Ketone hydrogenation catalyzed by a new iron(ii)–PNN complex. Issue 12 (15th February 2016)

• Record Type: Journal Article
• Authors: Butschke, B.; Feller, M.; Diskin-Posner, Y.; Milstein, D.
• Is Part Of: Catalysis science & technology. Volume 6:Issue 12(2016)
• Page Start: 4428
• Page End: 4437
• Publication Date: 2016-02-15
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/c5cy02036k
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : A dearomatized Fe(ii )–hydride complex mediates the hydrogenation of enolizable ketones under very mild conditions. Deactivation occurs via intramolecular proton migration. Abstract : The formal Fe II –hydride complex [Fe(H)(CO)(MeCN)LPNN ](BF4 ) (1 ) (LPNN = 2-[(di- tert -butylphosphino)methyl]-6-[1-(mesitylimino)ethyl]pyridine) catalyzes the hydrogenation of ketones under mild conditions (room temperature, p (H2 ) = 4 bar) and short reaction times (1–3 h) in the presence of catalytic amounts of KHMDS as a base. The reaction presumably proceeds via a dearomatization/rearomatization mechanism. However, in comparison with the reaction of related iron–PNP complexes, the reaction mechanism seems to be different, and an enolate formation step appears to precede catalysis. Moreover, the catalytic performance of the PNN system is inferior under similar conditions, and this observation is probably a consequence of an intramolecular deactivation pathway, which involves reductive proton migration within a dearomatized Fe II –hydride complex to form a catalytically inactive Fe 0 species. The weaker electron-donating properties of the PNN ligand system, when compared with analogous PNP-based ligands, cause the dearomatized PNN iron(ii )–hydride intermediate to be less electron-rich and consequently more prone to the intramolecular reductive elimination pathway. This result is in line with the need for electron-rich metal hydrides for efficient hydrogenation catalysis to take place.