Applications of transition metal complexes containing aminophosphine ligand to transfer hydrogenation of ketones
dc.contributor.author | Aydemir, Murat | |
dc.contributor.author | Baysal, Akın | |
dc.contributor.author | Turgut, Yılmaz | |
dc.contributor.orcid | 0000-0001-7294-6792 | |
dc.date.accessioned | 2024-04-24T15:59:18Z | |
dc.date.available | 2024-04-24T15:59:18Z | |
dc.date.issued | 2011 | |
dc.department | Dicle Üniversitesi, Fen Fakültesi, Kimya Bölümü | en_US |
dc.description.abstract | Hydrogen transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity. Reaction of [Ph2PNHCH2-C4H3S] with [Ru(eta(6)-benzene)(mu-Cl)Cl](2), [Rh(mu-Cl)(cod)](2) and [Ir(eta(5)-C5Me5)(mu-Cl)Cl](2) gave a range of new monodendate complexes [Ru(Ph2PNHCH2-C4H3S)(eta(6)-benzene)Cl-2], 1, [Rh(Ph2PNHCH2-C4H3S)(cod)Cl], 2, and [Ir(Ph2PNHCH2-C4H3S)(eta(5)-C5Me5)Cl-2], 3, respectively. All new complexes were fully characterized by analytical and spectroscopic methods. H-1-P-31 NMR, H-1-C-13 HETCOR or H-1-H-1 COSY correlation experiments were used to confirm the spectral assignments. 1-3 are suitable catalyst precursors for the transfer hydrogenation of acetophenone derivatives. Notably [Ru(Ph2PNHCH2-C4H3S)(eta(6)-benzene) Cl-2], 1, acts as an excellent catalyst, giving the corresponding alcohols in 98-99% yields in 30 min at 82 degrees C (TOF <= 200 h(-1)) for the transfer hydrogenation reaction in comparison to analogous rhodium or iridium complexes. This transfer hydrogenation is characterized by low reversibility under these conditions. Copyright (C) 2011 John Wiley & Sons, Ltd. | en_US |
dc.description.sponsorship | Dicle University [DUAPK 05-FF-27] | en_US |
dc.description.sponsorship | Partial support from Dicle University (project number: DUAPK 05-FF-27) is gratefully acknowledged. | en_US |
dc.identifier.citation | Aydemir, M., Baysal, A. ve Turgut, Y. (2011). Applications of transition metal complexes containing aminophosphine ligand to transfer hydrogenation of ketones. Applied Organometallic Chemistry, 25(4), 270-275. | |
dc.identifier.doi | 10.1002/aoc.1753 | |
dc.identifier.endpage | 275 | en_US |
dc.identifier.issn | 0268-2605 | |
dc.identifier.issn | 1099-0739 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.scopus | 2-s2.0-79953032764 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 270 | en_US |
dc.identifier.uri | https://doi.org/10.1002/aoc.1753 | |
dc.identifier.uri | https://hdl.handle.net/11468/13959 | |
dc.identifier.uri | https://onlinelibrary.wiley.com/doi/epdf/10.1002/aoc.1753 | |
dc.identifier.volume | 25 | en_US |
dc.identifier.wos | WOS:000288806300004 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.institutionauthor | Aydemir, Murat | |
dc.institutionauthor | Baysal, Akın | |
dc.institutionauthor | Turgut, Yılmaz | |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Applied Organometallic Chemistry | |
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 | Transition metals | en_US |
dc.subject | Transfer hydrogenation | en_US |
dc.subject | Catalysis | en_US |
dc.title | Applications of transition metal complexes containing aminophosphine ligand to transfer hydrogenation of ketones | en_US |
dc.title | Applications of transition metal complexes containing aminophosphine ligand to transfer hydrogenation of ketones | |
dc.type | Article | en_US |
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