Piano-stool benzothiazol-2-ylidene Ru(II) complexes for effective transfer hydrogenation of carbonyls
dc.contributor.author | Oruc, Zeynep Ipek | |
dc.contributor.author | Gok, Lutfiye | |
dc.contributor.author | Turkmen, Hayati | |
dc.contributor.author | Sahin, Onur | |
dc.contributor.author | Buyukgungor, Orhan | |
dc.contributor.author | Cetinkaya, Bekir | |
dc.date.accessioned | 2019-10-27T23:10:44Z | |
dc.date.available | 2019-10-27T23:10:44Z | |
dc.date.issued | 2016 | |
dc.department | Ege Üniversitesi | en_US |
dc.description.abstract | Benzothiazolium bromides (NSHC center dot HBr) (1a-j) with a variety of alkyl chain or benzyl substituents on N atom were prepared. The synthesis of ruthenium(II) (NSHC) complexes, (2a-j) could be achieved by in situ deprotonation of benzothiazolium salts with Ag2O and [RuCl2(p-cymene)](2). They were characterized by H-1, C-13, F-19 NMR, IR spectroscopy and elemental analysis. The molecular structures of 2d, 2e and 2g were ascertained by single-crystal X-ray diffraction studies. The catalytic properties of complexes, (2aej), with electron-donating or -withdrawing groups were investigated in transfer hydrogenation (TH) of ketones, and aldehydes with good to excellent yields. The presence of the CH2(CH2)(16)CH3 or CH2C6F5 on the N atom of the benzothiazol-2-ylidene complexes (2g, 2j) showed the highest activity for TH reaction. The catalytic properties of the N-alkyl substituted ruthenium(II) (NSHC) complexes(2h-j) may be interpreted by micelle effects. (C) 2016 Elsevier B.V. All rights reserved. | en_US |
dc.description.sponsorship | Ege UniversityEge University [2011-FEN-091] | en_US |
dc.description.sponsorship | Financial support from Ege University (Project 2011-FEN-091) is gratefully acknowledged. | en_US |
dc.identifier.doi | 10.1016/j.jorganchem.2016.02.003 | |
dc.identifier.endpage | 44 | en_US |
dc.identifier.issn | 0022-328X | |
dc.identifier.issn | 1872-8561 | |
dc.identifier.issn | 0022-328X | en_US |
dc.identifier.issn | 1872-8561 | en_US |
dc.identifier.scopusquality | Q3 | en_US |
dc.identifier.startpage | 36 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.jorganchem.2016.02.003 | |
dc.identifier.uri | https://hdl.handle.net/11454/52950 | |
dc.identifier.volume | 807 | en_US |
dc.identifier.wos | WOS:000371345800006 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier Science Sa | en_US |
dc.relation.ispartof | Journal of Organometallic Chemistry | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Benzothiazolium salts | en_US |
dc.subject | NSHC-Ru(II) complexes | en_US |
dc.subject | The transfer hydrogenation | en_US |
dc.subject | Catalysis | en_US |
dc.title | Piano-stool benzothiazol-2-ylidene Ru(II) complexes for effective transfer hydrogenation of carbonyls | en_US |
dc.type | Article | en_US |