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               <dc:title>Ruthenium complexes of P-stereogenic phosphines with a heterocyclic substituent</dc:title>
               <dc:creator>Clavero Puyal, Pau</dc:creator>
               <dc:creator>Grabulosa, Arnald</dc:creator>
               <dc:creator>Rocamora Mercè, Mercè</dc:creator>
               <dc:creator>Muller, G.</dc:creator>
               <dc:creator>Font Bardia, Ma. Mercedes</dc:creator>
               <dc:subject>Ruteni</dc:subject>
               <dc:subject>Catàlisi asimètrica</dc:subject>
               <dc:subject>Quiralitat</dc:subject>
               <dc:subject>Ruthenium</dc:subject>
               <dc:subject>Enantioselective catalysis</dc:subject>
               <dc:subject>Chirality</dc:subject>
               <dc:description>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.</dc:description>
               <dc:date>2020-06-02T11:01:20Z</dc:date>
               <dc:date>2020-06-02T11:01:20Z</dc:date>
               <dc:date>2016-04-12</dc:date>
               <dc:date>2020-06-02T11:01:20Z</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:type>info:eu-repo/semantics/acceptedVersion</dc:type>
               <dc:relation>Versió postprint del document publicat a: https://doi.org/10.1039/c6dt00995f</dc:relation>
               <dc:relation>Dalton Transactions, 2016, vol. 45, num. 20, p. 8513-8531</dc:relation>
               <dc:relation>https://doi.org/10.1039/c6dt00995f</dc:relation>
               <dc:rights>(c) Clavero Puyal, Pau et al., 2016</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:publisher>Royal Society of Chemistry</dc:publisher>
               <dc:source>Articles publicats en revistes (Mineralogia, Petrologia i Geologia Aplicada)</dc:source>
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