Novel N-Alkylbenzimidazole-Ruthenium (II) complexes: Synthesis and catalytic activity of N-alkylating reaction under solvent-free medium
dc.authorid | Özdemir, Namık/0000-0003-3371-9874 | |
dc.authorid | Gurbuz, Nevin/0000-0003-3201-3597 | |
dc.authorid | Özdemir, İsmail/0000-0001-6325-0216 | |
dc.authorwosid | Özdemir, Namık/J-6434-2015 | |
dc.authorwosid | Gurbuz, Nevin/A-3069-2016 | |
dc.authorwosid | ŞAHİN, Neslihan/F-6402-2019 | |
dc.authorwosid | Özdemir, İsmail/ABI-5192-2020 | |
dc.contributor.author | Sahin, Neslihan | |
dc.contributor.author | Ozdemir, Namik | |
dc.contributor.author | Gurbuz, Nevin | |
dc.contributor.author | Ozdemir, Ismail | |
dc.date.accessioned | 2024-08-04T20:45:37Z | |
dc.date.available | 2024-08-04T20:45:37Z | |
dc.date.issued | 2019 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | In this article, direct N-alkylation reactions of amines with alcohols derivatives have been investigated. For this purpose, a new series ruthenium (II) complexes bearing N-coordinated benzimidazole complexes with have been synthesized and fully characterized by elemental analysis, FT-IR, H-1 NMR and, C-13 NMR spectroscopies. Additionally, the structures of the complexes 2b and 2c have been confirmed by X-ray crystallography. Although the N-alkylating reaction is usually performed in toluene, the catalytic study of complexes 2a-d has carried out no additional solvent and alcohol acted both as solvent and reactant of alkylating by using a little excess of alcohols. Surprisingly, conversion and selectivity of amine product for alkylation reaction have been seen high in medium solvent-free relative to in toluene. | en_US |
dc.identifier.doi | 10.1002/aoc.4704 | |
dc.identifier.issn | 0268-2605 | |
dc.identifier.issn | 1099-0739 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopus | 2-s2.0-85058966222 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.uri | https://doi.org/10.1002/aoc.4704 | |
dc.identifier.uri | https://hdl.handle.net/11616/98586 | |
dc.identifier.volume | 33 | en_US |
dc.identifier.wos | WOS:000456252400003 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley | en_US |
dc.relation.ispartof | Applied 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 | catalysis | en_US |
dc.subject | crystal structure | en_US |
dc.subject | N-alkylation | en_US |
dc.subject | N-coordinated benzimidazole | en_US |
dc.subject | ruthenium | en_US |
dc.title | Novel N-Alkylbenzimidazole-Ruthenium (II) complexes: Synthesis and catalytic activity of N-alkylating reaction under solvent-free medium | en_US |
dc.type | Article | en_US |