Ruthenium, rhodium and iridium complexes of the furfuryl-2-(N-diphenylphosphino)methylamine ligand: Molecular structure and catalytic activity

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dc.authoridKayan, Cezmi/0000-0001-5700-8546
dc.authoridGurbuz, Nevin/0000-0003-3201-3597
dc.authoridÖzdemir, İsmail/0000-0001-6325-0216
dc.authoridAydemir, Murat/0000-0002-4238-5012
dc.authoridBaysal, Akin/0000-0001-7294-6792
dc.authorwosidKarakaş, duygu Elma/ABE-4017-2020
dc.authorwosidKayan, Cezmi/AAC-1876-2021
dc.authorwosidGurbuz, Nevin/A-3069-2016
dc.authorwosidmeric, nermin/AAT-9164-2021
dc.authorwosidÖzdemir, İsmail/ABI-5192-2020
dc.authorwosidBaysal, Akin/I-6378-2018
dc.contributor.authorKayan, Cezmi
dc.contributor.authorMeric, Nermin
dc.contributor.authorAydemir, Murat
dc.contributor.authorBaysal, Akin
dc.contributor.authorElma, Duygu
dc.contributor.authorAk, Bunyamin
dc.contributor.authorSahin, Ertan
dc.date.accessioned2024-08-04T20:36:00Z
dc.date.available2024-08-04T20:36:00Z
dc.date.issued2012
dc.departmentİnönü Üniversitesien_US
dc.description.abstractThe 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.doi10.1016/j.poly.2012.05.009
dc.identifier.endpage148en_US
dc.identifier.issn0277-5387
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-84863785050en_US
dc.identifier.scopusqualityQ2en_US
dc.identifier.startpage142en_US
dc.identifier.urihttps://doi.org/10.1016/j.poly.2012.05.009
dc.identifier.urihttps://hdl.handle.net/11616/95719
dc.identifier.volume42en_US
dc.identifier.wosWOS:000307152900020en_US
dc.identifier.wosqualityQ2en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofPolyhedronen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAminophosphineen_US
dc.subjectTransfer hydrogenationen_US
dc.subjectRutheniumen_US
dc.subjectRhodiumen_US
dc.subjectIridiumen_US
dc.subjectX-ray diffractionen_US
dc.titleRuthenium, rhodium and iridium complexes of the furfuryl-2-(N-diphenylphosphino)methylamine ligand: Molecular structure and catalytic activityen_US
dc.typeArticleen_US

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