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An Anionic Dinuclear Ruthenium Dihydrogen Complex of Relevance for Alkyne gem‐Hydrogenation

During an investigation into the fate of ruthenium precatalysts used for light‐driven alkyne gem‐hydrogenation reactions with formation of Grubbs‐type ruthenium catalysts, it was found that the reaction of [(IPr)(η(6)‐cymene)RuCl(2)] with H(2) under UV‐irradiation affords an anionic dinuclear σ‐dihy...

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Detalles Bibliográficos
Autores principales: Biberger, Tobias, Nöthling, Nils, Leutzsch, Markus, Gordon, Christopher P., Copéret, Christophe, Fürstner, Alois
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322539/
https://www.ncbi.nlm.nih.gov/pubmed/35363926
http://dx.doi.org/10.1002/anie.202201311
Descripción
Sumario:During an investigation into the fate of ruthenium precatalysts used for light‐driven alkyne gem‐hydrogenation reactions with formation of Grubbs‐type ruthenium catalysts, it was found that the reaction of [(IPr)(η(6)‐cymene)RuCl(2)] with H(2) under UV‐irradiation affords an anionic dinuclear σ‐dihydrogen complex, which is thermally surprisingly robust. Not only are anionic σ‐complexes in general exceedingly rare, but the newly formed species seems to be the first example lacking any structural attributes able to counterbalance the negative charge and, in so doing, prevent oxidative insertion of the metal centers into the ligated H(2) from occurring.