New (carbene)ruthenium-arene complexes: Preparation and uses in catalytic synthesis of furans
dc.authorid | KUCUKBAY, HASAN/0000-0002-7180-9486 | |
dc.authorid | Cetinkaya, Bekir/0000-0002-4551-8650 | |
dc.authorwosid | KUCUKBAY, HASAN/A-5050-2019 | |
dc.contributor.author | Kucukbay, H | |
dc.contributor.author | Cetinkaya, B | |
dc.contributor.author | Guesmi, S | |
dc.contributor.author | Dixneuf, PH | |
dc.date.accessioned | 2024-08-04T20:13:18Z | |
dc.date.available | 2024-08-04T20:13:18Z | |
dc.date.issued | 1996 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | A variety of neutral ruthenium-carbene complexes RuCl2(carbene)(arene) 1 (carbene=C(NR)C6H4(NR), R=Me (a), Et (b); arene=p-Me-C6H4-Pr-i (1), C(6)H(3)Me(3) (2), C(6)Me(6) (3)) have been prepared by reaction of [RuCl2(arene)](2) precursors with the enetetraamines (RN)C6H4(RN)C=C(NR)C6H4(NR) I (R=Me) and II (R=Et). Ru=C(NCH(2)Ph)CH2CH2(NCH(2)Ph)Cl-2(p-cymene) (4) was prepared similarly, whereas the reaction of [RuCl2-(cycloocta-1,5-diene)](n) with I led to the formation of the 16-electron neutral complex RuCl2[=C(NMe)C6H4(NMe)](3) (6). One of them (3a) was transformed into the dihydride derivative RuH2(C(NMe)C(6)H(4)NMe)(C(6)Me(6)) (5). The cyclic voltammograms of derivatives 1-3 show that they are oxidized in the range E(1/2)=1.03-1.31 V vs SCE and are more electrophilic than the isoelectronic RuCl2(PR(3))(arene) complexes. Derivatives 1a, 3a, and 3b act as efficient catalyst precursors for the electrophilic activation of the C=C bond of (Z)-3-methylpent-2-en-4-yn-1-ol to afford 2,3-dimethylfuran in good yield via intramolecular cyclization. | en_US |
dc.identifier.doi | 10.1021/om960002l | |
dc.identifier.endpage | 2439 | en_US |
dc.identifier.issn | 0276-7333 | |
dc.identifier.issue | 10 | en_US |
dc.identifier.scopus | 2-s2.0-0037533722 | en_US |
dc.identifier.scopusquality | N/A | en_US |
dc.identifier.startpage | 2434 | en_US |
dc.identifier.uri | https://doi.org/10.1021/om960002l | |
dc.identifier.uri | https://hdl.handle.net/11616/93522 | |
dc.identifier.volume | 15 | en_US |
dc.identifier.wos | WOS:A1996UL32100006 | en_US |
dc.identifier.wosquality | N/A | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Amer Chemical Soc | en_US |
dc.relation.ispartof | Organometallics | 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 | Opening Metathesis Polymerization | en_US |
dc.subject | Terminal Alkynes | en_US |
dc.subject | Ruthenium Complexes | en_US |
dc.subject | Reconstitutive Condensation | en_US |
dc.subject | Carbon-Dioxide | en_US |
dc.subject | Enol Esters | en_US |
dc.subject | One-Step | en_US |
dc.subject | Derivatives | en_US |
dc.subject | Alkenes | en_US |
dc.subject | Cyclopropanation | en_US |
dc.title | New (carbene)ruthenium-arene complexes: Preparation and uses in catalytic synthesis of furans | en_US |
dc.type | Article | en_US |