Aminophosphine-palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions
dc.contributor.author | Aydemir, Murat | |
dc.contributor.author | Baysal, Akin | |
dc.contributor.author | Sahin, Ertan | |
dc.contributor.author | Gumgum, Bahattin | |
dc.contributor.author | Ozkar, Saim | |
dc.date.accessioned | 2024-04-24T16:14:52Z | |
dc.date.available | 2024-04-24T16:14:52Z | |
dc.date.issued | 2011 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Reaction of furfurylamine with 1 or 2 equivalents of PPh2Cl in the presence of Et3N, proceeds under anaerobic conditions in thf to give furfuryl-2-(N-diphenylphosphino)amine, Ph2PNHCH2-C4H3O, 1 and furfuryl-2-(N,N-bis(diphenylphosphino)amine), (Ph2P)(2)NCH2-C4H3O, 2, respectively. The reactions of 1 and 2 with MCl2(cod) (M = Pd, Pt; cod = 1,5-cyclooctadiene) or Pt(CH3)(2)(cod) yield complexes [M(Ph2PNHCH2-C4H3O)(2)Cl-2] (M= Pd 1a, Pt 1b), [Pt(Ph2PNHCH2-C4H3O)(2)(CH3)(2)] (1c), and [M((Ph2P)(2) NCH2-C4H3O)Cl-2] (M= Pd 2a, Pt 2b), [Pt((Ph2P)(2)NCH2-C4H3O)(CH3)(2)] (2c), respectively. All the compounds were isolated as analytically pure substances and characterized by NMR, IR spectroscopy and elemental analysis. Representative solid-state structures of 2a and 2b were also determined by X-ray single crystal diffraction technique. Furthermore, the palladium complexes 1a and 2a were tested and found to be highly active catalysts in the Suzuki coupling and Heck reaction affording biphenyls and trans-stilbenes, respectively. (C) 2011 Elsevier B.V. All rights reserved. | en_US |
dc.description.sponsorship | Dicle University [DUAPK 05-FF-27]; Turkish Academy of Sciences | en_US |
dc.description.sponsorship | Partial support from Dicle University (Project No.: DUAPK 05-FF-27) and Turkish Academy of Sciences is gratefully acknowledged. | en_US |
dc.identifier.doi | 10.1016/j.ica.2011.07.056 | |
dc.identifier.endpage | 18 | en_US |
dc.identifier.issn | 0020-1693 | |
dc.identifier.issn | 1873-3255 | |
dc.identifier.issue | 1 | en_US |
dc.identifier.scopus | 2-s2.0-80054987666 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 10 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.ica.2011.07.056 | |
dc.identifier.uri | https://hdl.handle.net/11468/15455 | |
dc.identifier.volume | 378 | en_US |
dc.identifier.wos | WOS:000296538000002 | |
dc.identifier.wosquality | Q3 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Sa | en_US |
dc.relation.ispartof | Inorganica Chimica Acta | |
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 | Furfurylamine | en_US |
dc.subject | Palladium | en_US |
dc.subject | Platinum | en_US |
dc.subject | Heck Reaction | en_US |
dc.subject | Suzuki Coupling | en_US |
dc.title | Aminophosphine-palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions | en_US |
dc.title | Aminophosphine-palladium(II) complexes: Synthsesis, structure and applications in Suzuki and Heck cross-coupling reactions | |
dc.type | Article | en_US |