Exploring the stability of the NHC-metal bond using thiones as probes
The metal-carbon bond in N-heterocyclic carbene (NHC) metal complexes, which are ubiquitous in modern homogeneous catalysis, is often conjectured to be robust. Here, carbene dissociation was evaluated from a series of complexes with metals of relevance in catalysis containing either an Arduengo-type...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2021-10, Vol.57 (81), p.16-163 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The metal-carbon bond in N-heterocyclic carbene (NHC) metal complexes, which are ubiquitous in modern homogeneous catalysis, is often conjectured to be robust. Here, carbene dissociation was evaluated from a series of complexes with metals of relevance in catalysis containing either an Arduengo-type 2-imidazolylidene or a mesoionic 1,2,3-triazolylidene ligand through thione formation, revealing remarkable kinetic lability of the NHC-metal bond for,
e.g.
Ir
III
, Rh
III
, and Ni
II
complexes.
The stability of Arduengo-type N-heterocyclic carbenes and mesoionic triazolylidenes to a range of catalytically active metals was probed. Remarkably labile bonding was observed with some metals, which impacts mechanistic considerations in catalysis. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/d1cc02740a |