Dergi makalesi Açık Erişim
Gok, Yasar; Aykut, Irem Tutkum; Gok, Halil Zeki
{ "@context": "https://schema.org/", "@id": 5553, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "affiliation": "Burdur Mehmet Akif Ersoy Univ, Bucak Fac Technol, Dept Biomed Engn, TR-15300 Bucak, Burdur, Turkey", "name": "Gok, Yasar" }, { "@type": "Person", "affiliation": "Burdur Mehmet Akif Ersoy Univ, Bucak Fac Technol, Dept Biomed Engn, TR-15300 Bucak, Burdur, Turkey", "name": "Aykut, Irem Tutkum" }, { "@type": "Person", "affiliation": "Burdur Mehmet Akif Ersoy Univ, Bucak Fac Technol, Dept Biomed Engn, TR-15300 Bucak, Burdur, Turkey", "name": "Gok, Halil Zeki" } ], "datePublished": "2020-01-01", "description": "The main objective of this study is to develop readily accessible and recyclable solid catalysts for enantioselective reactions. To achieve this, magnetic MCM-41 and non-magnetic SBA-15 mesoporous supports were prepared, then mesoporous silica supported chiral urea-amine bifunctional catalysts were synthesized by grafting of chiral urea-amine ligand onto SBA-15 and magnetic MCM-41. The magnetic and non-magnetic supports and so-prepared solid catalysts were characterized by using different methods such as N(2)sorption measurements, Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscope-energy dispersive X-ray analysis (FESEM-EDX), X-ray diffraction (XRD), and thermogravimetric analysis (TGA). Results showed that (1R, 2R) or (1S, 2S)-1,2-diphenylethane-1,2-diamine was successively immobilized onto magnetic MCM-41 and SBA-15 pores. The heterogeneous chiral solid catalysts and their homogenous counterparts exhibited high activities both enantioselective transfer hydrogenation reaction (up to 99% conversion and 65%ee) and enantioselective Michael reaction (up to 98% conversion and 26%ee). Moreover, the SBA-15 supported solid catalysts were separated from the reaction mixture by simple filtration, whereas the magnetic MCM-41 supported solid catalysts were separated by simple magnetic decantation and reused in three consecutive catalytic experiments.", "headline": "Readily accessible mesoporous silica nanoparticles supported chiral urea-amine bifunctional catalysts for enantioselective reactions", "identifier": 5553, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Readily accessible mesoporous silica nanoparticles supported chiral urea-amine bifunctional catalysts for enantioselective reactions", "url": "https://aperta.ulakbim.gov.tr/record/5553" }
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