<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(1)</volume><submitter>Zhang Y</submitter><pubmed_abstract>The structurally precise alloy nanoclusters have been emerged as a burgeoning nanomaterial for their unique physical/chemical features. We here report a rod-like nanocluster [Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>10&lt;/sub>I&lt;sub>7&lt;/sub>](SbF&lt;sub>6&lt;/sub>)&lt;sub>2&lt;/sub> (Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub>), which was generated through a transformation of a [Au&lt;sub>9&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>8&lt;/sub>]&lt;sup>3+&lt;/sup> intermediate in the presence of CuI, unveiled by time-dependent UV-vis spectroscopy, electrospray ionization mass spectrometry as well as single crystal X-ray diffraction. Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub> is comprised of two pentagonal bipyramids Au&lt;sub>6&lt;/sub>Cu units and a pentagonal prism Cu&lt;sub>11&lt;/sub> unit, where the copper and gold species are presented in +1 and 0 chemical states. The Cu-dopants significantly improved the stability and fluorescence (quantum yield: ~34%, 34-folds of homo-Au&lt;sub>25&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>10&lt;/sub>Br&lt;sub>7&lt;/sub>). The high stability of Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub> is attributed to the high binding energy of iodine ligands, Au-Cu synergistic effects and its 16-electon system as an 8-electron superatom dimer. Finally, the robust Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub> exhibited high catalytic activity (~92% conversion and ~84% methyl formate-selectivity) and good durability in methanol photo-oxidation.</pubmed_abstract><journal>Communications chemistry</journal><pagination>24</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9908894</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Atomically precise copper dopants in metal clusters boost up stability, fluorescence, and photocatalytic activity.</pubmed_title><pmcid>PMC9908894</pmcid><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Sharma S</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Qin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Atomically precise copper dopants in metal clusters boost up stability, fluorescence, and photocatalytic activity.</name><description>The structurally precise alloy nanoclusters have been emerged as a burgeoning nanomaterial for their unique physical/chemical features. We here report a rod-like nanocluster [Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>10&lt;/sub>I&lt;sub>7&lt;/sub>](SbF&lt;sub>6&lt;/sub>)&lt;sub>2&lt;/sub> (Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub>), which was generated through a transformation of a [Au&lt;sub>9&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>8&lt;/sub>]&lt;sup>3+&lt;/sup> intermediate in the presence of CuI, unveiled by time-dependent UV-vis spectroscopy, electrospray ionization mass spectrometry as well as single crystal X-ray diffraction. Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub> is comprised of two pentagonal bipyramids Au&lt;sub>6&lt;/sub>Cu units and a pentagonal prism Cu&lt;sub>11&lt;/sub> unit, where the copper and gold species are presented in +1 and 0 chemical states. The Cu-dopants significantly improved the stability and fluorescence (quantum yield: ~34%, 34-folds of homo-Au&lt;sub>25&lt;/sub>(PPh&lt;sub>3&lt;/sub>)&lt;sub>10&lt;/sub>Br&lt;sub>7&lt;/sub>). The high stability of Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub> is attributed to the high binding energy of iodine ligands, Au-Cu synergistic effects and its 16-electon system as an 8-electron superatom dimer. Finally, the robust Au&lt;sub>12&lt;/sub>Cu&lt;sub>13&lt;/sub> exhibited high catalytic activity (~92% conversion and ~84% methyl formate-selectivity) and good durability in methanol photo-oxidation.</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-04T18:43:18.136Z</modification><creation>2025-04-04T18:43:18.136Z</creation></dates><accession>S-EPMC9908894</accession><cross_references><pubmed>36755056</pubmed><doi>10.1038/s42004-023-00817-5</doi></cross_references></HashMap>