authors><pubmed_authors>Zhu C</pubmed_authors><pubmed_authors>Tahsini L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Metal ligand cooperativity in the direct carboxylation and esterification of terminal alkynes by Cu-CNC complexes bearing 2,6-lutidine linkers.</name><description>CO&lt;sub>2&lt;/sub> utilization is a significant and emerging field in catalysis, playing a crucial role in reducing atmospheric CO&lt;sub>2&lt;/sub> and mitigating climate change. In this work, we report on Cu(i) complexes that utilize atmospheric CO&lt;sub>2&lt;/sub> for the direct carboxylation and esterification of terminal alkynes. The Cu(i) complexes bear ligands of the type 2,6-bis(3-alkyl/arylimidazol-2-ylidene) methylpyridine I(R)&lt;sup>C^N^C&lt;/sup>, where R = &lt;sup>i&lt;/sup>Pr, Me, 2,6-&lt;sup>i&lt;/sup>Pr&lt;sub>2&lt;/sub>Ph (Dipp), 2,4,6-Me&lt;sub>3&lt;/sub>Ph (Mes), and 4-CF&lt;sub>3&lt;/sub>Ph. While copper-catalyzed carboxylation reactions are not unprecedented, this work presents the first example of metal ligand cooperativity (MLC) through a dearomatization-aromatization process used in the direct carboxylation of term</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-06-11T05:57:56.799Z</modification><creation>2026-06-11T03:12:14.322Z</creation></dates><accession>S-EPMC12809709</accession><cross_references><pubmed>41550563</pubmed><doi>10.1039/d5sc08379f</doi></cross_references></HashMap>