Ruthenium, rhodium and iridium complexes of the furfuryl-2-(N-diphenylphosphino)methylamine ligand: Molecular structure and catalytic activity
dc.contributor.author | Kayan, Cezmi | |
dc.contributor.author | Meric, Nermin | |
dc.contributor.author | Aydemir, Murat | |
dc.contributor.author | Baysal, Akin | |
dc.contributor.author | Elma, Duygu | |
dc.contributor.author | Ak, Bunyamin | |
dc.contributor.author | Sahin, Ertan | |
dc.date.accessioned | 2024-04-24T16:18:17Z | |
dc.date.available | 2024-04-24T16:18:17Z | |
dc.date.issued | 2012 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | The reaction of furfurylamine with two equivalents of PPh2Cl in the presence of Et3N affords furfuryl-2-(N,N-bis(diphenylphosphino)amine), (Ph2P)(2)NCH2-C4H3O (1). The corresponding ruthenium(II) complex trans-[Ru((PPh2)(2)NCH2-C4H3O)(2)Cl-2] (3) was synthesized by reacting 1 with [Ru(eta(6)-p-cymene)(mu-Cl)Cl](2). The reaction of furfurylamine with one equivalent of PPh2Cl gives Ph2PNHCH2-C4H3O (2). The reaction of 2 with [Ru(eta(6)-p-cymene)(mu-Cl)Cl](2), [Ru(eta(6)-benzene)(mu-Cl)Cl](2), [Rh(mu-Cl)(cod)](2) and [Ir(eta(5)-C5Me5)(mu-Cl)Cl](2) yields the complexes [Ru(Ph2PNHCH2-C4H3S)(eta(6)-p-cymene)Cl-2] (4), [Ru(Ph2PNHCH2-C4H3O)(eta(6-)benzene)Cl-2] (5), [Rh(Pb2PNHCH2-C4H3O)(cod)Cl] (6) and [Ir(Ph2PNHCH2-C4H3O)(eta(5)-C5Me5)Cl-2] (7), respectively. All the complexes were isolated from the reaction solution and fully characterized by analytical and spectroscopic methods. The structure of [Ru(Ph2PNHCH2-C4H3O)(eta(6)-p-cymene)Cl-2] (4) was also determined by single crystal X-ray diffraction. Complexes 3-7 are suitable precursors forming highly active catalysts in the transfer hydrogenation of a variety of simple ketones. Notably, the catalysts obtained by using the ruthenium complexes [Ru(Ph2PNHCH2-C4H3O)(eta(6)-p-cymene)Cl-2] (4) and [Ru(Ph2PNHCH2-C4H3O)(eta(6)-benzene)Cl-2] (5) are much more active in the transfer hydrogenation, converting the carbonyls to the corresponding alcohols in 97-99% yields (TOF <= 300 h(-1)), compared to analogous rhodium and iridium complexes and the trans-Ru(II)-p-cymene bis(phosphino)amine complex. (c) 2012 Elsevier Ltd. All rights reserved. | en_US |
dc.identifier.doi | 10.1016/j.poly.2012.05.009 | |
dc.identifier.endpage | 148 | en_US |
dc.identifier.issn | 0277-5387 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.scopus | 2-s2.0-84863785050 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 142 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.poly.2012.05.009 | |
dc.identifier.uri | https://hdl.handle.net/11468/15959 | |
dc.identifier.volume | 42 | en_US |
dc.identifier.wos | WOS:000307152900020 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | en_US |
dc.publisher | Pergamon-Elsevier Science Ltd | en_US |
dc.relation.ispartof | Polyhedron | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Aminophosphine | en_US |
dc.subject | Transfer Hydrogenation | en_US |
dc.subject | Ruthenium | en_US |
dc.subject | Rhodium | en_US |
dc.subject | Iridium | en_US |
dc.subject | X-Ray Diffraction | en_US |
dc.title | Ruthenium, rhodium and iridium complexes of the furfuryl-2-(N-diphenylphosphino)methylamine ligand: Molecular structure and catalytic activity | en_US |
dc.title | Ruthenium, rhodium and iridium complexes of the furfuryl-2-(N-diphenylphosphino)methylamine ligand: Molecular structure and catalytic activity | |
dc.type | Article | en_US |