2026-04-17T14:42:46Zhttps://recercat.cat/oai/requestoai:recercat.cat:2445/1637202025-11-19T10:54:19Zcom_2072_1057col_2072_478917col_2072_478923
RECERCAT
author
Clavero Puyal, Pau
author
Grabulosa, Arnald
author
Rocamora Mercè, Mercè
author
Muller, G.
author
Font Bardia, Ma. Mercedes
2020-06-02T11:01:20Z2020-06-02T11:01:20Z2016-04-122020-06-02T11:01:20Z
The synthesis via phosphine-boranes of 13 new optically pure P-stereogenic diarylphosphines P(Het)PhR (Het = 4-dibenzofuranyl (DBF), 4-dibenzothiophenyl (DBT), 4-dibenzothiophenyl-S,S-dioxide (DBTO2) and 1-thianthrenyl (TA); R = OMe, Me, i-Pr, Fc (ferrocenyl)) following the Jugé-Stephan method is described. The ligands were designed with the aim of having a heteroatom in a position capable of interacting with a metal upon coordination. The ligands and their precursors have been fully characterised, including the determination of two crystal structures of phosphine-boranes. Ru neutral complexes of the type [RuCl2(η6-arene)(κP-P)] (arene = p-cymene and methyl benzoate) have been prepared and characterised, including three crystal structure determinations. Treatment of solutions of the complexes with TlPF6 allowed the preparation of well-defined cationic complexes [RuCl(η6-arene)(κ2P,S-P)]PF6 for DBT- and TA-based phosphines. The complexes possess a stereogenic Ru atom and in most of the cases they are present as a single isomer in solution. All the Ru complexes have been used in the asymmetric transfer hydrogenation of acetophenone in refluxing 2-propanol, with good activities and up to 70% ee.
(c) Clavero Puyal, Pau et al., 2016 info:eu-repo/semantics/openAccess
Ruteni
Catàlisi asimètrica
Quiralitat
Ruthenium
Enantioselective catalysis
Chirality
Ruthenium complexes of P-stereogenic phosphines with a heterocyclic substituent
info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion