Hexacoordinated tin complexes catalyse imine hydrogenation with H

• Published in: Chemical communications (Cambridge, England) Vol. 6; no. 24; pp. 3287 - 329
• Main Authors: áková, Andrea, Saha, Pritha, Paparakis, Alexandros, Zábranský, Martin, Gastelu, Gabriela, Kukla, Jaroslav, Uranga, Jorge G, Hulla, Martin
• Format: Journal Article
• Published: 19.03.2024
• ISSN: 1359-7345; 1364-548X
• DOI: 10.1039/d3cc05878f

Frustrated Lewis pair (FLP) hydrogenation catalysts predominantly use alkyl- and aryl-substituted Lewis acids (LA) that offer a limited number of combinations of substituents, limiting our ability to tune their properties and, ultimately, their reactivity. Nevertheless, main-group complexes have numerous ligands available for such purposes, which could enable us to broaden the range of FLP catalysis. Supporting this hypothesis, we demonstrate here that hexacoordinated tin complexes with Schiff base ligands catalyse imine hydrogenation via activation of H 2(g) . As shown by hydrogen-deuterium scrambling, [Sn( t Bu 2 Salen)(OTf) 2 ] activated H 2(g) at 25 °C and 10 bar of H 2 . After tuning the ligands, we found that [Sn(Salen)Cl 2 ] was the most efficient imine hydrogenation catalyst despite having the lowest activity in H 2(g) activation. Moreover, various imines were hydrogenated in yields up to 98% thereby opening up opportunities for developing novel FLP hydrogenation catalysts based on hexacoordinated LA of main-group elements. Main group complexes of tin( iv ) with Schiff base ligands activate H 2 and act as hydrogenation catalysts.