<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6</volume><submitter>Wu F</submitter><pubmed_abstract>The ability to modulate the spin states of adsorbed molecules is in high demand for molecular spintronics applications. Here, we demonstrate that the spin state of a corrole complex can be tuned by expanding its fused ring as a result of the modification to the d-π interaction between the metal and ligand. A bicyclo[2.2.2]octadiene-fused copper corrole can readily be converted into a tetrabenzocorrole radical on an Au(111) substrate during the sublimation process. In the scanning tunnelling spectroscopy spectrum, a sharp Kondo resonance appears near the Fermi level on the corrole ligand of the tetrabenzocorrole molecule. In contrast, a non-fused-ring-expanded copper corrole molecule, copper 5,10,15-triphenylcorrole, shows no such Kondo feature. Mapping of the Kondo resonance demonstrates t</pubmed_abstract><journal>Nature communications</journal><pagination>7547</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4491828</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Modulation of the molecular spintronic properties of adsorbed copper corroles.</pubmed_title><pmcid>PMC4491828</pmcid><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Shen Z</pubmed_authors><pubmed_authors>Mishra P</pubmed_authors><pubmed_authors>Komeda T</pubmed_authors><pubmed_authors>Mack J</pubmed_authors><pubmed_authors>Wu F</pubmed_authors><pubmed_authors>Chang Y</pubmed_authors><pubmed_authors>Kobayashi N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Modulation of the molecular spintronic properties of adsorbed copper corroles.</name><description>The ability to modulate the spin states of adsorbed molecules is in high demand for molecular spintronics applications. Here, we demonstrate that the spin state of a corrole complex can be tuned by expanding its fused ring as a result of the modification to the d-π interaction between the metal and ligand. A bicyclo[2.2.2]octadiene-fused copper corrole can readily be converted into a tetrabenzocorrole radical on an Au(111) substrate during the sublimation process. In the scanning tunnelling spectroscopy spectrum, a sharp Kondo resonance appears near the Fermi level on the corrole ligand of the tetrabenzocorrole molecule. In contrast, a non-fused-ring-expanded copper corrole molecule, copper 5,10,15-triphenylcorrole, shows no such Kondo feature. Mapping of the Kondo resonance demonstrates t</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2025-04-04T11:06:42.744Z</modification><creation>2019-03-27T01:54:34Z</creation></dates><accession>S-EPMC4491828</accession><cross_references><pubmed>26112968</pubmed><doi>10.1038/ncomms8547</doi></cross_references></HashMap>