Dergi makalesi Açık Erişim
Yilmaz, Mustafa Kemal; Keles, Huelya; Ince, Simay; Keles, Mustafa
{ "@context": "https://schema.org/", "@id": 33829, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "affiliation": "Mersin Univ, Fac Arts & Sci, Dept Chem, TR-33343 Mersin, Turkey", "name": "Yilmaz, Mustafa Kemal" }, { "@type": "Person", "affiliation": "Osmaniye Korkut Ata Univ, Fac Arts & Sci, Dept Chem, TR-80000 Osmaniye, Turkey", "name": "Keles, Huelya" }, { "@type": "Person", "affiliation": "Osmaniye Korkut Ata Univ, Fac Arts & Sci, Dept Chem, TR-80000 Osmaniye, Turkey", "name": "Ince, Simay" }, { "@type": "Person", "affiliation": "Osmaniye Korkut Ata Univ, Fac Arts & Sci, Dept Chem, TR-80000 Osmaniye, Turkey", "name": "Keles, Mustafa" } ], "datePublished": "2018-01-01", "description": "Three iminophosphine ligands having soft phosphorus and hard nitrogen atoms and their Pd(II) complexes were synthesized and characterized using H-1 NMR, C-13 NMR, P-31 NMR and Fourier transform infrared spectroscopic techniques. Also, electrochemical properties of the iminophosphines and their Pd(II) complexes were investigated in acetonitrile-tetrabutylammonium perchlorate solution with cyclic and square wave voltammetry techniques. All Pd(II) complexes were evaluated as catalysts for carbonylative cross-coupling reactions of aryl iodides with phenylboronic acid. The Suzuki carbonylation of aryl iodides at 80 degrees C under balloon pressure of carbon monoxide in the presence of K2CO3 as a base was examined, and good to high conversions and excellent selectivities were obtained.", "headline": "Iminophosphine palladium catalysts for Suzuki carbonylative coupling reaction", "identifier": 33829, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Iminophosphine palladium catalysts for Suzuki carbonylative coupling reaction", "url": "https://aperta.ulakbim.gov.tr/record/33829" }
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