Introducing the perfluorinated Cp* ligand into coordination chemistry

Abstract: The reaction of AgBF4 and [Rh(COD)Cl]2 (COD=1,5-cyclooctadiene) in presence of [NEt4][C5(CF3)5] afforded the fluorocarbon soluble complex [Rh(COD)(C5(CF3)5)] by salt metathesis. This complex represents the first example for a successful coordination of the weakly basic [C5(CF3)5]− ligand, since its first synthesis in 1980. In addition to [Rh(COD)(C5(CF3)5)] also the byproduct [Rh(COD)(C5(CF3)4H)] was isolated and fully characterized. Accompanying DFT studies showed that the interaction energy of the [C5(CF3)5]− ligand towards the 12-electron fragment [Rh(COD)]+ is ≈70 kcal mol−1 lower in comparison to [C5(CH3)5]− due to reduced electrostatic interactions and weaker π-donor properties of the ligand. The quantitative but reversible substitution of the [C5(CF3)5]− ligand by toluene, converting it into a weakly coordinating anion, experimentally proved the extraordinary weak bonding interaction

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch
Anmerkungen
Angewandte Chemie. International edition. - 61, 43 (2022) , e202211147, ISSN: 1521-3773

Ereignis
Veröffentlichung
(wo)
Freiburg
(wer)
Universität
(wann)
2022
Urheber
Sievers, Robin
Sellin, Malte
Rupf, Susanne M.
Parche, Joshua
Malischewski, Moritz

DOI
10.1002/anie.202211147
URN
urn:nbn:de:bsz:25-freidok-2314471
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
25.03.2025, 13:46 MEZ

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