Catalytic activity in transfer hydrogenation using ruthenium (II) carbonyl complexes containing two 1,8-naphthyridine as N-monodentate ligands

Gajardo, Juana; Araya, Juan Carlos; Ibañez, Andres; Guerchais,Veronique; Le Bozec , Hubert; Moya, Sergio A; Aguirre Pedro

Keywords: Ruthenium (II) 1,8-Naphthyridine complexes, Transfer hydrogenation Acetophenone, Homogeneous catalysis

Abstract

A new series of novel complexes of type cis-[Ru(CO)2Cl2(L)2], L=2-phenyl-1,8-naphthyridine, 2-(4′-nitrophenyl)- 1,8-naphthyridine, 2-(4′-bromophenyl)-1,8-naphthyridine, 2-(4′-methylphenyl)-1,8-naphthyridine, 2-(3′-methoxyphenyl)-1,8-naphthyridine, 2-(2′-methoxyphenyl)-1,8-naphthyridine and 2-(4′methoxyphenyl)- 1,8-naphthyridine have been successfully synthesized and characterized. We found that the complexes can be directly synthesized from [RuCl2(CO)2]2 with high yield. The crystallographic structures of complex cis- [RuCl2(CO)2(2-(4′-methoxyphenyl)-1,8-naphthyridine-κN8)2] and cis-[RuCl2(CO)2(2-(2′-methoxyphenyl)-1,8- naphthyridine-κN8)2] have been established by X-ray single crystal diffraction studies, which indicate an octahedral geometry with two 1,8-naphthyridine ligands coordinated to the metal in a N-monodentate fashion. The ruthenium(II) complexes have been studied as catalysts in the transfer hydrogenation of acetophenone. We found that complexes show moderate activities and a 100% selectivity. The best turnover frequency (390 h−1) is found for cis-[RuCl2(CO)2(2-(4′-methoxyphenyl)-1,8-naphthyridine-κN8)2] when the substrate/catalysis ratio was 1000/1. The catalytic conditions were optimized using different substrate/catalyst and base/catalyst ratios.

Más información

Título de la Revista: INORGANICA CHIMICA ACTA
Volumen: 486
Editorial: ELSEVIER SCIENCE SA
Fecha de publicación: 2019
Página de inicio: 129
Página final: 134
Idioma: english
Financiamiento/Sponsor: FONDECYT
URL: https://www.journals.elsevier.com/inorganica-chimica-acta
DOI:

https://doi.org/10.1016/j.ica.2018.10.037

Notas: ISI, SCOPUS