<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(6)</volume><submitter>Lee BYT</submitter><pubmed_abstract>Organometallic Rh(Cp*) (Cp* = η&lt;sup>5&lt;/sup>-pentamethylcyclopentadienyl) complexes with monodentate &lt;i>N&lt;/i>-heterocyclic carbene (NHC) ligands bearing a pendant anthracenyl substituent have been shown to undergo intramolecular C-C coupling reactions. Herein, two bidentate NHC ligands substituted with pyridyl or triazolyl donor groups were prepared along with the corresponding M&lt;sup>II/III&lt;/sup> (M = Ru&lt;sup>II&lt;/sup>, Os&lt;sup>II&lt;/sup>, Rh&lt;sup>III&lt;/sup>, Ir&lt;sup>III&lt;/sup>) complexes. While the Rh(Cp*) complex featuring an NHC-triazole bidentate ligand underwent the equivalent reaction as the monodentate Rh(NHC) complex, &lt;i>i.e.&lt;/i>, it formed a polydentate ligand, the pyridyl-pendant derivative was unequivocally shown to be unreactive. This contrasting behavior was further investigated by dens</pubmed_abstract><journal>ACS organic &amp; inorganic Au</journal><pagination>511-524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9732886</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Triazolyl- vs Pyridyl-Functionalized &lt;i>N&lt;/i>-Heterocyclic Carbene Complexes: Impact of the Pendant N-Donor Ligand on Intramolecular C-C Bond Formation.</pubmed_title><pmcid>PMC9732886</pmcid><pubmed_authors>Phillips AD</pubmed_authors><pubmed_authors>Hartinger CG</pubmed_authors><pubmed_authors>Sohnel T</pubmed_authors><pubmed_authors>Lee BYT</pubmed_authors><pubmed_authors>Hanif M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Triazolyl- vs Pyridyl-Functionalized &lt;i>N&lt;/i>-Heterocyclic Carbene Complexes: Impact of the Pendant N-Donor Ligand on Intramolecular C-C Bond Formation.</name><description>Organometallic Rh(Cp*) (Cp* = η&lt;sup>5&lt;/sup>-pentamethylcyclopentadienyl) complexes with monodentate &lt;i>N&lt;/i>-heterocyclic carbene (NHC) ligands bearing a pendant anthracenyl substituent have been shown to undergo intramolecular C-C coupling reactions. Herein, two bidentate NHC ligands substituted with pyridyl or triazolyl donor groups were prepared along with the corresponding M&lt;sup>II/III&lt;/sup> (M = Ru&lt;sup>II&lt;/sup>, Os&lt;sup>II&lt;/sup>, Rh&lt;sup>III&lt;/sup>, Ir&lt;sup>III&lt;/sup>) complexes. While the Rh(Cp*) complex featuring an NHC-triazole bidentate ligand underwent the equivalent reaction as the monodentate Rh(NHC) complex, &lt;i>i.e.&lt;/i>, it formed a polydentate ligand, the pyridyl-pendant derivative was unequivocally shown to be unreactive. This contrasting behavior was further investigated by dens</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-06T19:39:21.731Z</modification><creation>2024-10-16T19:27:55.969Z</creation></dates><accession>S-EPMC9732886</accession><cross_references><pubmed>36510612</pubmed><doi>10.1021/acsorginorgau.2c00035</doi></cross_references></HashMap>