Cicek, MetinGurbuz, NevinOzdemir, NamikOzdemir, IsmailIspir, Esin2024-08-042024-08-0420211144-05461369-9261https://doi.org/10.1039/d1nj01539ghttps://hdl.handle.net/11616/100009In this article, the direct N-alkylation reactions of amines with alcohol derivatives using the borrowing hydrogen methodology have been investigated. For this purpose, a new series of half-sandwich ruthenium(II) complexes bearing N-coordinated benzimidazole complexes have been synthesized and fully characterized by FT-IR, H-1 NMR and C-13 NMR spectroscopies. Additionally, the structures of the complexes 2a-2e have been characterized by X-ray crystallography. ALL new complexes were investigated for their catalytic activities in the alkylation reaction of amines with alcohol derivatives. It was found that alkylation reactions in a solvent-free medium are efficient and selective.eninfo:eu-repo/semantics/closedAccessRuthenium(Ii) ComplexesCatalytic EfficiencyHydrogen-TransferSecondary-AminesDiscoveryOxidationAminationIminesHalf-sandwich Ru(II) arene complexes bearing benzimidazole ligands for the N-alkylation reaction of aniline with alcohols in a solvent-free mediumArticle4525110751108510.1039/d1nj01539g2-s2.0-85108881742Q2WOS:000658013400001Q2