Issue 25, 2021

Half-sandwich Ru(ii) arene complexes bearing benzimidazole ligands for the N-alkylation reaction of aniline with alcohols in a solvent-free medium

Abstract

In 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, 1H NMR and 13C 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.

Graphical abstract: Half-sandwich Ru(ii) arene complexes bearing benzimidazole ligands for the N-alkylation reaction of aniline with alcohols in a solvent-free medium

Supplementary files

Article information

Article type
Paper
Submitted
29 Mar 2021
Accepted
11 May 2021
First published
13 May 2021

New J. Chem., 2021,45, 11075-11085

Half-sandwich Ru(II) arene complexes bearing benzimidazole ligands for the N-alkylation reaction of aniline with alcohols in a solvent-free medium

M. Çiçek, N. Gürbüz, N. Özdemir, İ. Özdemir and E. İspir, New J. Chem., 2021, 45, 11075 DOI: 10.1039/D1NJ01539G

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