Catechol-type ligand containing new modular design dioxaborinane compounds: Use in the transfer hydrogenation of various ketones
dc.contributor.author | Kilic, Ahmet | |
dc.contributor.author | Kaya, Ibrahim Halil | |
dc.contributor.author | Ozaslan, Ismail | |
dc.contributor.author | Aydemir, Murat | |
dc.contributor.author | Durap, Feyyaz | |
dc.date.accessioned | 2024-04-24T16:11:00Z | |
dc.date.available | 2024-04-24T16:11:00Z | |
dc.date.issued | 2018 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | A novel class of tricoordinate dioxaborinane compounds, which have the general formula [B-1(L1-5)] and [B-2(L1-5)], were designed and synthesized by the corresponding catechol-type ligands (L-1-L-5) at ambient temperature. All the new compounds were fully characterized by NMR (H-1, C-13, and B-11), FT-IR, UV-vis, LC-MS spectroscopy, and melting point analysis and microanalysis. The dioxaborinane [B-1(L1-5)] and [B-2(L1-5)] compounds were investigated as catalyst for the transfer hydrogenation of various ketones under suitable conditions. Particularly, it was proved that the ferrocene-based dioxaborinane [B-1(L1-5)] molecules can afford an efficient catalytic conversion compared to corresponding 3,5-bis(trifluoromethyl)phenyl-based [B-2(L1-5)] dioxaborinanes in transfer hydrogenation catalytic studies. | en_US |
dc.description.sponsorship | TUBITAK [113Z297]; Harran University; Dicle University [FEN.17.019] | en_US |
dc.description.sponsorship | Support from TUBITAK (Project number: 113Z297) is gratefully acknowledged. In addition, partial supports of this work by Harran University and Dicle University (Project number: FEN.17.019) are gratefully acknowledged. | en_US |
dc.identifier.doi | 10.1016/j.catcom.2018.03.023 | |
dc.identifier.endpage | 46 | en_US |
dc.identifier.issn | 1566-7367 | |
dc.identifier.issn | 1873-3905 | |
dc.identifier.scopus | 2-s2.0-85044934239 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 42 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.catcom.2018.03.023 | |
dc.identifier.uri | https://hdl.handle.net/11468/15224 | |
dc.identifier.volume | 111 | en_US |
dc.identifier.wos | WOS:000433266800009 | |
dc.identifier.wosquality | Q2 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Bv | en_US |
dc.relation.ispartof | Catalysis Communications | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Catechol-Type Ligands | en_US |
dc.subject | Dioxaborinanes | en_US |
dc.subject | Spectroscopy | en_US |
dc.subject | Transfer Hydrogenation | en_US |
dc.subject | Ketones | en_US |
dc.title | Catechol-type ligand containing new modular design dioxaborinane compounds: Use in the transfer hydrogenation of various ketones | en_US |
dc.title | Catechol-type ligand containing new modular design dioxaborinane compounds: Use in the transfer hydrogenation of various ketones | |
dc.type | Article | en_US |