<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sievers R</submitter><funding>DFG Deutsche Forschungsgemeinschaft</funding><pagination>e202211147</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9826324</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>61(43)</volume><pubmed_abstract>The reaction of AgBF&lt;sub>4&lt;/sub> and [Rh(COD)Cl]&lt;sub>2&lt;/sub> (COD=1,5-cyclooctadiene) in presence of [NEt&lt;sub>4&lt;/sub> ][C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> ] afforded the fluorocarbon soluble complex [Rh(COD)(C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> )] by salt metathesis. This complex represents the first example for a successful coordination of the weakly basic [C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> ]&lt;sup>-&lt;/sup> ligand, since its first synthesis in 1980. In addition to [Rh(COD)(C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> )] also the byproduct [Rh(COD)(C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>4&lt;/sub> H)] was isolated and fully characterized. Accompanying DFT studies showed that the interaction energy of the [C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> ]&lt;sup>-&lt;/sup> ligand towa</pubmed_abstract><journal>Angewandte Chemie (International ed. in English)</journal><pubmed_title>Introducing the Perfluorinated Cp* Ligand into Coordination Chemistry.</pubmed_title><pmcid>PMC9826324</pmcid><funding_grant_id>387284271 - SFB 1349</funding_grant_id><pubmed_authors>Sievers R</pubmed_authors><pubmed_authors>Malischewski M</pubmed_authors><pubmed_authors>Sellin M</pubmed_authors><pubmed_authors>Rupf SM</pubmed_authors><pubmed_authors>Parche J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Introducing the Perfluorinated Cp* Ligand into Coordination Chemistry.</name><description>The reaction of AgBF&lt;sub>4&lt;/sub> and [Rh(COD)Cl]&lt;sub>2&lt;/sub> (COD=1,5-cyclooctadiene) in presence of [NEt&lt;sub>4&lt;/sub> ][C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> ] afforded the fluorocarbon soluble complex [Rh(COD)(C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> )] by salt metathesis. This complex represents the first example for a successful coordination of the weakly basic [C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> ]&lt;sup>-&lt;/sup> ligand, since its first synthesis in 1980. In addition to [Rh(COD)(C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> )] also the byproduct [Rh(COD)(C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>4&lt;/sub> H)] was isolated and fully characterized. Accompanying DFT studies showed that the interaction energy of the [C&lt;sub>5&lt;/sub> (CF&lt;sub>3&lt;/sub> )&lt;sub>5&lt;/sub> ]&lt;sup>-&lt;/sup> ligand towa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-03-27T15:40:14.293Z</modification><creation>2025-02-18T23:35:38.05Z</creation></dates><accession>S-EPMC9826324</accession><cross_references><pubmed>35984742</pubmed><doi>10.1002/anie.202211147</doi></cross_references></HashMap>