<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>62(4)</volume><submitter>Bevilacqua M</submitter><funding>Dipartimento di Scienze Chimiche, Universit? di Padova</funding><funding>Consorzio Interuniversitario per le Reattivit? Chimiche e la Catalisi</funding><pubmed_abstract>Herein, we report a new method to synthesize molecular gold nanoclusters (AuNCs) stabilized by phosphine (PR&lt;sub>3&lt;/sub>) and di-N-heterocyclic carbene (di-NHC) ligands. The interaction of di-NHC gold(I) complexes, with the general formula [(di-NHC)Au&lt;sub>2&lt;/sub>Cl&lt;sub>2&lt;/sub>] with well-known [Au&lt;sub>11&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>8&lt;/sub>Cl&lt;sub>2&lt;/sub>]Cl clusters provides three new classes of AuNCs through a controllable reaction sequence. The synthesis involves an initial ligand metathesis reaction to produce [Au&lt;sub>11&lt;/sub>(di-NHC)(PPh&lt;sub>3&lt;/sub>)&lt;sub>6&lt;/sub>Cl&lt;sub>2&lt;/sub>]&lt;sup>+&lt;/sup> (type &lt;b>1&lt;/b> clusters), followed by a thermally induced rearrangement/metal complex addition with the formation of Au&lt;sub>13&lt;/sub> clusters [Au&lt;sub>13&lt;/sub>(di-NHC)&lt;sub>2&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>4&lt;/sub>Cl&lt;sub>4&lt;/sub>]&lt;sup>+&lt;/sup> (type &lt;b>2&lt;/b> clusters). Finally, an additional metathesis process yields [Au&lt;sub>13&lt;/sub>(di-NHC)&lt;sub>3&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>3&lt;/sub>Cl&lt;sub>3&lt;/sub>]&lt;sup>2+&lt;/sup> (type &lt;b>3&lt;/b> clusters). The electronic and steric properties of the employed di-NHC ligand affect the product distribution, leading to the isolation and full characterization of different clusters as the main product. A type &lt;b>3&lt;/b> cluster has been also structurally characterized and was preliminarily found to be strongly emissive in solution.</pubmed_abstract><journal>Inorganic chemistry</journal><pagination>1383-1393</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9890486</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>From Au&lt;sub>11&lt;/sub> to Au&lt;sub>13&lt;/sub>: Tailored Synthesis of Superatomic Di-NHC/PPh&lt;sub>3&lt;/sub>-Stabilized Molecular Gold Nanoclusters.</pubmed_title><pmcid>PMC9890486</pmcid><pubmed_authors>Graiff C</pubmed_authors><pubmed_authors>Bogialli S</pubmed_authors><pubmed_authors>Biffis A</pubmed_authors><pubmed_authors>Roverso M</pubmed_authors><pubmed_authors>Bevilacqua M</pubmed_authors></additional><is_claimable>false</is_claimable><name>From Au&lt;sub>11&lt;/sub> to Au&lt;sub>13&lt;/sub>: Tailored Synthesis of Superatomic Di-NHC/PPh&lt;sub>3&lt;/sub>-Stabilized Molecular Gold Nanoclusters.</name><description>Herein, we report a new method to synthesize molecular gold nanoclusters (AuNCs) stabilized by phosphine (PR&lt;sub>3&lt;/sub>) and di-N-heterocyclic carbene (di-NHC) ligands. The interaction of di-NHC gold(I) complexes, with the general formula [(di-NHC)Au&lt;sub>2&lt;/sub>Cl&lt;sub>2&lt;/sub>] with well-known [Au&lt;sub>11&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>8&lt;/sub>Cl&lt;sub>2&lt;/sub>]Cl clusters provides three new classes of AuNCs through a controllable reaction sequence. The synthesis involves an initial ligand metathesis reaction to produce [Au&lt;sub>11&lt;/sub>(di-NHC)(PPh&lt;sub>3&lt;/sub>)&lt;sub>6&lt;/sub>Cl&lt;sub>2&lt;/sub>]&lt;sup>+&lt;/sup> (type &lt;b>1&lt;/b> clusters), followed by a thermally induced rearrangement/metal complex addition with the formation of Au&lt;sub>13&lt;/sub> clusters [Au&lt;sub>13&lt;/sub>(di-NHC)&lt;sub>2&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>4&lt;/sub>Cl&lt;sub>4&lt;/sub>]&lt;sup>+&lt;/sup> (type &lt;b>2&lt;/b> clusters). Finally, an additional metathesis process yields [Au&lt;sub>13&lt;/sub>(di-NHC)&lt;sub>3&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>3&lt;/sub>Cl&lt;sub>3&lt;/sub>]&lt;sup>2+&lt;/sup> (type &lt;b>3&lt;/b> clusters). The electronic and steric properties of the employed di-NHC ligand affect the product distribution, leading to the isolation and full characterization of different clusters as the main product. A type &lt;b>3&lt;/b> cluster has been also structurally characterized and was preliminarily found to be strongly emissive in solution.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2026-06-18T08:45:08.204Z</modification><creation>2025-04-06T15:43:33.616Z</creation></dates><accession>S-EPMC9890486</accession><cross_references><pubmed>36638827</pubmed><doi>10.1021/acs.inorgchem.2c03331</doi></cross_references></HashMap>